SCIENTIFIC ABSTRACT VASILYEV, L.L. - VASILYEV, L.S..

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001858910004-5
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: August 31, 2001
• Sequence Number: 4
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

VASILIYV,V, L.L.; SOSNOVSKAYA, Z.A.
~---fi,od"e-o'i fnetors affecting the centrnl nervous system in the course of
a pnrnbiotic process in the heart. Trudy Inst. fiz3ol. 6:18-23 157.
(MIRA 11:4)
1. Laboratoriya obshchey nervno-myshechnoy fiziologii (znveduyushchiy
L.L. Vneillyev).
(BRAIN) (HEART)

USSR/Human and Animal Physiology (Normal and Patholo(4ical) T
Nervous System. General Problems.
Abs Jour : Ref Zhur Biol., No 6, 1959, 26948
Author : Vasil'yev, L.L.
Inst : Institute of Experimental Medicine, AS Latvian SSR
Title : On Pathogenesis and Therapy of Nervous Diseases in the
Light of Contemporary Concepts of Parabiosis.
Orig Bib ; Tr. In-ta eksperim. med. AN Latv.SSR, 1957, 13, 217-225
Abstract : Two phases of inhibition in the development of parabiotic
process were discovered: I - electro-positive, in which
the inhibition of excitability and condL,.ctivity is con-
nected with the increase of functional mobility, and II -
electro-negative, which is characterized by progressing
decrease of lability. The I phase Is regarded as an ex-
pression of tissue adaptation to long-lasting alterating
Card 1/2

USM/Human and Animal Physiology (Normal and Pathological) T
Neuro-Muscular Physiology.
Abs Jour : Ref Zhur Biol., No 6, 1959, 26930
Aothor : Vasil'yev, L.L.
Inst : Kiev University
Title : Experiment of Quantitative Evaluation of Nerve Adapta-
tion to Parabiotizing Action of a Direct Current Catho-
de
Orig Pub : Nauk. zap. Kiewsk. LM-t, 1957, 16, No 17, 113-43
Abstract : The experiments were conducted on intact neuro-muscular
specimens (sciatic nerve-gastrocnemic mvscle) taken
from different frogs. The method of "minimum polariza-
tion of nerve" was utilized. After having induced, in
the part of nerve which is on the cathode, the state of
parabiotic noncond,,,ctivity by means of letting through
Card 1/3
?

USSR/Human and Animal Physiology (Normal and Pathological) T
Neuro-Muscular Physiology.
Abs Jour Ref Zhur Biol.,.No 6, 1959, 26930
"the constant of slope" a decreased and "the constant
of level" b fell to zero. Exporiments with nerves
enriched by Ca gave the opposite result. Constants a
and b. which determine the ca-arse of hyperbolic curve
of thre6hhold cathode parabiosi6, nay truly serve as
quantitative index of nerve adaptation to parabiotizing
action of a cathode. -- F.I. Mumladze
0
Card 3/3

fir
BIAGWAtOVA. Ye.T.; VASIL, Ymy'..
Affect of amytal and chloral hydrate anesthesia on the anti-
parabiotic activity of nerve centers [vith an ry in Anglishl.
-liziol.zhur. 43 no.9:842-860 S 157. (MIRA 10411)
,-; "' - r'-, .A. ~
1. Isboratoriya obahchey nervno-myshechnoy fiziologii Inatituts
fiziologii im. I.P.Pavlova AN SSSR, Leningrad.
(NERVIC MUSCLE PRIPARATION,
parabiosis, eff. pmobarbital & chloral hydrate
annath. (Rua))
~AMOBARBITAL, anesthesia and analgesia,
eff. on parabiosis in nerve-musc. prep. (Rua))
(CHLORAL HYDRATE, anesthesia and analgesia,
same)

A
A*M UOSR / Human and Animal Physiology 'Normal and Pathological). T
Neuromuscular Physiology.
Abe Jour : Ref Zhur - Biologlya, No 13, 1958, No. 60680
Author : Vasillyev, L. L.
Inst : Leningrad Tt-al-e University
Title : Tho Simultaneous Effect of Lesion-Producing Agonto on
the Specific and Non-Specific Reactivity of tho Nervo
Orig Pub ! Uch. zap. IGU, 1957, No 222, 38-48
Abstract : The local effect of an antil3enic (horse) serum W on
the sciatic nerve (nouromuscular preparation) in the
region of threshold cathode parabiosis was tested. In
thirteen tests done on the preparation from sensitized
frogs, seven showed a noticeable drop in the level of
the curve on the threshold parablocis (ICTF) when it was
put on the cathode part of the nerve. The drop mostly
began inmediately after S application, and sometiinas I - 5
A,
Card 1/2 LJ-e~-01-0- x ' ) t- j1~A
/Ialpf -~t -&

U3-1~'R / Human and Animal Phy8 iology (Normal and Pathological). T
Neuro=scular Physiology.
Abs Jour Ref Zhur - Biologiya, No 13, 1958, No. 6c68o
minutes later. In control tests, there was no lavering
of ICTP under the effect of S. Consequently, the local
anaphylactic effect of S on the nerve was added to the
parabiotic effect of the cathode. The lowering of LCTP
was also obtained when S was applied to the exposed
interstitial brain. In a series of teats, the threshold
cathode parabiosis was produced in the part of the nerve
which was connected both to the mu3cles and to the brain.
In =at of these tests done on sinsitized frogs, after
the administration of decisive dooea of S there occurred
a sufficiently well expressed lowering of the LCTP. In
this way, in all the described cases the parabiotic state
of the nerve part, produced and kept at the threshold
level, becaly, deepened. -- F. 1. tvaimladze
Card 2/2
115

WSIL-YILV, L. L. (Prof. Dr.) 11"orr. Mlbr. Aca-1. Vied'. So-'. lu~
"Atmospheric Ions and Health," Punjab Mod. Journal, Vol. VII, No. 7, Feb.
58.

VASIL'YEV, Leonid Leonidovich, prof.; FILIPPOV, L., red.; TROYANOVSEAYA,
~iltadv .........-
*I
(Mysterious phenomena of the human psyche] Tainstvannye lavloniia
chelovecheskoi psikhIki. Moskva, Gos.izd-vo polit.lit-ry, 1959.
118 P. (MIRA.12:11)
1. Chlen-korrespondent Akademii meditainakikh nauk (for Vasil'yev).
(Psychology. Physiological)

MYASISHCHRV, Vladimir Nikolayevich, prof., red.; KHVILIVITSKIY,
Toodor Yakovlevich, starshiy nauchnyy sotrudnik, red.;
GRASHCHNNKOV, N.L. Prof., red.: ANAWYEV, B.G., prof.. red.;
VASjjLYIM,_L.L_q._prof., red.; GILYAROVSKIY, V.A., prof., red.
-rd-eceased]; OMOROKOV, L.I., prof., zasluzhann deyatell nauki,
red.; PROTOPOPOV. V.P., prof., red. Edecessedf-, BEMMOLIT,
Z,M,, red.; RULSVA, H.S., tekhn.red.
EV.M.Bekhterev and modern problems in the structure and function
of the brain under normal and pathological conditions; transactions
of the All-Union Conference in Honor of the 100th AnniverEary of
V.M.Bekliterevle Birth] V.M.Bekhterev i sovremennye problemy stroe-
niia i funktaii mozga v norme i patologii; trudy VSOSOiU2noi
konferentsii, posviashchennoi atoletiiu so dnia rozhdeniia V.M.
Bekhtereva. Pod red. V.N.Miasishcheva i T.IA.Khvilivitskogo.
Leningrad, Gos.12d-vo med.lit-ry Medgiz, Leningr.otd-nie, 1959.
294 p. (MIRA 14:2)
(Continued on next card)

KYASISHCHEV. V.N.---(continued) Card 2.
1. Chlea-korrespondent Akadenii pedagogiches"Ich nauk RSFsa (for
Myosishchav). 2,1'redsedstall Uchenogo moditainakogo saveta
Ministerstva zdravookhrananiya SSSR. chlen-korrenondeat AN SWR
i daystvitellnyy chlen AMU SM (for Graahche&.ov). 3. Doyetvi-
talInyy chlen Akademii pedagogicheakikh nauk RSFSR (for Anan'yev).
4. Chlon-korrespondent AMU SSSR (for Vasillyev). 5. Deystvitellnyy
chlen ARN SSSR (for Gilyarovskiy). 6. Doyi3tvitallnyy chlea AN USSR
(for Protopopov).
(mmyous SYSTM)
RM, VLADIHM KIKHAILOVICH, 1857-1927)

VASILITKV. L.1.
Adaptation and seusitatIzation of the neural formations during
the development of parabiosis (steady excitation) in them. Trudy
Iuet.fiziol. 81368-376 159. (MIRA 1315)
1. laboratorlya ner7no-myshechnoy fiziologit (zaveduyashchiy -
L.L. Vasillyev) Institute, fiziologli im. I.P. Pavlova AN SSSR.
(MMVOUS STSTIKX)

VASIL17EV, prof.; BUIATOV, P.K., prof.
Review of A.A.Minkh's book "Ionization of air and Its significance
for health." Vest.AJW SSSR 14 no.8:86-87 '59. (MIRA 12:11)
1. Chlan-korrespondent AMN SSUR.
(AIR, IONIZO) (Kim, A.A.)
0

VASIL' YLOV, L.L.
Biametric meth(x1a in nourann ocular physiolog7. Vest.WU 14
no.9:153-159 '59. (MIRA 12:5)
(BI014BTRY) (ELECTROPHYSIOLOGY)

VASIL'YYjV, L.L.; SOSIKWSKATA, Z.A.
-~'- ~Parabiotic and "deparabiotic" influoncen of the central nervous
system on the heart. Veat.IjCrU 14 no.21:li6-121 '5 9.
(MIRK 12:10)
(nART ) (BRAIN) (PARABIOSIS)

