SCIENTIFIC ABSTRACT USOVA, YE.M. - USPANOV, U.U.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001858210007-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 7
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

L 28067-66
ACC NRs AP6015289
rinsing. All the factors which promote the increase of hydrogen content in the
surface layer improve the adhesion of copper plating to titanium. The potential of
activated titanium reaches a value of minus 0.78-0.8V In 2-3 sec and then remains
almost constant. -Orig. art. has: 4 figures. [WWI.
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USCIA, Yl~. V'.
USOVA, YE. Fl. -- "On the Formation of Benzene Hydroxanic Acids
and Some of Their Derlvativ,.-s." Min Higher &,uvati on Ukrainian SS-R,
Kharlkov Order of Labor Red Banner State University J--ieni A. M. Gor'kiy,
Kharlkov, 1956. (Dissertation for the Degree of Candidate of Chemical
r,
Sciences)
Letoni-s' No 43, October 1956, Mo--cow
SO: Knizhnay

USSR/Organic Chemistry. Theoretical and General E-1
Questions of Organic Chemistry.
Abs Jour Ref Zhur - Khimiya, No. 81 1957, 26675 D
Author Usova Ye M
Inst id~~o ~~ rsity.
Title To the Question of Structure of Benthydrox-
amic Acids and of) Some Derivatives of Theirs.
Orig Pub Avtoref. diss. kand. khim. n., KharIkovsk.
un-t, KharIkov, 1956,
Abstract No abstract.
Card 1/1

nENISOV, P.V. [Danysov, P.V.]; BUGAYEV, A.L. [Buhaiov, A.L.1; USOVA, Ye.M.
Chemical coaposition of snow [with summary, in ErglishJ. Dop. AN
URSR no.3:289-291 '58. OURA 11: 5 )
l.Kharkivalkiy zootekhnichniy institut. Predstavleno akademikom
AN USSR A.I. K!prianovym.
(Snow)

AUTHORt USOVA'Ye.M., VOROSHIN,Ye.M. 20-6-34/59
TiTLEr On the Structure of Hydroxamic Acids and some of their Derivatives
by means of Infrared Spectroscopy. (Isaledovaniye stroyaniya
gidroksamovykh kislot i nekotorykh ikh proizvodnykh metodom infra-
krasnoy spektroskopii, Russian)
PERIODICALa Doklady Akademii Nauk SSBR, 1957, Vol 113, Nr 6,.pp 1306-1309
N.S.S.R.)
ABSTRACTs The properties of benz-hydroxamic acids were closely investigated,
but hitherto, no sufficient explanation has been found for their
chemical structure. A double structure was ascribed to them;
either the oxygen atom is attached by a double binding to the first
carbon atom outside the benzenecycle, or it is attached to a
nitrogen atom in the hydroxyle. A still greater unclearness exists
concerning the aryl derivative of dibenzhydronamic acid - the
tribenz hydroxylamine which exists in two crystal modifications a
and 8 with different melting temperatures and solubility. According
to some authors they are physical polymorphs, others count them
among the tautomers, i.e. hydroxamic- and hydrozymic forms, not one
of which explains to what modification this or the other structure
can be ascribed. In order to decide these questions investigationa
concerning their transformation into one another were carried out,
and furthermore also measurement of the dipole-momenta was carried
Card 1/2

2o-6-34/59
On the Structure of Hydroxamia Acids and some of thair Derivatives
by means of Infrared Spectroscopy.
out according to SIDGWICK. Transformation into one another in the
case of heating of the a- and 8-forms were not observed. Under the
action of nitrogenous solvents (pyridine, nitrobenzene, aniline,
and ohinoline) the transformation of the less stable B-form into
the a-form was detected, so that in certain that they are not poly-
morphs. Investigations of the infrared absorption spectra prove the
existen*on of a group with an oxygen atom affized to carbon by means
of a double binding. (4 illustrations, 2 Slavic referencee)
ASSOCIATION: Charkov Zootechnical Institute.
PRESENTED BYt A.N.NESMEYANOV, Member of the Academy.
SUBMITTED: 12-10-1956
LVAILABLEs Library of Congress
Card 2/2

AUTHOR., USOVA,I.IL VOROSH31i T9.X. 20-1-33/64
TITM TH8 Frobi oncerning the Structure of Benzhydroxame Acids and
Some of their Derivativets. (K voproau o stroyenil benz idrok
samovykh kislot i nekoto:rykh ikh proizvodrWkh, Russianf
PERICOICALS Doklady Akademii Nauk S33R, 1957, Vol 114, Nr I , pp 120-123
(U.S.S.R.)
ABSTRACTs For the determination of the structural peculiarities of benzhy-
droxame acids and of the q 9 A-form of tri-beazhydroxilamine
(in the liquid phase) byestigations were carried out of the ab-
sorption spectra in the ultraviolet damin of the benzamid solutions
the mono- and di-berizhytiroxame acids, as well as of the C( , 0 -forms
of tri-bewhydroxilamino. Investigation of the electron spectra of
the solutlAm of the aftrementionea compounds was carried out by the
method of ultraviolet spectrography (according to V.HMI) with the
spectrograph ISP-22. This effect produced by concentrated 96%
sulphurio aoid on benzmnid oausoa a aecond absorption band and an
increase of the intensity maximan of absorption. The and re-forms
of tri-benzhydroxilamine in an ethanol solution and of the sodium
alcoholates have different spectra.
A different spectrum is cbtained by the C11 ~-form of tri-
benzhydroxilsm6ne in ocnoentrated 96% sulphurio acid. In the spectra
Card 1/2