.VASILIYEV. L. L.
PHASE I BOOK EXPLOITATION SOV/6150
Akademiya nauk Latviyskoy SSR. institut eksperimentallnoy
meditsiny,
Voprosy kurortologii. [t.] 5: Problemy fiziologicheskogo deystviya.
i terapevticheskrigo primenenlya aeroionov (Problems in Health-
Resort Therapy. V. 5: Studiesof the Physiologi6al Effect and Ther-
apeutic Application of Air Tons). Riga, lzd-v'o AN Latviyskoy
SSR,, 1.959. 424 p. (Series: Its: Trudy, t. 20) Errata slip in-
serted. 1000 copies printed.
Sponsoring Ageney: Akademiya nauk Latviyskoy SSR. Institut eksperi-
nentallnoy meditsiny.
T
Editorial Board: Resp. ~d. I.J. L. Vasillypy, Professor, P. D. Perli
Professor, F. Ux. Portnov, Candidate of Medical Sciences, Ya. Yu.
Reynet,, Candidate of Physical and Mathematical Sciences, and L.M.
Tutkevich, Candidate of Medical Sciences; Ed.: A. Vengranovich;
Tech. Ed.: A. Zhukovska-ya.
Card qC4P /_3

Problems in Health-Resort (-'_font. )
SOV/6150
PURPOSE: This bo-k is intended for physicians working at health
res,~,rts and for tha- genc-ral practitioner.
COVERAGE: This a ';cilection of articles, is essentially the
proceedings of the Sec~-jnd Conference on the Physiological Effect
and Therapeutic Applioation of Air lons; held at Riga (Latvian
SSR) In December 1957. The use of negative air ions ~is believed
to be beneficial in the treatment of nonhealln&wouncts and ulcers
which often result from radiation injury. The book coohtains
ph~)tou of nxmerru~3 devi--.es described intixetaxt. Numerou~s refer-
ences, mostly Soviet, are given at the edd of some of the articles.
TAKE OF CODMENTS [Abridged]:
Gerke, P. )-ra. -"Introduction 3
asil.'yev, L L ' 1.:urrent Problemo of the Physiological
v_~_` _* r-S,
c
_afA~_TtM1-apP,6Uv Effect of Aiv Tons 5
Card 2/0
'3

Problems in Health-Resort (Cont.) sov/6150
Raudam, E. I. and Ya. Yu. Reynet. The Effect of
Ionized Oxygen Upon Some Functions of the Organ-
-ism 231
[The article5 whose titles are here omitted deal with
the effe,ct of ionized air upon the exchange of gases in
hypertonic and thyrotoxic patients, the air-ion effect
in treatment of endoarteritis, bronchial asthmax
atrophic rhinitis, eczema, and neurodermatitis, and with
the treatment of nonhealing wounds with ionized oxygen] 241
Resolution of the Conference on the Physiological Effect
and Therapeutic Application of Air Ions 405
(~Vasillyev L L Problems of Air Ionization in the
_ ~~' ~ Y
of America 409
AVAILABLE: Library of Congress
SUBJECT: Biclogy and Medicine
IS/wb/bc
Card 2-19-63

XMIMILEY, L.L., prof.; BULATOT, P.K., prof., nsuchnyy red.; TOROBIM.
G#i-.-,--r-4iizd-va; GURDZHIIBU, A.Me', tekhn.red.
[Influencq of atmospheric ions on the body] TlHanis atmosfornykh
ionov na organim. Leningrad, (Yb-vo po rasprostraneniiu polit.
i nauchu.nanii FMSRo Leningrotd-niel 1960. 55 P.
(NDU 1433)
1. Chlen-korrespondent ANN SSSR (for Vasillyev).
Uir, Ionized)

ANFILOV, Gleb; ASRATYAN, B.A.; GULYAYN, P.I., doktor biol.nauk;
LIVAUOT, M.N., prof.; KWZKER, L.P., Icand.tekhn.nauk;
Y~~ILIYW, L.L.; IMYATSKIN, I.', kand.takhn.nauk
Is'thought transference possible? Opinions of Soviet
scientists. Znan. eila 35 no. 12:18-23 D 160. (MLRA 13:12)
(Thought transference)

VASILIYEN, Leonid Leonidovich; BLAGODATOVA, Yelena Tomasovna; SMSIODPIOV,
red. izd-vi-j--WROKINA, V.A., tekhx. red,
[Central influences eliminating or intensifying parabiosisl TSentrall-
rWe vliianiia~ ustraniaiushchie i uglubliaiushchie parabioz. Moakva,,
Izd-vo Akad. nauk SSSR, 1961. 92 P;) (MIRA 14:11)
1 (IIEM

VASIL119- ~L.-
--- -- #-L
Cbaracteristice of the stimulating action of arrhthymic (group)
stimuli. Trudy 1-go MMI 11:69-73 161. OC?A 15:5)
1. Kafedra fiziologii cheloveka i 2hitrotnylch (2av. - prof. L.L.Vasillev)
Leningradakogo gosudarstvennogo universiteta.
(NERVOUS SYSTEM)

I
.VASILIYEV. L.L.J, prof.
Experiments in psychomagnetism. Nauka i zhiznl 28 no.7:80-82 J1
161. OURA 14-8)
1. Leningradskiy universitet.
(MAGNETISH-PHYSIOLOGICAL EFFECT)

VASILIYEV, L.L.
Mechanisms of central influences eliminating parabiosis. Trudy
Len. ob-va est. 72 no.1:18-23 '61. (KRA 1l:;:3)
..4
(NERVOUS SYSTEM)

-VAI'I;IIIIy*?Iv$ L.L.; MIATKIN.-i, 14.11.
----- --- I-.- - --
Role of inhibition in Ue development of futi.?ui in ta-za
musculnr work, Nerv sist (Leningrad) 2 no,3jI:)2-15') '02.
OINI~
1. Kafedra fiziologii cliclovaka I zlilvotriyki, FLzIoIogIcIic:jkog,-)
InkitAtuta impni Ukhtorpskogo Le-ningradoxcgo jrc,~,udarstvennng,()
univornitata,

=1, A. V. ; V P.71 1J, "MV, L. L. )' '--,H AIF; I'UT
"A aLe t Lod fo r s o-j L d e na~ t ic) r. c f al Ir--- rs:.-e r,~
,- to :-(;0G K, 11
conductors civer the temrerature range -L(j
report submitted for 3rd Symp on Thermophysical Properties, Purdue IJIiv, Lufayette,
22-25 Mar 67~.

na

VERMIN, Nikita Nikolayevich; DIYAKONOVA-SAVELIYEVA, Ye.N., red.;
VASIL'YEV, L.L., IVPJiC'I, A Vred.; KOLOSOV, H.G., red.;
MAKAROV, P.O., red.# POLKAIIOV, A:A:,I red. (deceased]; POIXAMSKIY,
YU.I., red.; STEPAIMV, D.L., red.; SHVETSOVA, E.M., rod.;
YASHCHURZHIIISKAYA, A.B., tekhn. red.
(Cretaceous sediments in the northern part of the Fergana Valley
and their oil potential) Melovye otlozheniia severs. Ferganskoi
vpadiny i ikh neftenosnost'. Leningrad, Gostoptekhizdat,
1963. 219 p. (Leningradskoe obshchestvo estestvoispytatelei.
Trudy, vol. 70, no.2). (MIRA 16:12)

VASILIYEVI L.L.; SOSVOVSKAYA, Z.A.
Effect of stimulating impulses on inhibition foci in the spinal
cord. Trudy Inst. fiziol. 101284-293 t62 (MM 1713)
.1.. 1. Laboratoriya obshchey nervno-myshechnoy fiziologii (.zav.-
L.L.Vasillyev) Instituts. fiziologii imeni Favlova AN SSSR,

VASIL'YEV L L , prof.; KOLITSOVA, M.M., red.; RULEVA, M.S.,
tekhn. red.
[Significance of N.E.Vvedenskii's physiological theory for
,ouropathology] Znachenie fixiologicheskogo ucheniia N.E.
Vvedenakogo dlia nevropatclogil. Moskva, Medgiz, 1953. 91 P.
(MIRA 16:7)
1, Chlen-korrespondent AMN SSSR (for Vasillyev).
(VVEDENSKII, NIKOLAI EVGENIEVICH, 1852-1922)
(NERVOUS SYSTEM--DISEASES) (PHYSIOLOGY)

OBROSOV, A.N.Y otv. red.; MUMINOV, Ya.K., zam. otv. red.; BULATOV,
P.K., red.;-VASIL'YEV, I." red.; DALIMOV, Z.A.p red.;
KATSENOVICH, R.A., red.; KETKO, M.I., red.; VINKH, A.A.,
red.; CHERNYAVSKIY, Ye.A., prof., red.; SHRAMKOVA, G.A., red.;
TSAY, A.A., tekhn. red.
(Aeroionization and hydroaeroionization in medicine] Aeroioni-
zatsitp. i'gidroaeroionizatsiia v meditsine; materialy. Red.
kollegiia: A.N.Obrosov i dr. Tashkent, Medgiz, 1962. 305 P.
(MIRA 16:6)
1. Vsesoyuznaya konferentsiya po aero- 1-gidroaeroionizataii,
Tashkent, 1960. 2. TSentrallnyy institut kurortologii i fizioterapii,
Moskva (for Obrosov). 3. Kafedra fiziologii cheloveka i zhivotnykh
Laningradskogo gosudarstvennogo universiteta (for Vasillyov). 4. Uz-
bekskly gosudarstvannyy nauchno-issladovatellskiy institut kurortolo-
gii i fizioterapili im.N.A.Semashko (for Katsenovich). 5. Gospit4q'-
naya terapevticheskaya klinika Leningradskogo gosudarstvemnogo me-
ditsinskogo instituta im. I.P.Pavlova (for Bulatov).
(AIR, IONIZED--THERAFEUTIG USE)

S- - L-f KOV, A. V.; VAQjL1-j-U1,-L. T . ; C~. A --'T L-rv~ r A. rG .
)
"A method for simultaneous determiration of all thermal properties of bai hr-at
conductors over the temperature range 800 to 5CO--~K."
report submitted but riot accepted for 3rd Symp on Thermophysical Properties,
Lafayette, Ind, 22-26 Mar 65.
Heat & Mass Transfer Inst, AS BSSR, Minsk.