2o-1-33/64
The Prdblem Concerning the Stmoture of BewhyAroxame Acids and
Some of their Derivatives.-
of the solution of these foms in sulphurio acid Various l1nes
vanish and they have nearl~r the same absorption maxim.
As found by experiment. both forms of tri-berX75hydroxil&Wine are
transfomed into di-benftdroxeLm (and benzo-)aoids under the
influence of concentrated sulphurie &aide. (With 3 Diagram).
ASSOCIATION: Not given
B T.-
SUBMITTED:
AVAnJBIM Library of Congress
CRzd 2/2

ARTEMOVA, V. M.; USOVA, Ye. M.
Effect of food coloring substances on the formation of the
gelatin structure. Izv-vysoucheb-zave; pishch-tekh.no. 2:
46-48 164. (MIRA 17:5)
1. Donetskiy institut isovetskoy torgovli, kafedra organicheakoy
i fiziko-kolloidnoy khimii.

LITOV, G. S.; 22!~~
Plague outbreak'among iarmot'hunters in ihs vicAitir"of Uk-
Golyn-Ulan-jima. lsv.1i,.,k.goo.nauch.-isel.protivochum.list
20tlll-115 '59. (Mi;; 1.3-.6)
(URT-GOLYN-MAN-KISA (MONGOLrA)--PTAM)

)Qbt&'kN0V, prof.; MiUVA, Yu.I., ordini.~tor
Some qllestion3 Of the epidemiology, ~r:lintcal courne and, theran.-?
of neurwiral diseaRes in the White lussian S.S.R. Zdra,7.173elor.
5 no.6:6-8 Je '59. (14IRA 12: ())
(wilm, 1IIjssIA--)"'IIcEPIU'LwIs) (VIR113 DI6T'Rs:';:3)

USOVA I Y11. I. [UsfAva, IU. 11 1
C)pper contcrit of the blood in meningoencephal, I t .'s "n c r.- -- .4rEr. .
Veatsi Ali BIS"'R. St.-r. bilal. nav. no.2:8,3-87 164.
17:11)

USOVAj Ze V.
Dissertationt "Midge 6f the Fmily Simuliidas Deptera of the Karelo-Firmish SSR
and Xurmanskaya Oblast,ff Cand Biol Sci, Inat of Zoology, Acad Sci USS4 Jan-Yar 54,
(Vestnik Akadwdi Naukv Moscow,, Aug 54)
SO' SUM 3939 26 Fab 1955

USOVA" Z. V.
I - Entomology
Dissertation: "'Inats of the Karelo-Finnish SSR and the Hurransk Lblast." ' &rd Biol
Sci, Leningrad Zoological Inst, Acad Sci USSR (no date of defense given).
(Leninskoye ZnanVa. Petrozavodsk, 21 Mar 54)
SO: SUM 213) 20 Sep 1954

USOVA, Z -V.
Biology of the pupal stage of gnats (Simullidae). Doki. Al SISIM
105 no.4:846-847 D 155. (KLRA 91j)
1. Institut biologii Karelo-Ifinskogo filiala Akadmii nauk SSSR.
Predstayleno akademikom To. N. Pavlovskim.
(Black flies)

V
USSR/Zooparasitology Ties and Insects (risesse-2mumitters) P-3
Abs Jour : Referat Zhur - Biologii, No 16, 1957, 70212
Author : -Usova, Z.V.
Title : Some Results of Testing the Action of DDT and
Hexochlorane on Black Flieu (fam. Similiidae) under
Lab. Conditions and in Nature.
Orig Pub ; rokl. AN SSSR 1956, No 2, 417-420
Abstract : A stream covered 50Cm by larvae and pupae of black flies,
chiefly Eusimuliuia latipes and S. truncatum, was treated
with a 20% oily concentrate of MIT for 25 minutes by a
final dilution of one to ten thousand. In 30-50 minutes
all larvae separated from the substrate. Yhnj larvak-
connected by threads in the water, disappeared after
twenty hours. Observation of the stream in 1955 shovc-d
new species of black flies, which were at the time or the
stream treatment in the forms of Qggs. The destruction
of different specleG of black flies was observed by
Card 1/2 - 4o -

USSR/Zoolarasitology - Tics and Insects (Diseusc~ Transidtter,_) P-3
Abs Jour Referat Zhur - Biologii, No 16, 1957; 70212
treatment of the same stream and its spring with a 20%
hexochlorane in a one to a million solution. Aluit
black flies which came in contact with the skin of a
calf lightly painted by a 2% cirulsicn of hexcehlorune,
containing 23-28 and 84.6% -isomere appeared to be ex-
tremely sensitive to these poisons, particularly the
hungry males. The abdomn, chest and neck of the horse
was lighly rubbed with a 2% ~:mulsion of hexochlorane.
It tcok 18-20 hours until luolated rules sat there; they
perished in 5-6 hours, Within 40-48 hrs. on and around
the tested horse there was one half of the blackflics
than on the control horse.
Card 2/2 - 41 -

USOVA, Z.V.
....
Materials on the biology and ecolog7 of the black flies
(Simultidae) in the Xarelo-Finnish S.S.R. and hirmansk
Province. Trudy Kar.-Fin. fil. AN SSSR no.4:131-149 156.
(HLRA 10:2)
(Karelia--Black flies)
(Marmanak Province-Black flies)

USOVA, Z.V.
- ~1-7Y
- kology MA ecology of black flies (Dipters, Sivmliidae) in rarelia
and Murmansk Province. Int.oboz.35 no.4:840-855 '56. (KM 10: 2)
1, Institut biologil ]Larellskogo filiala AN SM, Petrozavodek.
(Karelia-Black flies) Nurmansk Province-Black flies)

USOVA, Z.V.; XMIROVA, Z.F.
Bloodsucking activity of black flies (Diptera, Stwilildae) in
Zarelia [with summary in Ingliahl. Ent.oboz. 37 no,4:869-882
158a (MIRA 11: 12)
1. Karellskiy filial AN SSSR, Petrozavodsk.
(Zarelia--Diptera)

USOVA, Z. V.
"Daytime Hiding Places for Mosquitos and 1,1idges (Deptera, 51muliidae)."
Tenth Conference on Parasitological Problems and Diseases with Natural
FWservoirs, 22-29 October 1959, Vol. II, Publishing House of Academy of
Sciences, IISSR, Moscow-Leningrad, 1959.
Institute of Biology, Karelian Branch of USSR Academy of Sciences
(Petrozavodsk)

- TJSOVA, Z.V.
Searching for new methods 6f controlling the water phases of
the black flies (Diptera, Simillidae) in brooks and rivers of
Karelia. Trudy Kar.fil.AN SSSR no.143114-123 159.
(MW 15:12)
(Karelia Black flies-Extermination)

USOVA, Z.V.
- - I
A new species of black flies Hellichia dogieli n. sp. (Diptera,
Simuliidae) from the Kare2lan A.S.S.R. Trudy Xar.fIl.AN SSSR
no.140.10-113 059. (MIRA 15:12)
(Karelia-Black flies)