V!t T L
wid I'nr
rF
-rpc.
no,6~!20- 2f-,,
T% -I PN

ACCESSION VR:- AP4038001 5/0110/64/000/003/0076/0084
AUTHORs Vasillyev, L. L. i
TITIZ: Method and apparatus for determining the thermal properties of heat
insulators in the temperature range of 80-5000K
SOURCEi Inzhonarno-flzichoskiy zhurnal, no. 5. 1964, 76-84 1
TOPIC TAGSt heat insulator, t1formal conductivity moasuroment, thermal difi)lsivity:
wasuremont, specific heat capacity, cryostat, fused quartz
A13STRACT: The authors attornin-fod to firyl the most convenient method of dotemining.
the coofficiojits of thermal conductivity, thormal ddfrusivity, and the specific
heat capacity of thermal insulators. The theory of such a method of dotermLining
t s :1B o ed
%,b9 thorvial properties of poor heat conductors at low toriporature pros nt .
The desigi and oporation of a cr-jostat used in the experiments is given. Invosti-
gations of the temperature dependence of the thoniial properties of fused quartz
were carrid out at 80-4000K as an illustration of the elaborated method. It was
found t1vi.-L fuaod quartz, can bo unod aa it atandard material In tostinGr now
methods and equipment employ3d In the determination of thermal proportion of
Card 1/2

ACCESSION 1IRt AP/4038001
materials, The combined use of the stationary and quasi-stationary methods
of determining thermal properties in the course of a singlo experiment provides
a means for the mutual chocking of experimental data. Orig. art. hast 4 fieuron,
13 formulas, and 1 table.
ASSOCIATICK: Irwtitut toplo-i maasootmona,, -AN BSSRp Miwk (Institute of Heat
and Hass Transfer,, AN BSSR)
SURnTTED: 18Dec63 DATE ACQ: OgJun64 ENCL t 00
SUB CODE: TD NO MW SM 003 oTms oo4.
Crd 2/2

VASILIYEV, L.L.
International Conference on Heat Transfer. Inzh.-fiz.zhur.
5 no.8:140-]J+I+ Ag 162. (~IIRA 15:11)
(Heat-Transmission--Congresses)

VASIL'Y-r,Vl 1.111.
Methoda and equipment for determ-frilng thax-z-1 properties of
heat-insulating matc-rJals in the temperature range from 80
to 5000 K. ln7b.,-f.Z. zhar. 7 no.5;76-84 14Y 164.
(M-17',RA 17.6)
t-.
1. InSt4tat teplCP_ i massoobmena ;-N R-,SR, I/Ilrisk.

-VASMI" L.L.
Precision amplifiers for thermal control in the range of
low temperatures. Inzh.-fiz. zhur. 6 no.9:105-110 S t63.
(MIRA 16:8)
1. Institut teplc- J. massoobmena AN BSSR, Minsk.

VISFINEVSKIY, B.P.; ~ASILIYEV, L.M.
Results of industrial introduction of complax equipment for
moistening coal in a mannif. Biiil.tokh.-ekon.inform.Gos.naucYi.-
Issl.inst.nauch.i, tekh.inform. no.9:14-17 163. (MIRA 16.10)

BRAGIN, B.K.; VASILIYEV, L.M.~ ZAFEVALOV, N.A.
Inw inertia tuh.-I-9--r fw-mce f,,- tes-tirg,
thermocoupleB. Izm. tekh. no.12zl9-20 D 161-
(MIRA 18-14)

__ (rji~;~ ) - I . .
VU)MIYEll, L.11., cand recn ';ci
he draiAng Of J.ands irl
t
~O
cc,.~ies (Y.L, 27-~B, 10'

W
VAS U i, I ~S-- - -
Sucivnsion mirr,)r level. good. I Imrt. no~5:75 Je '57. (YlRi 1':0)
(Curvoying-Instrumonts)

AUTHOR: Va ~qil I yev, L qraduate Stulent
TI'-PLE: Determining the Parameters of Correction Curves for Intro
ducing Decentrations Automatically (opredeleniye parar.Arov
korrelctsionnykh krivykh dlya avtomatichookojo vvedeniya
detsentratsiy)
PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy. Geol,~-,-Jya -;, -ierr-
fotoollyemka, 1958. Nr 1, P--.) 101-106 (USSR)
ABSTRACT: In locating air photographs by means of transformed i-,encils
of projectinr- lines, the inclinations by the aneles a and G)
of the cameras necesaitate the introduction of decentratiors,
forMUlae (1) and (2). Por an automatic displa.,zemer,-G of, t*,,.e
air photographs by the quantities A x and A y, Profts2nr
F., V. Drobyshev suggested a device utilizint,1- a correction
curve, which is shown here. - The formulae (8) are derived.
These formulae indicate that a section of the curve in the
range - a 4 a determined by the formula (4) ran be replaced
by another circle of the radius R 0, as the parameter cf th-js
circle does not depend on the current coordinate a. it 15
shown that for the processing of the air photoirraphs ob,~ainerl
Card 1/2 with cameras of different focal lengths a set of correction

SOV/ ! 1 54 - "f3 -
Determining the Parameters of Correction Cvrves for Introdi-in.-
Au t omat ical 1y
curves is necessary. The admissible deviation r of ho 17o c a
length of the projectinG camera fron the calculated value
F can be computed according to the formula ('11). Some in-
accuracies of this system are explained. Pinally a formula
for the decentration error is derived. It is '~-ointed cut
that an analogous error ir the scale inversor of the photc,
reductor of Profesnor F. V. Drobyahev occurs in a sect--on
with a small radius of curvature of the Prerch curve in an
enlargement of 0,6 to 0,8. There are 4 fiCiires and 2 talblos.
ASSOCIATION: Moskovskiy institut
kartografii
(Yoscow 11nil,ineerin.-.1
and CartogTaphy)
inzhenerov jeodezii, aerofotos"yerl.-_
Institute of Geodesy, Aerophcto~~raphy
Card 2/2

A A
Sol-Whass.. T. a.. Candidate at TOCK14401 set* ... 0
TITLIt Soleslifle and Technical Co.f.rocau, of NIICA i X (141.12AO-
kIsslabeekayg kastsr.stalym, N11rA 1 X) I
PIRIOVIC41. :34vastija wye.hikh uch.baykb saveddaly. 0.04.31js I
fOtgs*ye.". 1958. Ir 2. pp 111-114 (USSX)
:Z"
April 24 to 26 a scientific, &a4 technical conference or
LASTRACT.
tha1111aA I % (Institute of Geadvay, Aeraphatogrophy. med
Cartography, Moscou) was held In Moscow. Furtherwor*. there
war. four emotions to operations on gmedvoy. sarophot ageodesy.
41orlograptZ, and on the praduatiou of phatogrametrIcsl Inetr-
so to. More than )00 delegates from 45 lastitut*s took part in
tb: conference at which 28 lootarem, war& #Ivan. 20 4dlatl%te.
part Istpatod in to* dl.cusai.am. Th* opening speech ..* 0.6. by
Me DLr"%or of the XTICA I K. Professor P. S. 2*katov. tootor
Of Technical Salome- Th. first paper by 1:
ran +
Ivana, as -The fight 4641"t Do v r.
-TTWear. Doctor of Technical Salome-. spoke no "fro S-t,~p and
%be Levelling Principles, of the Ceadatic Beat. X.t..rk of the
Card 1/3 OSSR.* A. V. Drovets. Professor. read a paper on nTho ;.labor-
time %r. AIML.s to S,aa. lind. of G-04.klo.l
get a the Data Directly deamuired Lek tko
111,111plaid .- S. S. lWrav-y.v. Doomat. -On a Banco Mark or
Speoial StabllitY-o T, G. 3611khavowich. Docent. Candidate of
"Ohe a ~Tbw Lira and S41mattitle Itark, of A. P.
3VOT 5"011-shm, t .tual x
'10 -09r moso,remout. of Distant..
Meter Promise comiltiona.. N. 1. Y.Ya'l-, Assistant. -00 the
Methodology Of Nigh-Prool.ion Gonsomeetry In Firet.Cluse Tri.
oasgulatiche X.o 1. To. Sabirs -On %he Problem of DotornialnS
3"0 lUmteento of tuser%rientatLoo of Bid-Angle and 3jper-
lids AA#I* Aerial Caemrao.~ A. 11. F~mvxmv, Graduate Student.
On a Level Device With & rr..Ijr S..p.ad.d Reflector.' X. S.
Visilviyev reported on "Goodemy &94 Cartography at the gotta.
&I"of she govt.% Ye. ?I ArzMOOv On 'An Inve.tteetion
of the V114 Iftoothind Device With Sipportlad Rollers." L. _
*operator With Xlo;trlosl
;.ar`,"Tt:.3t "at. "mrs.
K~Lkhwytqv. baceet. r1andicate of Tathatati
Sol"coss -On the Chaell. or Scale of Aeritl Photographs It... It.
,OR ?roe galsrgemont.- P. T. Zkh,,ra,, "0. the D&.tIA.tIv.
c-pabiliti.. or blact-and-Whits, &n& Color 7hotograph-." Im. 1,
_KxssL.Qv, Ordoato St.d.mi. -Zoo j.1--to 4f be Theory f .
5- Nigh-Sysed, $bull"." 1. a. Spritla, Professors "Th* Present
State of jamelod4o on the Front.. P.m..
1$.a tag of measuring Tool.." 3. M. -Speeding 4p %.4
Z";Oviod the Prod"Slas of MostarI4 Toolm.~ L. A. Welkin,
scholcal Salome... -0. Instruso;t. for
PT" is;ix"sr~at at Dislancess.- 1. S. VoLh.yoftsv. Am-
,W: 11 -.1,
a. tea Tests with the Opttaal Use. Finder C1111.1.1
,. a. asoV. Assistant. '00 the Study of Inecomractoo in the
reau;sime Levine* of Telescopes.* X. N. jolkov. Professor.
D"S;r or Gtogrephlaal sciences$ ~3006 Avater,44 an Eadrawtne 10
the rodation, Process of Origival, Up.."
cart 3/)