USOVA Zinaida Vasillyevna -M-1, Y.A., kand. bioIog. nauk., red.; gflEj,
- - __ - 1__ BF77
~~~Xov) ZjL , ~Z izd--;-Ta,, U-NDELI, ~.Ye... takkir. red.
[Black flieo (Diptera, S!nulii(lae) of Karelia and MumArjack Frwilwe I
Fauna rioshek Karelil i Murmanskol nblanti (Diptera, Simliladae').
Moskva, Izd-vo Akad. nauk SSSR, 1961. 286 p. (MIRA 14~,12)
(Karelia-.-Black flies) (Mijimanol, Province, -31ark flies)

-- - --- -- - I
~W30VA, Z.V.
Materials on the biology of adult black flies (Diptera, Sirmll i-idae)
in the Karelian A.S.S.R. Paraz. abor. 20z299-305 161. (HIPA 14:9)
1. Institut biologii Karel'skogo filiala AN SSSR.
(KAMLU--BLACK FLIM)

USOVA, Z.V.
Phenological periods and duration of the development of
black flies (Diptera, Simullidae) in the Karelian A. S. S. R.
and in Murmansk Province. Trudy Kar. fil. AN SSSR no.30:143-152
161. (MM 15:9)
(Karelia-Bla* flies)
(Murmansk Province-~-Black flies)

US(JVA,-LY-,,,-
A now and some little known species of black flies (Diptera,
Sirmlliidae) from the Karelian A. S. S. R. and Murmansk Province.
Trudy Kar. fil. AN SSSR no.30.153-160 161. (MIRA 15-9)
(Karelia-Black flies)
(Murmansk Province-Black flies)

USOVA, Z.V.
Hiding places of black flies (Diptera, Simuliidae) in the Karelian
A.S.S.R. Ent. oboz. 1+2 no.2:316-319 163. (MIRA 16.8)
1. Institut biologii Karel'skogo filiala AN SSSR, Petrozavodak.
. (Karel-ia-Black flies) (Insects-Behavior)

USOVENK09 V. V.
"Visoosite des systernes acide acetique -- dimethylaniline et acide acetique --
dietbylaniline".1 Udovenko, V. V. (p. 1923)
SO: Journal of General Chemistry (Zhurnal Obshchei Khimii) l9hOj Volume 10., no. 19-20.

-USS07-1=1=1 I
4475. 1 -o Aro 1.11"ye ..."ofty-moy
1 5! - a.
pron,,shlenriosti v 1953-~4 (103. Y., 73t.?! i"i
5 Ill. 20SY.. 1.000 el=. 65F.- (54-5P026)
622:323:621.3
SO: Kr.!zhn't,,ra Letopsial, Vol. 1, 1955

Us OvTRSHFINS Tvov,~,,N I YF,
4516. TekhnologicheskiM Prots6:-,sov Sverki. ( 9bornil- 3tatyey). M., 1954.
12 S. S. Ill. 20 sm. Trnnsp. Mashinostrayeaiya S331R. 'Isye.,,oyuz. Froyektn-,-
'0
Tekhnol. In-t Ypti. Obcien Tekhn, Listok No. 12). 5ne Frz. P. TS.- (5,-15,~,,58 Zb)
621. 941-7
SO: Letopis' ZhurnalInykh Stateyo Vol. 37. 1949

LEBEDEV, P.T.; USOVICH, A.T.; CIEFUR011, L.P., prof.; KALICHERKO, M.M.,
aspirM; WMEV-7ull, V.P-ej doktor vev-rin. nauk; STERIKO., A.S.$
mladshiy nauchnyy sotrudnik; LAKlffffTKINA, A.N., aspirant;
GRISHCHOKO, N.F.; ORLOV, A.I., veterinarnyy vrach (Arkhangell-
nkaya obl.); PROSTYAKOV, A.P., kand, biolog. nauk, KOVYNDIKCV,
M.S.,, kand. veterin. nauk; ARUTZHANOV, K.A., kand. vaterin. nauk
Veterinary experiments. Veterinariia 41 no-4:101-111 Ap 164.
(MIRA 17:8)
1. Sibirskiy nauchno-issledovatellskiy veterinarnyy institut
(for Lebedev, Usovich). 1. Poltavskiy seltzkokhozyaystvennyy
institut (for Chepurov, Kallchenko). 3. Ukrainskiy nauchno-
issledovatellskiy institut zemledellya (for Matusevich, Stenlko,
Lakhmytkina). 4. Cherni ovskays. oblastnaya veterinarnaya. labwa-
toriya (for Grishchenko~. 5. UkralnskLy nauchno-issledovatell-
skiy institut eksperimental"noy veterinarii (for Prostyakov,
Fortushnyy, Kovyndikov). 6. Uzbekskiy nauchno-issiedovatAllskiy
veterinarnyy institut, (for Arifdzhanov).

USOVICH, N.V. (Molodechnanskaya oblast')
Some more remarks pertaining to the universal board. Hat. v 9khole
noo5:65 S-0 160. (MIRA 13tIO)
(Geometr7--Visual aids)

USOVNIKOV V.I.
Kirov Plant is a laboratory for new equipment. MaBbinoetroitell
no.9:4p-5 S 161. O-MU 14:10)
1. Predsedatell proizvodstvenno-massov9y komissii zavkoma Kirovskogo
zavoda.
(Leningrad-Machinery industry)

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J. Grvc. CAwm, 13, tAW-d
"S kming itviteral lirmvdare wa4 umd lor
Ividatkin -it subalifultil l(gurms by Ninflit: dild. INS0.
atod the t,Jttetir were vipwivittly itirml and 4owly freated
fih& MI.A. 11.0, aft'l Mm),; the 111A.4 wa. thris
'filirml. wa.'Iff4l. $md toppid, ff."11 alk. .40. by IIL'I
IV) Mu0t, anti 176 s, timn. vicied. litW). at 1111' low 16-19
go bro.' gave 2,44sirklirwobtawir deid (nit m.p,).
IiPS0. (75 s., 7"11%). 20 S. 2-clittwo-1 -nit rutriluene, IMI
A. Nln0i, and IM) S. cvm. coned. 110). trairr in 17 firs. at
so 17.5' (75* ???) 70-51",, drid itti,p.
1101L givitit). 11,S04 (75 g., 59",4, 24) g. _f-ultrotolurne.