..,JTHOR
TITLE:
PERIODICAL:
ABSTRACT:
None Given
sov/ 6-58-6-21/21
Card 1/3
Chronicle (Khronika)
Geodeziya i kartografiyaq 1958, Nr 6', PP- 79-80 (USSR)
From April 24 - 26, 1958 a Technical Scientific Conference
took place at the Moscow Institute of Surveying-, Aerial
Photography- and Cartography Engineers (Moskovskiy institut
inzhenerov geodezii, aerofotos"yemki i kartografii).
In the section of aarial-surveying the following lectures
were held: N. Ya. Bobir, Docent,- "On the Problem of the
Determination of Elements of the Internal Orientation of
Aerial Cameras With Wide and Superwide Angles". Ye. P.- Arzhanov,
Assistant, - "Investigation of the Apparatus for the-Straight-
ening of the Film by Means of Waves". (Compressed Airomechan-
ical Method by Docent A. I. Shershen'). V. Ya. Mikhaylovq
Docentp - "On the Change of the Scale of Aerial Photographs
in the Course of Enlarging". L. N. Vasillyev, Aspirant, -
ItStereocompensator With Eleot~i_c_T_orreotfo_~W~_. P. V. Zakharov,
Teacher, - "On the Fineness of Grain of Black and Vrnite as
Well as Color Negatives of Aerial Photographs". Yu. M.

Chronicle SOV/ 6-58-6-21/21
Kuznetsov, Aspirant, - "Elements of the Theory of the New
Rapid 3hutter".
In the section for surveying and photogrammetric apparatus
the following lectures were held: I. G. Sarkin, Professor,
"Physical and Mathematical Theaea of the Theorem on the Ac-
curacy of the Apparatus as a Means of Measurements". S. M.
Goloving Docent, -4Accelerating the Production Preparations
of New Pgaducts and Reducing Their Costs". L. A. Malkin,
Docent, -I'AnDaratus for the Exact Recording of Distances".
V. S. KUeyeehev.~, Assistant, -$Field Tests With the Light
Range Finder CBB-11' (In Moscow in August 1957). V. S- Usov,
Assistant, - "On the Investigation of the Errors of the
Focusing Devices of Telescopes".
In the section of cartography the following lectures werq'
held: N. M. Volkov, Professor, - "On the Engraving in the
Production of the Original Publicat~on Editions". A. V.
Naumov, Docent, - "Some Problems of t~e Household of Carto-
graphic Production". G. A. Ginzburg, Docent, - "On the Inter-
relation of the Distortions in Cartographic Projections".
L. A. Bogomolov, Docent, - "The Topographic E*ialuation of
Card 2,13 Aerial Photographs Taken From Airplanes and Helicopters in

'.hronicle
SOVI 6-58-6-21/21
the Cartographing of Areas Difficylt Of Access". A. S.
Tolstoukhov, Assistant, - "On the Representation of Reliefs
of Plane Areas on Topographic Maps".
1. Cartography 2. Aerial photography 3. Scientific reports
Card 3/3

3(4)
AUTHOR: Vasil lye 1*.~. . ~juaior Research Assistant 3011/154-58-5- 15/16
TITLE: A Stereocomparator With Electromechanical Correction
(Stercokonparator a clektroiiiekhanirbookoy korrektuiyey)
PERIODICAL: Izvestiya vysshikh uchebnykh zavedeniy. Geadeziya i aero-
fotoswyemka, 1958, Nr 5, PP 153 - 171 (USSR)
ABSTRACT: T1,1s in a presentation of considerations concerning a
further development of different variants of photo-
gram.metz-1c, space intersecting. The principle su--ested in
this paiur is based upon the use of a stereocoiriparator
which permits differential motions of the film holders
parallel to the principal axes of the device. These
supports are moved by electrical motors of a servo-system.,
aliich are connected with an electrical computer. This
Computer takes into account the running point coordinates,
and continually calculates the corrections during trans-
for-,ations and transforms them to mechanical displace~7,ents
of the servo-system. Soviet scientists have worked out
a method for determining, the relation between the coordi-
Card 1,13 nates obtained from tilted and horizontal photographs

A Stereocomparator With Electromechanical Correction S0111154-58-5-15118
through corrections to the cardinal focal length, which
considerably simplifies the structure of the formulae
(no transcendent functions). If nuch a new type of
corrective device in used, the photographs can be trans-
formed to a case of normal exposure. The transformed values
of the coordinates obtained with thin device are then
used in the computation of points of the terrain according
to very simple formulae. Such a type of equipment serves
for the determination of a limited number of points.
This paper describes the particular features of the theory
of the interpretation of photographs in a rectangular
frame of reference, this theory being taken account of in
the development of the principal lay-out of this device.
An the method presented of space intersecting is based
upon the work of Professor F. V. Drobyshev and Professor
G. V. Romanovskiy a presentation of the basic lines of
t)- theory for this instrument due to these authors is
included in this paper. No analysis of the method of space
Card 2/3 phototriangulation is given, but only the principal
procedure for obtaining the space coordinates of points

A Stereocomparator With Electromechanical Correction SOV/1~4-58-5-15/18
on the ground surface, which elucidates the operational
principle of the device.There are 13 figures, 2 tables
and 1 Soviet reference.
ASSOCIATION: Moskovskiy institut inzhenerov
karto.-rafii (Moscor, Institute
and Cartography Engineers)
SUBMITTED: March 10, 1958
geodezii, aerofotos"yemki i
of Geodesy, Aerial Surveying
Card 3/3

VASILIYEV, L. N.., Candidate Tech Sci (diss) -- "A stereocomparator system for
spatial phototriangulation using electric computers". Moscow, 1959. 20 pp
(Min Higher Edue USSR, Moscow Inst of Ebgineers of Geodesy, Aerial Photography
and Cartography), 150 copies (KL, No 24, 1959, 135)

VASILIYEV, L.N., karid, tekhn. nauk
SMG-4 Galileo-Santoni stereom!crcmeter. lzv. vys. ucheb. ,a-7.-,
geod. i aerof. nc.3:895-92 64. (M-~RA -lt5;3'j
1. Moskovskiy institut inzhenerov geodezii, aerofof4slyemki i
kartografii.

VASILIYEV, L.N.
.......
Calculating thp. tolerinces for the adjustment of card,%rj -In-k!.;
inphotogrowetric4n6truments. Geod. i kart. no.9:37-45 3 1614.
(MEV. 17: 12)

VASILIYEV, L.N., kand. tekhn. nauk
More exact theory of photogrametric intersection in otereogmphs.
Trudy MIGAIK no.50:53-56 162. (MA 16:7)
1. Kafedra fotogrammetrii Moskovskogo instituta inzhenerov
geodezii, aerofotos"yemki i kartografii.
J4

BPKHIN, A.S.; BORODZYUK, G.G.; LESHCHINSKIY, A.A.; OKSMAX9, A K.;
Yu.S:;
KOSMINSKIY, O.F.; MANUSHKIN, A.Ye.; MILEVSKIY,
DRIATSKIY, N.M.; VASILIYEV, V.V.; LIVDVICH, A.A.;
ORLEYEVSKIT' M.S.1 MOROZO I.A.; OKSIANj A.K.; EMI, G.S -
SOROKIN, M.F.; BUTLITSKIY', I.M.k VASI1,'YEV, L.N.[deceaB;4
GINTS., Yu.R.; VASILOYEV, ri.K.; LUGOVgK-QY,-r.Ye-., KIRILLOV,
Ye.V.; STRUYKINA, N.S.; I.BVINOV, X.G.;BLOKHIN, A.S., otv.
red.; GURIN, A.V., red.; SLUTSKIN, A.A., tekhn. red.
(K-1920-frequency telephone eyatem] SiBtema vyBokochasi~tnogo
telefonl.rovanila K-1920; informatsionnyi sborni)c~ (By)A.S.Blokhin
i dr. Moskva, Sviazlizdat, 1962. 319 p. (MIRA 16:4)
(Telephone)

AC C NRt A P1. GOI116618 80~ii&E- C''O.DE:-U R/O.020/6.6./167-/00.3/059.0-/01593
AUTHOR: Wkhavlov. B. M ; Bezmenov, A. Ya.; Vaf fflyev, L. S.
dRG: Institute of Organic Chemistry im. N, D. 7-alirskly. Academy of Sciences,.SSSR
(Institat orpnicheskoy khimil Akademii nauk SSSL,)
TITLE: The process of hydroboronating butadiene-1. 3A
SOURCE: AN SSSR. Doklady, v. 167, no. 3, 1966, 590493
TOPIC TAGS: butadiene, diborane, organic synthetic process, reaction mechanism
ABSTRACT: Elsewhere the present authors and V. G. Kiselev report the analysis of products
of a diborane reaction with butadiene-1, 3 (DAN, 155, 141 (1964). In the present paper the
authors synthesized 1-(hi clopentaneA(compound V) and 1-crotylboracyclopen-
. ~ne-3- ~1~
tane (compound VII) to clarify the structure of the I-aklenyl boracyclopentane fraction obtained
UDC; 542.91+647.244