'111 it. W04. anti I&I S, taim. emM. 11.40. pvv 80-2'-,
~~.Iafbrmxoir mrW in 3.5 -1 hirs. at 135-0' and 74-45% at
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RC~Ardl 1113t., NIO~:OW)- J. GCX. CACM. V.S.S.R. 19.
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with Ice gave 5.mdhozy-6-xitrip.x."dylbrxstgriasok. m.
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FILIDKAS, I.Kh.; USOVSKATI, V.S.
Thiosemicarbasones of certain aldehydes and ketones. Soob.o
nauch.rab.chl.VIRO no.3:45-46 '54. (MIRA 10:10)
(Somicarbason-es)

Al //V
V
USSR/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abst Journal: Referat Zhur - Kh1miya, no 19, 1956, 61543
Author: Rubtsov, M. V., Nikitskaya, Ye. S., usoxt~zry_a~,V- S
Institution: None
Title: Alkamino Esters of Some Heterocyclic Acids as Possible Hypotenaive
Remedies
Original
Periodical: Zh. obahch. khImii, 1956, 26, No 1, 130-134
Abstract; There have been synthesized the diethylaminoethyl eaters of dipico-
linic (1), dipipecolinic (II), N-methyl dipipecolinic (111), 6-
methyl--picolinic (IV), 6-methyl pipecolinic M, 1,6-cimethyl
pipecolinic (VI), and quinuclidine carbo*lic-2 acid (VI-I). On
pharmacological investigation it was found that the cli-methyl
iodides of VI and VII have high gEuiglion-blocking activity. A
mixture of 3'~g dipicolinic acid (W][II) and 30 ml SOC1 is boiled
until completely dissolved (48 haxwe) heat the thus Pormed di-aid
chloride (1K) with 30 ml diethylam:Lnoethanol (X) for 6 hours at
Card 16'

USEIR/Organic Chemistry - Synthetic Organic Chemistry, E-2
Abst Journalt Referat Zhur - Khimiya, No 19, 1956, 61543
Abstracti 110-1150; 1 is obtained with a yield 55.4%., BP 214-2150/0-5 mm;
dibydrochloride MP 190-191 0;-dimethyl iodide MP 200-2020. Analo-
gously frm 6-methyl picolinic acid (XI) is obtained IV (yield
'T7%, BP 128-1310/0.25 mmi hydrachloridep MP 147-149oj methyl iodide,
MP 115-1170) and 4M quinuftdine carboxyl-tc-2 acid, there is ob- '
tained VII; yield 73%j, BF 166--1640/9 mm, difethyl iodide MP 222-223'
(from acetone). 10.7 9 of I are hydrogenated in 165 ml of 2-5~
solution of HCl in alcohol (o.63 9 PtO2 -2o0, 40-60 cm of water
column, 9-10 hours); water is adjpd ., the mixture is filtered,
evaporated to dryness,, treated wIth 50% solution of K2COj and ex-
tracted with ether; 11 is obtained with a yield 86%, BP 182-i840/o.2
mmj trihydrochloride MP 232-2330. Analogously is prepared V, yield
52.3%, BP 98-1000/0.2 mmj dihydrochloride MP 2200. By boiling of
IX with absolute alcohol is synthesized the diethyl ester of I
(XII), yield 84.7%, BP 127-1280/0.2 mm MP 44-460. Analogously is
prepared the ethyl ester of XI (XIII), yield 87.3~, BP 79-.810/C.25
mm3 hydrochloride MP 74-750. By hydrogenat ,ion of XTI and XIII over
Pt (from PtO2) linder the above-described conditions are obtained
respectively the diethyl ester of dipipecolinic acid (XIV), yield
Card 2/3

USSR/Organic Chemistry - Synthetic Organic Chemistry., E-2
Abst Journal: Referat Z+ - EhimiYa., No 19,, 1956, 61543
Abstract: 90%, BP 103-1050/0.25 mm, and the ethyl ester of 6-methyl
pipecolinic acid (XV), yield 92%, BP 99-1000/13 mm; hydrochloride
MP 213-2150. Mixture of 4.27 g XIVI 1-32 g CH3J and 23 ml abso-
lute alcohol heated for 6 hours at 40-450, evaporated in vacuum,
residue extracled with dry C6H6, the insoluble hydroiodife of XIV
is filtered off and from the benzene extract is recovered the di-
ethyl ester of N-methyl dipipecolinic acid (XVI), yield 52.7%, BP
107-VO/0.2 mm. Analogously is prepared the ethyl ester of 116-
dinethyl. pipecolinic acid, yield 43.* BF 53-540/0.2 no; hydro-
chloride MP 198-2000. In 7 ml. of X are dissolved 0.01 g Na, added
with stirring 1.32 g XVI, heated 3 hours at 1500 (distilling off
the alcohol) excess of X is distilled off, the residue is treated
with 50% solution K2CO3 and extracted with et$W; III is thus ob-
tained, yield 51.2%, BP 176-1780/0.2 =j methyl. iodide and hydro-
chloride are oily subs Analogously is synthesized VI
yield 44-7%, BP io6-1;~"0.2 mm; d-imethyl iodide MP 201-2026.
Card 3/3

Y,c~-
f7'
AUTHORS: Ilikitskaya, Te. S. , Usovaa:aya, Y. 0, , Rubtsov,M. V. 79-1 -341"A
TITLE: Tertiary Amines of Some Nett~rocyclic Compounds as Pcosible-
Means For Blocking lNerve GanGelia (Tretichnyye aminy nekot-or-
ykh eeterotsiklov kak vcizmozlinyye gi,,L)otensivnyyp- sreds-1-ra),
PERIODICAL: Zhurnal Obshchey Khimii, 1958, Vol. 25, Nr 1, pp. 161-166
(USS'i).
ABSTRACT: The quaternary ammonia salts with their quaternary nitrogen
were formerly considered the most important source of re-
medies for blocking ganGlia. But the most recent investigat-
ions showed that this may also be the case with secondary and
tertiary amines (reference 2). Thus the authors %ad already
earlier found that e.g. the pertinent 2-diethylaininoethj1-
1~ aminomethylquinliclidine (formula (a) ) possesses a high ac~iv-
ity in the above-mentioned serise. As compounds of this typer
of activity are of Great impor'ance for healing hypertonia it
was expedient to synthesize simpler compounds of a similar
type, namely that of the pyridine and piperidine sctries. By
the conversion of the hydrochlorides or esters of dipicolnj~,
and 6-methylpicolinic acid with different amines it was
Card 1/2 possible to produce the amides (I and II). In spite of

Tertiary Amines of Some Heterocycli-_ Com-cunds as Possible 79-1 3.:'A~
Means For Blocking Nerve Ganglia,
indications in publications that no anines can be obtainei
from the amides of pyridincarboxylic acids with the aid of
the aluminum hydride of lithium the authors succeeded ir con-
verting most of the obtained amides to the amines (III)
although the yield on that occasion %7&s small and by-products
occurred. The reduction of the amides of piperidincarboxylic
acids took place much better, vrith good yield6 and easy iso-
lation (IV). The pharmacologi-.al Investigation of the pyrid-
ine and piperiding derivatives which was performed by 1. 114.
Sharapov showed that 1,6-dimeth,,fl-2-(P-dietl-,.ylaminoethy'---
aminomethyl)-piperidine (IV d) possesses a high activity 14n
the above-mentioned sense, that it even ten times surpas3es
that of tetraethylammoniumiodide. There are 1 table and 6
references, 5 of which are Slavic.
ASSOCIATIOL. AU Uslan Scientific Chemical-Pharmaceutical Institute ineni 5
Ordzhonikidze (Vsesoyuzayy nauchno-issledovatellskiy khimiko-
-farmatsevticheskiy institut imeni S. Ordzhonikidze)
SU31UTTED: January 7, 1957
AVAILABLE: Library of Congress
Card 2/2 1. Chemistry 2. CY01ic compounds 3. Amides

AUTHORS: llikitskava, Ye. S., Usovskaya, V. S., SOV/79-29-1 -2-31/7,4
Rubtsov, M. V.
TITLE: Bicyclic Systems Derived From 2,6-Lutidine (Bitsiklichesl-iye
sistemy na bnze 2,6-lutidina)
II. Synthesis of the 3,9-Oxazabic.-,-clcl-[3,,,,l]-Nonano and Its
N-Derivatives (II. Sintez 3,9-oksazabitsiklo-[5,3,1] -nonnna
i yego N-proizvodnykh)
PERIODICALs Zhurnal obahclioy khiiniif 1959, Vol 29, Tir 1, pp 124-129 (USSR)
on
A13STRACT: In continittng wark/lhe synthesis of the bicyclic systerns derived
from 2,6-lutidine the authors obtained a new compound, the
3,9-oxazabicyclo-(3,3,1)-nonane
CH CH CH2
6- 4
CH2 1111 ~3 0
CH2 CH C112
Card 1/3 The diethyl ester of the dipipecolinic acid, obtnined from

Bicyclic Systems Derived From 2,6-Lutidine. SOV/79-29-1-28/74
II. Synthesis of the 3,9-Oxazabicyclo-[3,3,11 -11onane ani Its 1;-Deri-,atives
2,6-lutidine, was used as initial product (Ref 1). By the
reduction of the ethyl ester of this acid with aluminum-lithi-
um hydride in ether solution compound (I) was obtained which
yielded (II) by methylntion. By the action of thionyl chloride
in the hydrochlorides of M and (II), (III) and (IV) were
formed. On longer boiling of M with sulfuric ncil (V) result-
ed, a slightly volatile, crystalline and salt-forminq product
(on nitrogen), from which some ofitsN-substituted derivatives
were obtained. From compound (I) the nonane (VI) was formed by
formic acid and formaldeh-,'de. The sulfurization yielded the
N-sulfo acid which was separated in the form of potas~3ium
salt (VII). By the repetion of (I) with the chloric acid
anhydride of /3 -chloro propionic acid in alkaline medium with
subsequent boiling of the resulting amide of this acid rith
piperidine and diethylamine the compounds (VIII) and (IX) were
formed. By reduction of the Pmides obtained with aluminum-
-lithium hydride (X) and (XI) were synthe31ZOd. The reaction
of an excess of (I) with dichloric acid anhydride of P.1utaric
and ndipic acid the diamides (XII) and (XIII) were obtained.
Card 2/3 The latter were transformed by reduction with aluminum-lithium