ACC NR1 AP6011658
0
I
in that reaction. Both compounds were then hydroboronated with diborane. The experimental
procedure is detailed. The results indicate that fraction C8H15B is almost entirely in the form
of V11. This is attributed to the verified much faster rate of hydroboronation for V than V11.
Participation of the two compounds in the formation of isomeric butanediols during the oxida-
tion of product mix resulting from hydroboronation of butadiene-1, 3 was 78% for V and 22%
for VIL A schematic representation of the process of mono-hydroboronation, given in the
report, negates assumptions by H. C. Brown and associates that diborane Is capable of
attachment to butadiene-1,3 in the 1,4 position. The paper was presented by Academician
B. A. Kazans1dy 26 June 65.
SUB CODE: 07/ SUBM DATE: 21blay65/ ORIG REF: 002/ OTH REF: 003
2/2

4, X-r -1
101264-67-- EMITW/T I-P4 /'n W'WT,/RM
ACCM, AP6003492
AUTHOR: Gallchenko G. L.- Za
Bezmenov A Ya - I B. M.-
Mi-P-M--L0Y*--
ORG: ~bscow State University im. M. V. ~pmonosov
sitet); =Frltute ol UrGanic unemistry im. N. D. 2
(Institut organicheskoy khimii Akademij nauk 555H,
S;aEal2v S. M.; Va--illyev, L. S.;
Moskovskiy gosudarstvennyy univer-
linskiv. Academv of Sciences. SSSR
TITLE: Heat of formation of mothoxyboraoyelopentane and mathyl di-n-bu~ ~iric acid
SOURCE: AN SSSR. Doklady, v. 166, no. 1, 1966, 103105
4.--
TOPIC TAGS: heat of formation, boron compound, boric acid 4..,114
llr-n~
ABSTRACT; The heatof combustion%\,5aHC, of these compounds was determined calorimetricl
ally, using a p~e`cise wiTt-er calorimeter, and heats of formation were calculated sub-
sequently. Accuracy of determination was t~0.02%. The combustion products, CO and
H3B03P were determined gravimetrically or by base titration in the presence oi ma'nnitoil
respectively, Among the compounds investigated,, the (n-C HBOCH burned more com
pletely than the others. The.determined AH 0 298.150K wei,9)2
e '-91D t 0.6 kcal/Mole for;
liquid D B-OCH and -1590.9 :t 0.8 kcal/moie for liquid (n-G N) BOCH The A H of
c
polymerized 1::>TOCH3was also determined and was -9296.2 -k ai~~. 1hus, the calcul-
ated heat of polymerization was ^,-l kcal/mole. The polymer was prepared by keeping
the monomer in sealed ampules for 3 to 8 months at room temperature. It was a clear
Card 1/2 UDC: 541.1,11

T-12`4
ACC NR, AP6003492 20
viscous liquid with nD 1.4300. The calculated beats of fo=ation were -67,6 j-0.6
kcal/mole for liquid C> B--OGH3 and -131,9 1 0.8 kcal/=le for liquid (n-C,
ON)2BOCH3'
The calculated heat of cyclization of the C> B cycle was -1.6 t; 1.0 kcal/mZ
SUB CODEz 07/ SUBM DATES 05Apr65/ ORIG REFS 008/ OTH REFS 005
awm

L 18566-66 D1T(m)/WP(J)/T WINI&TDIRM
ACC NR: AP6002699 SOURCE CODEz UR/0062/65/000/012/2111/2120
AUTHORSt Bezmenovy A. Ya.1 Va Mi~_~Iov, B. H.
ORGZ Institute oil Organic ChemistEZ im. N. D. Zel-inakiy. Academy of Sciences.e
SSSR (Inws'itut organicheskoy khimii kkademii nauk SSSR)
TITLE: Organoboron compounds. Communication 15T, Hydroboration ofizoprene, cis-
and trans-pipar7lene
SOURCEI AN SSSR. lavestiyao Seriya khinicheskaya., no* 12, 1965p 21U-2120
A
t
iTOPIC TAGSt boronp boron compound,, organoyoron compounds isoprene, diene synthesis
ABSTRACT: The reaction of diborane ith isoprene and cis- and trans-piperylene was
investigated. The study is an ext'ision of previously published work of the zoi,
authors (Doklo AN SSSR (v pechati)). The experimental procedure followed here is
described by B. M. Mikhaylov, A. Ya. Bezmenov, L. S. Vasillyevp and V. G. Kiselev
(Dokl. AN SSSR 155, 141, 1964). A reaction mechanism is proposed, and the reaction
Yields and degree of monohydroboration are tabulated. The experimental results
are compared with literature values presented by G. Zweifel, K. Nagase,' and H. C.
Brown (J. Amer* Chem, Soc. 84, 183# 1962)o It was found that the degree of hydro--
Cardl/2
UDC t 5)a.91+0&.718.4

L 18566-66
ACC XR: AP(M2699
boration obtained was significantly higher thar~that obtained by Brown at al. The.
authors conclude that the addition of diboranO o dione-hydrocarborm occurs in tho
1,2 and 3,4 position; the addition in the 1j'4 position does not occur, Orig. art.
has: 3 tables and 20 equations.
SUB COM 07/ SUBM DAM 05Jul65/ ORTO IrWs 0051 OTH REN 005

MIKRAYLOV, B.M.; VA31LIYEV, L.S.- BEZVENOV, A.Ya.
Transformations of tetraethyl ester of butane-1,4-dithicboronic
acid under the effect till Izv. AN SSSR. Ser. khIM. no,4:
712-714 165. OMIRA 18:5.)
1. Institiit organicheskoy khimiL im. N.D.Zeliriskogo AN 333H.

UR (b Pr 5
A K04/z
- - -:
jw',~
J,
jv/. WW JW
CCtm6x-NP.'-. KPYO
AUTHOR* Mikhaylov, B. M. Vasil'yev, L. S.
TITLE: Boron organir compounds. "art 1141. Mutual transformations of bcron tria.1-1
kyls, borates, and eatet-, Qf -'-zv~un -,rv'1ni,( rv-31vzeil ',)y :ilk-Yidiborane.,
SOURCrN Zhurnal obshchey khimii, v. 35, no. 5, 1965, 925-929
TDPIC TAGS: boron organic compound, Ini:ane_, catalysis
L: I " 'Id
ABSTRAC Boron trialkyls reacting with estfirs of alkaneboronic acids tinder mi
conditions were used to prepare esters of dial)caneboronic acids. The reaction was
appllled to dimethyl esters of n-butane-, isopentane- and hexanebomnic dcil, and
als-D n-propanebororic acil--' J:-~ hoxvl ~n miyturp of ti-but,-n,~.boronic
dim--tl~yl es* !r and tri-Pz-hijt,111br)rine ir, presen,:f- oi
convertel to the ester of
tion:
2112D0111
R=n-C,,Kg
Card 1/4

L %f;Oc'
5-65
ACCESSION IIR: AP5013148
The me-chanism of the above r-eaction may be represented by the following series of
conversions, which regenemte the tetraalkyldiborane catalyst:
q0 0, QIn ng,
cat fl~H Op, H
+
Estpm of dialkaneboronic acids can also be synthesized from a boron trialkyl and
the ratio 2:1, as fo-Llaws'.

L 56505-65
ACCESSION NP- AP5013140
For reaction (2), the following series of conversions is possible:
RIBII A- R(OR13 f12BOR' + (F;'O),8ll
Olt,
+ it + R 11\
~Ofll
HIRH + RO(OR'), no/', + lylon'
\O Ir
H
+ + 113DI.-
NOR,
When dialkaneboronic acids are heated with or-thoborates, esters of alkaneboronic
acids are readily obtained-
9-11
RBBOR*+B(ORIS (4)
Orig. art. has; 4 equations.
ASSOCIATION,,, none
Card 3/4

L 56505-65
ACCESSIOll IIR: &PS013"48
SU13 CODE.- OC
ENCL.. 00
~SUBMITTED: 26Kar64
iqtl\- 4/4
Mill

AUTHORS: Mikhaylov~ B. M., and Va~iil'yev
r~
TITLE: Reaot--ons of dibc-rare and alky
and alkyl b,,-,ri:,, ac~ids and w,'h
PERIODICAL: Akademiya nauk SSSR. Doklady,
.4 A 0 2 /0' lo -
B ~03/B-120
L,, S
b;)rar.~-5 wth esters of 1~oriz
,h--l-analogs
v, '39, no. 'e.
TEXT: B. M. Mikhaylov (.'n sooperati-r. N.ith V A. Dorcirh-ov, R-2f,, DAN
130. 782, (1960)) nontiri,:ed -,he on d-.onrane and -.ha-. ilbcrane
forms with dialkylic osters. besldes the dib)rar.~-s. alkyll
boric. esters in r-s*~ers. yla-'CB:
8R. BORI - B H ---:) 12B 10R,), `R,BH'~,
2 6 e
auThors, (") haa h-,~ Lr h a r. L r~ -st -he
tion. The hydrogen 4F, ar. ard.
thus, al?yl--alkcx-,, bcrare an,~ a - fri 7.,.'
H
R2 BOR? t- BH 5 -4 RB'N ORI t R B 11.7, F lhn -.,re r -A i s c:-:~ r~, r.-,
boric eater and alkyl b~,rar~e; ?RB R-0i "nR- R-Oil-
Card 1/6 c'R