Bicyclip Systems Derived From 2,6-Lutidine. SOV/70-29-1-2e/71
11. Synthesis of the 3,9-0xnzabicyclo-[3,3,1] -!Tonane and Its J-Deri,,ati-,er,
hydride and subsequent treatment of the resultin,-, amines with
methyl iodide into the compounds (XIV) and (XV). Compound3 (V)
and (W show a nicotine-like netivity, whereas compounds
(VIII-'XI) e.,.,-ert a lo,.,ier activity. There are 2 references, 1 of
which is Soviet.
ASSOCIATION: Vsesoyuznyy nauchno-issledovntellskiy 1-himiko-fnrmatsevti-
cheskiy institut imeni 'J. Ordzhonikidze (All-Union Chemico-
pharmacautical Scientific Research Institute imeni S. Ordzho-
nikidze)
SUBMITTED: November 30, 1957
Card 3/3

SOV/7 9 - 29 - 2 - 2 5/7
AUTHORS: Ni4kitskaya, Ye. S.,,Usovskaya, V. S., Rubtsov) Y. V.
TITLE- Piperidine Derivatives as Possible Hypotensive Agents (Prc~izvcd-
nyye piperidina kak vozmozhi,~yye gipotensivnyye sredstva)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29# Nr 2, PP 4'12--476 (USSR)
ABSTRACT: According to the see tertiary amines of the quinuolid-ine and
piperidine series, which develop a high ganglion-blocki-,~
activity, the authors synthesized some N-substituted ,.pezidins
derivatives, in order to exi3mine further tertiary amiras,
2,6-lutidine, a waste product in the preparation of "I ht-hivaz-,-"a"
(Ftivazid), served as initial product. The reaction o" 2,6-
lupetidine (obtained from 2,6-lutidine) with the chloric an-
hydride of P-chloropropioni3 acid and subsequent boiling of thp
reaction product in ethyl alcohol with piperidine and diethyl
amine gave the compounds (I) and (II). By reduction, 'the latte:-
correspondingly passed over to compounds (III) and (IV) (Shemei
After a number of failures, the authors succeeded in carrying
out the synthesis, beginning from 2,6-lupetidine, of the se(,
quaterna=y salts by the aid of dichloric anhydride of glutari-c-
Card 1/2 '
and adipic acid; namely, compounds (V) and (VI). These

Piperidine Derivatives as Possible Hypotersive Agents
SOV/7 9 -29--2 -2 rl,/'71
piperidi(~es of both acids could, correspondingly, be
by redui~,tlion into 1,5-bro(21,61-dimethyl piperidine,--14)--pentari~
(VII) and 1,6-bizs(29,61-dimethyl piperidine-19)-hexane (VI11)".
See quaternary salts (Scheme 2) easily result from these tw-
compounds. By reaction of ethyl eater of 6--methyl pipecclin-i"
acid with ~~hloric anhydride of 0-chloro propionic acdd and by
subsequp.~,t treatment of the reaction product with pipez-dine
or diethyl amine, piperidines (IX and X) ware z~btained,
ir their turn changed over to piperidines (XI and XII) by
red-action (Scheme 3). The constants of the c1cmpciands eynthe-
sized will be given in a following paper,, There is 1 Sov,-et
reference.
ASSOCIATION: Vsesoyuznyy nauchno-issledovatellskiy
institut 1-meni S. Ordzhonikidze (All-Union Scientific Chemo--
pharmaceutical Research Institute imeni S. Ordzhonikidze/
SUBMITTED: January 3, 1958
Card 2/2

RUBTSOV, 14.V.; IIMTSIUYA, Ye,S.,- MMU, A,D,; USOVSKAIA, V.S.
New ganglion blocking preparations. Khim. i med. no.15;16-28 160.
(ML-iA 15: 1)
1. Vsesoyuzn3rf nauchno-issledovate.*Ilskiy khimiko-farraatsevticheskiy
institut imeni S. Ordzhonikidze.
(AUTONURIC DiWGS)

5.3610 77375
SOVIN-30-1 05/~8
AUTHORS: NikJtskaya, Ye. S., Q~
Ovs~(aYa, V. S., Rubtsov,
.
M. V.
TITLE: Bicyclic Systems Based on 2,6-Lutidine. III.
N-Derivatives of 3-Oxa-g-azableyelo-(3,3,1)-Nonane
PERIODICALi Zhurnal obshchey Ichiinii, 1960, Vol 30, Nr 1, pp
171-182 (USSIJ)
ABSTRACT: Acyl and alkyl derivatives of 3-oxa-g-azabicyclo-
(3,3,l)-nonane (I) were synthe3ized. Acid chlorides of
acetic, propionic, and benzoic acids were reacted wJth I
in anhydrous benzene with cooling and 9-acetyl-
(Ila), 9-proplonyl- (Ilb) and benzoy-L-3-oxa-g-aza-
bicyclo-(3,3,1)- nonanes 4Ic) were obtained. The ob-
tained products, on reduction with lithiwa alum'Lnum
hydride, were converted Into :orresponding amines.
Morpholine and dimethylamine in anhydrous aicohol,
phenothiazine in anhydrous benzene, and the .-odium
Card 1/10 aalt of quinozolone-11 in anhydrous alcohol werq

Bicyclic sy3tems Based on 2,6-Lutidine. 111 77375
SOVI~9-30-1-36178
reacted with 9-( cliloropropionylA-3-oxa-9-azabicyclo-
(3,3,1)-nonane afCal-corresponding -substituted deriva-
tives of 9-propionyl--3-oxa-g-azablicyclo-(3,3,1)-nonanes