Vo:- 0 A 5 ~-' A)o ~2
Reactions cf dibo~an~' and; al'-'
(3) are only d-~agrammat-- ~-al rtprezr-rta--, --s-IC-3 ~.n
they proceedwilh n of und
(see diagram)., Alky! B H -3
part w4th dialkyl lb;:-,:~ ir; ii J,
atom: R BORI - RBH- ---~ FB R-PH .1 I'n :s i al kv:
2 1OR.
box-ane dimerizing -r-- 1-b-:-tzle ar'-i i r
is converted according ~z :--4 2-,4
direcotion of the pr-lmary Or. e a I kI dialky!
ester is replaced by a hydrogen a-m, In t
dialkyl borane and alkoxy hor-.re: R-POR; - BH R-GBH-,
Moreover, the au"nora -.hlrik thtt
R BORI + RIOBH 2RB 6'~ a :-[I R O-ai'mi, ana
2 2 0a, .'R
R I OBH 1 /3 R0) B -1
2 BH' 8! In 5 a I kx f br an -i a r
decomposed tc ortY-oboratqs and to diborane a
dialkoxy borane). A c, tua 11 y t h -1 a -, es - ou I d bt. ~i - r. d -~ n s ~T. al 1 ar,!j -,i r, t a
Card 2/ 6

2 5 'Y
S/020/61/1,39/002/0112/01-1
Reactions of diborane and alkyl B103IB22n,
by fractionating the rea--tion produo:ts. Consequently, also *his int.al
direction of reaction results in the formation of -.he same final products
according to (5) as well as to (3? and (4). Orthoborates react with tetra-
alkyl diboranes. Ascording to (9) alkyl boric eaters are formed slowly at
room temperature and rapidly at 60-1000C with a yield of abol.3t, 80%:
(R 2BH)2 + 2(RIO) 3 B ---P 3RB (OR 2 ) 2 + (RBH 2)2 (9). In this case, the initial
stage is based on the substitution of a hydrogen atom in tetraalkyl borane
for an aikoxyl group: R2BH t (RIO) 3B -1 R 2BOR' f (RIO) 2BH ('0). The
further conversions of the dialkyl boric eaters and dialkyl diboranea (',0)
are analogous to those in (6)-(8) and an alky, b,,)r--,~ and an
alkyl borane being formed.' The reactions are reversib!-~- This is
proved by; 3 (R BH) BOR; . BI~H where
2 2 , 4RBIOR,)2 ~-~ SR 2 - 6
R - n-CXH 7 ; RI - C113 . Also the conversion of dialky! diborare !,- d;b.-.,rane
B H `12'-
and tetraalkyl diborane is reversible; 2R,B H R B H, 6
2 4
For this reason, the reaction proc-eeds cn boiling of tetraalkyl A-b~rane with
orthoborate not according to (9) but -o:
Card 3/6

25782
S/020/61,/139/002/0- 2/01, 7
Reactions of dibcrane and alkyl B-,O3/B22O
3 (R2BH)2 + 8 (Rfo) 3B --4 :2RB (OR?)P + B2H 6 ( 1 ")) .. Thu a ~ I OV1* d I b -) ran e
referred to (13) were isolated after 2 hr of b:-~-Jl;ng tetza-n-proj,yl
diborane and methyl borate. On dist-11lation of the reaction produ:,;s, 801%
of n-propyl boric dimethyl ester -Ais obtained. Moreover, it wa3 3-.a'~ed that
dialkyl di4boranes form *etraalkyl diboranes, with lr,~:-cn trtaiky2s. Th~
tetraalkyl d1boranes were used In catalytic quant;.ties 'in the rea-Iti,ins
between boron trialkyl3. orthoborates and alkyl bcri'~ eaters (1,14),
and (16)(see prell-minary 'Dmirunir~aticn of the authors (Ref. 6-. 1 z AN.
SSSR, OW, 196,,,, No. 3, 5311, At about 200" C.. eaters either of a-'k-y! or
of dialkyl boric acids are formed dependent on the cha-aoter of -,he alkyl
group in the boron trialkyl. High yields of theestere mentioned 7(D.-
are obtained even at 60-IOOOC by using the catalyst mentioned kor dib,?:-ane,
its alkyl, alk ~nd alkyl mercapto derivatives):
~RY6 ;P
R3B + 2 (RIO) 2 -~ 3RB (ORI)2 (14). (14) finally takes the fcrm of
(9) so that tetraalkyl diborane catalyzes the process and is regenerated
continuously. Likewise, esters of dialkyl boric acids are converted to
those of alkyl boric acids with a yield of 70-90'/'o;
Card 4/6

782
002 0/6,1 /L' 1 7
S 1'39100210'-
,
Reactions of diborane and alkyl B';03/B220
(R 2BH)
4 2RB (OR')2 (15), Also in rhis case . firs- of all
R2BORI + (R?0)3 B
dialkyloxy borane is formed which converts the dialkyl boric esters te~
alkyl boric esters either directly (in analogy to (6) ard (3)) or passing
the stage of decomposition into diborane and orthobarate (.-,n anaIogy to (8)
and (1)). Thereby, tetraalkyl diborane is regenerated. Finally, a reverse
conversion of the esters is possible: dialkyl boric a3idean be -formed from
an equimolar mixture boron tria:kyl - alkyl boric eater by the above-
mentioned catalysis:
~R2 BH')2
BORI (16). The yield in esters amo-.-nts to
B + RB 2R
R
,
2
I/
50-70%. (10, (15), and (16) are simple in preparati-,e respec.4; and ther~--
are not known any other rea-tions giving the same resjit'.. The rht-D-analogs
of the orthoborates and the ;-sters of the arc~ida mentiored bi~have similarly.-
(R2BH)9
2 (RS) 3B + R3B 3RB (SR~ where R ~ n-.C 4H9 A s m aI I -.- -,-i --) u r, t : f
n-butyl th.-oboric-r-butyl ester was jaclated as by-prodlll-i~, Th,.3 reaction
requires more severe ';ondit.ioni than that with c~rthob-,~--ates-. T~~traalkyi
Card 5/6

25782
S'/020/61/' 7
Reactions of diborane and alkyl B-03/B220
mercapto-diborane is a more stable --,)mpQund !,hari dialkoly ~,:)rare~ wni
(in analogy to (8)) de,:omposes eas;.y to d-_borane and l1 t
a ~ t rsra r -a s
concluded from this f-t---t that, no-, dialkoxy bor ne t dil n, 4
those reactions whqre 4.lalkoxy borantia ar,y ,,nvolv~?d and oxchazlgo
hydrogen atom against the alky! group at low
7 references; 4 Soviet- bloc and 3 n -blo T"-.-- ref~:~n,_-es -0
English-language publi~;ations read as Afollows: A, P., Bi;rg, H~
Schlesinger (Ref. 2. J. Am. Chem. So;:.., 4020 ('93i
Thomas (Ref. 4: Am pat. '4635693 (19;8)). )
ASSOCIATION: Institut organioheskoy kh,,mii im~~ N. D Z~l:.r5kQg_-: Akaziemli
nauk SSSR (Instilute of Organic Chem_,6try .merli N. D.
ZA_1Jnski,y of the Academy of Solen_-es USSRI
PRESENTED: March 28, 1961 by B., A, Kazanskiy, Academician
SUBMITTED: March 22, 1961
Card 6/6

MIKRAYLOV, B.M.; VASILIYEEV, -L.S.
New methods for synthesizing esters of alkyl borouic acids. Izv.AB
SSSR otd.khim.nauk no&3t531-532 Mr 161. (MIU 14:4)
". Institut organicheskoy khimii imeni N.D.Zelinakogo AN SSSR.
(Boronic acid)

B1214ENOV, A.Ya.; VASIL'YF.V, L.S.; MIKHAYLOV, B.M.
Organoboron ccupounds. R"rt No.157s Hydroboration of
iaoprone, cis- and trano-piperylane. Izv.AN SSSR.Ser.khim.
no.12:23-11-2120 165. (MIRA 18: 12)
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.
Submitted JulY 5, 1965d

MIKHAYI-OV,, B.M.; AKHNAZAFffANp A.A*;-.VASIUIYEV,, L.8.
.Sjmtheals and properties of tetrA~-Propyldlborane and tetm-n-
butyldiborane. DAL AN SSSR 136 no.4%828-831 F 161.
1 1 (MIRA .14:1)
1. lwtitut organiebodkoy khWi imeni N.D, Zelinatkogo AkademU
nauk SSSR. Predstavleno akademikom B.A. Kanaskim. I
(Diborane)

209)45
S/062/6 2) /^_1
T) 0 B117/B20,6
AUTHORS: Mikhaylov, B, M. and Vasil~yev, L. 3-
TITLE% New method of synthesizing alkyl boric acid esters
PERIODICAL: Izvestiya Akademii nauk SSSR. Otdelenlye khimicheskikh
nauk, no. 3, 1961, 531-532
TEXT: In this "Letter to the Editor", the authors report that they have
found a new method of synthesizing alkyl boric acid esters while studying
the properties of tetraalkyl diboranes obtained previously (Ref. 1;
B. M. Mikhaylov, A. A. Akhnazaryan, L. S, Vasillyev, Dokl. AN SSSR 156,
828, 1961). Tetraalkyl diboranes were found to react with orthoborates
slowly at room temperature and quickly when heated (800-10000), giving
alkyl boric acid esters (80-90 % yield
R B H + 2(R'0) B - 3RB(OR'~- 1/2 R B H
4 2 2 3 2 2 2 4
R - n-C 3H, n - C 4H9; R'= CH 39 n-C3H 71n C7H15'
Reaction 1.) proceeds via several stages, alkyl and alkoxyl groups being
subgtituted for the hydrogen in tetraalkyl boranes and their primary
Card 1/2

209a5
S/062/61/0-~0/003/012/0';~
New method of synthesizing alkyl... B117/B208
conversion products. It was further found that dialkyl diboranes react
with trialkyl borines (particularly readily when heated) to give tetra-
alkyl diboranes: R 2B2H4 + 2R 3B 2R 4B H The possibility of con-artIng
dialkyl diboranes resulting from reactio Into tetraalkyl diboranes in
n
the presence of trialkyl borines permitted the synthesis of alky! boric
acid esters from trialkyl borines and ortho-borates under the action of
catalytic amounts of tetraalkyl diboranes.. In this way, various alkyl
boric acid esters were obtained by heating the above components up to
800-1000C (80-90 % yield) R 3B + 2(R'r)) 3BR5B2H2 3RB(OR'N.. iAbstracter-s
note: This is a full translation from the original.., There is 1 Soviet-
bloc reference.
ASSOCIATION: Institut organicheskoy khimii im. N. D, Zelinskogo Akademli
nauk SSSR (Institute of Organic Chemistry Imeni N. D. Zelinskiy.
Academy of Sciences USSR)
SUBMITTED: January 16, 1961
Card 2/2

88406
B/020/61/136/004/014/026
B016/BO75
AUTHORSa Mikhaylov, B. X., Akhnazaryan, A. A., and Vasillyev, L. S.
TITLEs Synthesig and Proportion of Totra-n-propyl Diborane and
Tetra-n-butyl Diborane
PERIODICAL3 Doklady Akademii nauk SSSR, 1961j Vol. 1)6, No- 4,
pp. 828 - 831
TEM The authors studied the reaction of diborane with tri-n-propyl boron
and tri-n-butyl boron in otheric solution, and determined the following
factes 1) When passing 1 mole of diborane through a 4-mole solution of
boron trialkyl at room temperature, tetraalkyl diboranes are produced in
a yield of 70-85%, i.e., tetra-n-propyl or tetra-n-butyl diborEne. 2) When
using an equimolecular quantity of diborans, an asyametric di-n-propyl
diborane is isolated by distilling the reaction products. The second
synthesis method is based on the reaction between diborane and olefins
(Ref-4). This reaction is catalyzed by different others. Reaction 8f
diborane with propylene-1 and butene-1 (ratio 1 A 4) at -70 to -30 C in an
etheric medium resulted in a 46% yield of tetraalkyl diboranes. The latter
Card 1/3

88406
Synthesis and Properties of Tetr&-n-propyl 8/020/61/136/004/014/026
Diborane and Tetra-n-butyl Diborane B016/BO75
are completely stable up to 100 0C and can be distilled in vacuo. In
benzene solution they are partly dissociated into dialkyl borane. Tetra-
alkyl diboranes spontaneously inflame in the open air. They are highly
reactive and react with alcohols under the formation of dialkyl borio acid
esters. With aniline they form dialkyl phonyl amino boron. Under the
action of mercaptans, tetraalkyl diboranes are converted to dialkylthio-
boric acid. Such reactions are convenient preparation methods for
synthesizing organoboron compounds, since only small quantities of side-
products are formed. Tetra-n-butyl diboranes more difficultly react with
glycol. In this came, almost equal quantities of glycol esters of di-n-
butyl boron and n-butyl boric acid are formed, and, in addition, tri-n-
butyl boron. From the formation of the latter, the following was con-
oludeds The action of nuoleophilic reagents causes a substitution of
hydrogen atoms by tetraalkyl diboranes, and also a disproportionstion of
tetraalkyl diboranes into boron trialkyls and alkyl boranes. Under the
action of a nucleophilic reagent, the alkyl borans thus forming results in
an organoborot compound with a radical on the boron atom. On the other
hand, boron trialkyl remains either unchanged (e.g., in the rtaotion with
glycol), or enters into reaction and, e.g., with marcaptan, forms an
Card 2/3

88406
Synthesis and Proportion of Tetra-n-propyl S/020J61/136/004/014/026
Diborane and Tetra-n-butyl Diborane B016/BO75
ester of dialkyl thioborio acid (Ref.6). In the latter came, hydrogen an
well an a or-".l quantity of propane are present in the gaseous reaction
products. A metric boron trialkyle can be synthesized by reacting totra-
alkyl diborLaos with olefins. There are 12 reforenomai 6 Soviet and 4 US.
ASSOCIATIONs Institut organicheskoy khinii im. N. D. Zelinskogo kkadenii
nauk SSSR (Institute of Organic Chemistry imeni
N. D. Z*linakiy, Academy of Sciences USSR)
PRESENTED: July 9, 1960, by B. A. Kazanskiy, Academician
SUBMITTED: July 6, 196o
Card 3/3

MIRPAYLOV, B.M.; VASILIM, L.S.
Exchange reactions between boric organoboric acid ester5 and their
thio analogs. Izv.AN SSSR.Otd.khim.nauk no.11:2101-2102 n 61.
(MIRA 14:11)
1. Institut organicheskoy khimii in. N.D.Zelinskogo AN SSSR.
(Boric acid) (Boron compounds)

IIIEIAYLOV, B.1-1; Vi`,:~ILIYLV, L.S.
Orannoboron compounds. Report 11o.99: Reaction of
tetraalkylcUboraneD -with boric acid esters. Izv. AN S5,ZF. Ctd.
khim.nauk no.5:827-833 MY 162. (RIRA 15:6)
1. Institut organicheskoy khimii im. R.D.Zelinskogo Ali SSSR.
(Diborane) (Boric acid)

MIKHAYLOV, B.M.; VASIL' FEV, L.S..
Organoboron compounds. Report No.97: Action of diborane on
esters of dialkyl boric acids. Izv.AN SSSR Otd.khim.nauk
no.4:628-634 Ap '62. (MIRA 15W
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN SSSR.
(Boron hydrides) (Boric acid) -
4

VASIL'YEV, L. S.
"Genezis drevnekitayskoy bronzy 11, etnoiul'turiye In'."
report submitted for 7th Intl Cong, Anthropological ~c Ethnalog-11---al S----Iences,
Moscow, 3-10 Aug 64.

MIKHAYLOV, B.M.; VASIL'YEV, L.S.
ReactionB of dibarane and alk7ldibvranes with boric and aLkylboric
acid eaters and their thio analogs. Dokl. All S'S.':IR 139 no.2:385-388
J1 161. (MIRA 14:7)
1. Institut organicheskoy khimii im. N.D. Zelinskogo AN SSSF.
Predstavleno akademikom B.A. Ka7anskim,
(Liborane) (Boric acid) (Boron hydrides)

AUTHORS:
TITLE:
37101
S/062/62/G00/GG5/00-1/G3,-,
B110/B101
Mikhaylov, B. M., and Vasillyev, L. S.
Organoboron compounds. 99. Reaction of tetraalkyl diboranes
with boxic acid caters
PERIODICAL: Akademiya, nauk SSSR. Izvestiya. Otdeleniye khimicheskikh
nauk, no. 5, 19062, 827 - 833
T3XT: In continuation of previous papers by the authors (Izv. 1,11 ',,'-:!SR.
Otd. khim. n. 1961, 531; Dokl. AN SSSR 139, 385 (1961)), the conversion
of tetraalkyl diboranes with orthoboric acid esters into alkyl boric acid
estersis investigated. Trimethyl, tri-n-butyl, tri-n-heptyl, and tri-n-
heptyl borate with tetra-n-propyl diborane and tetra-n-butyl diborane were
used in different ratios and under different conditions. After 2-5 hrs in
the water bath tetra-n-propyl diborane and tri-n-heptyl borate (1:2) give
rise to the di-n-heptyl ester of n-propylic acid in a yield of 80 ~-,:
(-12BH)2+ 2(RIO) 3B --) 3RB (OR I )2+ (1/2)(RBH 2)2; R -n-C3H7; RI =n-07H15'
Some alkyl diborane or dialkoxy borane is also formed. In the initial
stade of the reaction between tetraalkyl diboranes and orthoborates,
Card 1/4

S106 02/G30/G0,:Z/,j,;,
101
Organoboron compounds. 99. B11OV,
hydrogen is exchanged for the alkoxy group to form the ester of dialkyl
boric acid and dialkoxy borane:
R R R H .-,OR,+
IN, + WOV - --~B'-
--'0'-- ~IOR'
W
R OR'
B R,BOR'+ MOW),
R 0 " --OR'
R' e - --
borane is then symmetrized to diborane and borate according- to:
3HB(OR.) "IC-2B(ORP) + (1/2)B H Diborane then converts dialkyl boric
2- 3 2 6'
a
c~
'd ester into alkyl boric acid ester and dialkyl diborane. Since
dialkoxy borane possesses a B-H bond, it can also react vii-~h the iritial
tetraalkyl diborane: (R BH) +2HB(MI) ---~'(R +211B(OV)2 or 7"th
2 2 2 Nz- BH2)2
KIt
dialk.11 boric acid ester:
Card 2/4

S1062V62100-100510031OC6
Dr&anoboron compounds. 99. B11O/BIOI
H
30' RB The resulting alkyl alkoxy borane
V + HBNR,)~~::? + RB(ORI)
R
2 OR' 2*
is able to symmetrize to the ester of alkyl boric acid and dialkyl dibo-
rane or it may exchange its hydrogen atom for the alkoxy group. The
following products viere synthesized: (1 n-heptyl ester of di-n-pro-jyl
oc
boric acid (b. p. 92 - 97 /4-5 mm Hg; nDo = 1.4250), (2) di-n-hepty'l
20
ester of n-propyl boric acid (b. p. 120 -1230C/3-5 mm Hg; nD = 1.429219
(3) tri-n-heptyl borate (b. p. 157 - 1600C/3-mm Hg; n20 =1.4315), (4)
D - 20
dimethyl ester of n-propyl boric acid (10- P- 58 -650C/107 mm He'. nD
1 65
0
1-3845), (5) di-n-butyl ester of n-propyl boric acid (b. p.
20
- -7(,,C)C/)=IT n=1-4112), (6) dimethyl ester of n-propyl boric acid (b. p.
, D 20
45 -560C/95 mm. EIg; nD 1.3853), (7) di-n-propyl-(phenyl amino)
20
(b. P. 76--81OC/2 mm, Hg nD - 1.5055), (8) dimethyl ester of n-butyl boric
acid (b.p- 51 - 540C/43 = Hg; n 20 . 1.3950), (9) di-n-butyl-bis-(phonyl
D
Card 3/4

S/062/062/000/005/003/008
Organoboron compounds. 99. B110/BlOl
20
amino)boron (b. p. 111 - 1140C/4 mm Hg; nD . 1.4960), (10) n-lbutyl-bis-
(phenyl amino)boron (b. p.' 128 - 1320C/0.06 mn Hg; n 20 = 1.5720).
D
ASSOCIATION; Inatitut organicheskoy khimii im. N. D. Zelinskop Alkadenii
nauk SSSR (Institute of Organic Chemiszry imeni N. D.
Zelinskiy of the Academy of Sciences USSR)
December 6, 1961
Card 4/4

-3219
S/020/62/147/007/on/o,-7
13101/13186
AUTHORS: Mikhaylov, B. M., Vasil'yev, L. S., Safonova, E. N.
TITLE: Conversion of cyclic boron compounds under the action of
methyl borate
PERIODICAL: Akademiya nauk SSSR. Doklady, v. 147, no. 3, 1962, 630 - 633
TEXT: The following reactions are described: (1) Di-1,4-0-boracyclopen-
tyl)-butane (I) and methyl borate (molar ratio 1:1) were boiled foE 1.5 bra
in the presence of tetra-n-propyl diborane, then kept at 130 - 135 C for
another 1.5 hrs, and fractionated; thereby 80.5% 1-metboxy-boracyclopentane
(II), biP. 40.5 - 41-OOC 63 min Hg, d 20 0.8421, n20 1.4172, was obtained as
4 D
well as the by-product 1.6-dimethoxy-1,6-diboracyclodecane (III), b.p.
69.5 - 70-0'C/2-5 mm fig, d 20 0.9055, n 20 1.4538. (2) Boiling of II with
4 D
methyl borate in the presence of tetra-n-propyl diborane yielded 71-50,"~
tetramethyl ester (IV) of butane-1,4-diboric acid, b.p. 5'4 - 56 OC/2-5 mmHg,
Card 1/3

S/020/62/147/003/024/027
Conversion of cyclic boron ... B101/B186
n 20 1.4175, and methyl ester (V) of di(4-dimethoxy boryl butyl)-boric acid,
D 20
b.p. 116 - 1200C/2 mm fig, n D 1.4360. The compounds IV and V were also
: 5. '3)
obtained by renction between I and methyl borate at a ratio 1 1,
Interesterification of IV and n-hexanol yielded 98.5%6 tetra-n-hexil ester
(VI) of butane-1,4-diboric acid, b.p. 198 - 200'C/1-5 mm Hg, d 20 0.8667,
20 4 0
VII) b.p . 44 - 45 C/aTM
n D 1.4402. W 72-4. 1-n-hexoxy-boracyclopentane (
Hg, d20 0 8386 n 20 1.4382, and tri-n-hexyl borate, b.p. 129 1550C/2-5 am
Hg, nso 1:4270'we'1r)e obtained by keeping VI for 1.5 hrs at 270 3000C. The
compounds !I and VII polymerized when left standing; but the polymer so
formed, decomposes again when heated. (5) The reaction of diborane with
diallyl dissolved in ether (ratio 1 : 4) yielded di-1,6-(l-boracycloheptyv-
hexane and 6-(l-boracycloheptyl)-hexene-1, b.P. 57 - 59 0C/3 mm fig,
d 20 0.8214, n 20 1.4630 in almost equimolecular ratios. (6) 81~a' 1-methoxy
4 D 20 20
boracyclopentane (X), b.p. 42 - 43OC/15 mm fig, d 4 o.864, n D 1.4591, was
Card 2/3

310201621147100310241027
Conversion of cyclic boron B101/B186
obtained by heating V111 and methane (ratio 1 : 1) in the prouence of
tetra-n-propyl diborane. The same reaction (ratio I : 5) yielded equi-
molar amounts of X and tetramethyl ester (XI) of hexane-1,6-diboric acid,
0 20 20 -
b.p. 82 - 84 C/1-5 MM If[,,,, d40.9325, nD 1.4252. XI wan also obtained
by reaction of X and methyl borate. The Engliah-language reference ist
K. Saegebarth, J. Am-. Chem. Soc., 82, 2082-(1960).
PRESENTEDs July 17, 1962, by B. A. Kazanskiy, Academician
SUBMITTED: July 12, 1962
Card 3/3

MIKHAYLQV, B.M.; VASILIM, L.S.
Organoboron compounds. Report Ko.110z Catalytic conversion of trj-
alkylboronic acid eaters under the effect of tetraalkyldiboranea.
Iav, AN SSWt.Otd,kh:Lm*nauk no,10:11564762 0 162* (KOU 15 tlO)
i
1. Institut organiche,ploy khimii im. N.D.ZelinBko 0 AN SSSR.
(Boron organic compounds

MIKBAYLOV, 13.14.; BEMNOV, A. Ya.;,. VASIL I YFV, L.S.; KISELFV, V.G.
Cyclic compounds of boron forrod during hydroborination of
1,3-butadiene. Dokl. AN SSSR 155 no.1:141-144 Mr 164.
(MIR' 17:4)
1. Institut organicheakoy khimii im. N.D.Zolinskoilo AN SSSR.
Predstavleno akademikom B.A.Kazanskim.

NINHAYIA)Vp B.M.; VASIL$YBV) L.B.; SAFONOVA,, E.N.
Tr9kneformatiOns of boron cyalic) compoundo umder the action Of
methyl boratee Dokle w MR 147 no.3s630433 3 162. (KERA 15:12)
1. predotavleno skadmikm B.A* Kazanskim-
(Dorm organic OOMPOunds) (Methyl borate)

BnYAKoV, F.Ye.; BABIN, B.N.; BALI, V.; BOROVKOV, P.N.; VOYYVODIR, I.N.;
G[JRXVICH, G.M.; GORBUNOVA, P.I.; KONNOV, A.S.; KALANTAROVA, M.V.;
KASHIRSKIY, A.Ya.; KAZAHCHEYEV, Ye.N.; LEKSTMKIN, A.F.; LRTI-
CHIVSKIY, M.A.; LOPATIH, S.Z.; MIRSKIY, Y.N.; PODSWALOV, V.H.;
SOBOTINA, V.P.; TAIIASIYCIIIX, N.P.; FEDOTOV, S.D.; FISEIWO, K.N.;
ELIKIND, I.G.; BOVIN, S.S.; VASILIYEV, L.T.; DRINKOV, V.D.; DALE-
CHIN, N.I.; DADAGOV, I.A.; I.V.; ZIMIN,
D.A.; IVANNIKOV, A.Ya.; KOVALXV. M.K.; LUGAKOVSKIY, H.L.; NALEVSKIY.
A.F.; SERE2MUKOV, V.K.; SEMIGLASIOV, M.D.; SOKOLOV, A.V.; SITPANOV,
V.I.; SAIULUUN, G.S.; SAVENKO, P.A.; SOLODOV, V.P.; UMBROV, Sh.Kh.;
CHIKINDAS, G.S.; SHCHMUKHINA, S.N.; DYIMIN, G.Z.; LYSOV, V.S.;
OSMOVICH, A.N.; ROKITSINSKIY, E.V.; MSLAVSKIY, H.S.; RUMTKC,
I.A.; ZUKOBORSKIY, M.S.; ZHDANOV, I.Ye.; SUSLIN, V.A.; BRUS, A.Ye.;
VOLYNSKIY, S.A.; KLYUUV, V.A.; ISTRATOV, A.G.; TIKHOMIROV, I.F.;
BUTYRIN, Ya.H.; VOLYNSKIY, S.A.; MINNYEV, M.F.; MALITSEV, V.I.;
VIDETSKIY, A.F., kand.tekhn.nauk, glavnyy red.; DEMIDOV, A.11., red.;
KRAVETS, A.L., red.; KLIMOVI, Z.I., teldm.red.
LIndustrial Astrakhan] Promyshlennnia Astrakhan'. Astrakhan',
Izd-vo gazety *Volga," 1959. 318 p. (MIRA 12:11)
1. Astrakhan (Province) Bkonorlicheskiy adniiiistrativnyy rayon,
(Astrakhan Province--Economic conditions)

MIKHAYLOV, B~M~, VASIL'YEVY L.S.
Y
Organobaron compounds. Part 141-.- 1+atual transformations of
trialkylborons, borates, and boronic acid esters catalyzed by
alkyldiboranes. Zhur. ob. khim. 35 no.5;925-929 My 165.
(MIRA 18:6)

MIKKAYLOV, BX; 1~~ILIYEVL_Lt&
Organoboron compounds. Part 1521 Mutual exchange of alkoxy-
and alkylmrcapto groups in drganoboron compounds. Zhur. ob.
khim. 35 no.6tlO73-1078 Je 165. (MIRA l8s6)

USSR /Engineering - Hydraulics, Dams Jun 51
"New Design of Multiple-Arch-Type Dam," L. V. Va-
s:Ll-'yev, Engr
"Gidrotekh Stroi" No 6, PP 38,39
Attempts to improve construction of multiple-arch
dms in respect to their sensitivity to unequal
settlement and temp influence. Suggests a new de-
sign which differs from existing structures as
follows: Each arch barrel consists of a series
of arches, placed upon each other and connected
mong them elves and to buttresses by watertight
LUSE/Engineering - Hydraulics, Dams Jun 51
(Contd)
jointo; each section has a tie-piece which accepts
tbr-ust; sep arch sections are prefabricated and
installed after erection of buttresses and service
bridge.