(IId, IIe, IIf, IIg) were obtained. The above reaction
with phenothiazine and quinozolone takes place with
formation of a aideproduct, 9-acryloyl-3-oxa-g-
azabicyblo-(3,3,1)-nonane.
0 N ~-CH=CH2
Acetyl chloride reacts with I, in aqueous alkali,
forming as main roduct 9- [31-oxa-91-azabicyclo-3',
31, 11-nonano-9 I -a(l,etyl-3-oxa-g-azabicyclo-(3,3,1)-
nonane (IIJ).
Card 2410

Bicyclic Sy3tems Ba3ed on 2,6-iuti(tine. 111 77-375
Solj/~ q
(0) (OCH
EKIMS
("IR cucor,
(J) R WHICHIK, 70
(e;R-ccc",cHjp(c",h
R- COCHLCHt
asu
RNCOWHI), COOR
0
H
- ON'
N
0,
R COCRICHL,
N
i;)A-cmm,N~D
(Voccoc", -
K-10
R
~11
N'
0
W [;.C'H'
(it; A c w?
(a)

n-1 A C,H,
(qn.z R- CtHs
(C)n-3 R. CMS
Card 3/10

Bicyclic Systems Based on 2,6-Lutidine. 111
(CQ,OR
N
4
0
~O
IV)
n:3
~p 4
77375
SOV/7 9 -31 O-i -36/78
0
ph:3
n 4
011)

PL N

4
~" OC,Hi
Card 4/10

B.IcycliG Syo,;ems Based on 2,6-Lutld.ine. 111 77375
S OV/7 9 -30 -3 6/7 8
The corresponding amines (110, IIP, IIr, IIs, IIt)
were obtained on reduction of IId) He, M) IIJ, Ilk,
with lithium aluminum hydride. Attempts to reduce
compounds IIf and IIg were unsuccessful. The desired
amines were prepared as follows: I was reacted with
carbethoxyacetyl chloride. The obtained IIIa was
reduced to IVa; the latter with thionyl chloride gave
VIa. Phenothiazine and quinozol-4-one were reacted with
Vla; corresponding VIIa and VIIb were obtained. IIIb
and IlIc were obtained similarly from PO-carbethoxy-
propionyl chloride and /3-carbomethoxy oplonyl
chloride, forming on retFuction lVb. Tnionyl chloride
was reacted with IVb and a corresponding hydrochloride
(VIb) was obtained. Phenothiazine reacts with VIb,
forming VIIc(yield 34%).Alkoxides react with Vlb,forn:-
ing corresponding ethers. VIId and VIIe were obtained
by the above reaction.
Card 5/10

Bicyclic Systems Based on 2,6-Lutidine. 111
77375
SOV/79-30-1-36/78

, 11A11- H
QEACTIO

TVMFCRATViQK JELP
Y
(0/p 801UNC MIT

it M04) M(LTING POINT

YPROGHLORSOC
3 COC11 4 On &oll;At 67 - 200-2020
3 c0c,1
15 4 0- Wit;" 68 - 170-172
3 cocal1r, 4 On bo,*I,,,9 80 - 189-191
c0

:1 3 60-700 59 183.50 (0.9) 179-181

Go
45-50
72
18:1 (t)
150-151-1

(0ontinuation, and explanation of
Card 6/ 10 aeterlsk8, on next cards

Blc,,fclic Systems Rused on 2,6-Littidine.
Ctable cont'd)l
77375
SOVT9-30-1-36/~,

Y1
R PEAC-
r10N
TOW
14 $)P Rc A C T10fJ
TV4Pr4r,TVVC VjfLV
(0/,) COILINC P011fr
(pitrtsucc it;

ti ot) bqCLTMC r0jj~
or

MoFoc"Lovic
c0cll 4 On 11011"nq 95 201-202
COG,1~, 4 On baffinq -100 494-196
4 ,
cocall, 4 On hoiling 87 194-195-5
co-1
2 60 67 200-2101 y).8j 137- [39

152-154
\Wy
Was isolated In the form of d1hydrochloride.
Was isolated In the forn of dihydrochlorlde
monohydrate.
Card 7/10

Bicyclic Systems Based on 2.6-Lutictine. 111 77375 'P
SOV79-30-1-36/17 ~
The yields and propertiesof compounds are given below:
Compound Yield bp ('C) (1,ressure mp (0C)
(%) in mm)
IIa 0
1 io6-log/j.
Ilb 0 113-114/p.6
IIc 81 162-163/0-7
IId 72 183-185/0.2
IIe 75 140/0.8
I
1st fraction t-%-#30 101-103
IIf 2nd fraction
M
j 5*6 26o
IIg 27
IIh 8 124-126/o.5
Iii ~3 157-159/o.liz
IIJ 0 148-150~o.7
IIk ~3
111 81 67-67-5/3
IIM 64 55-56/0.8
Iln 93 119-121/0-7
Card 8/10
74-75
-
78-80
-
68-70
138-139
77-79
97-99
100-102
14o-i42
38-40

Dicyclic Systems Based on 2,6-Datidine. 111 77'375
SOV/79-30-.l--,6/78
(Continued from Card 8/10.)
The yield and proper-ties of compounds are given below:
Compound Yield bp (00) (Presoure mp (00
M in mrrt)
110 72 14o-142/0.6 -
IIP 62 98-:Lcio/b.6 -
IIq 79 .108/0 .35 -
Ur 0
N 118-120/0-3 -
IIS - 113-115
IIIa 77 157-159/0-7 -
IlIb 55 151-152/0-5 -
Me '(7 171-172/1 63-65
IVa 65 107-109/0-5 -
IVb 70 135-137/1
Vla 75 217-219 (dec) -
VIb 8o - 1-73-175
VIIa 41 - 234-236 (alc)
VIIb 52 215/0.8 -
VIIC 34 - 194-196
HM 9/10 - 163-165

Bicyclic Systems Based on 2,6-Lutidine. 111
(Continued from card 9/10.)
VIIe 64
77375
SOV/79-30-1-36/78
176-177
There is 1 table; and 1 Soviet reference.
ASSOCIATION: Ordzhonikidze All-State Scientific Research Chemical-
Pharmaceutical Institute (Vsesoyuznyy nauchno-
issledovatellskiy khimiko-farmatsevticheskiy institut
imeni S. Ordzhonikidze)
SUBMITTED: January 21, 1959
Card 10/10

MITSKLU, Ye.S.; USOVSYAU, V.S.; RUBTSOV, Mv.
Bicyclic systems based on 2., 6-lutidiue. Part 5: Biquaternary
salts of ajLv -bis[9-methyl-3, 9-diazabicyclo (3., 3.. I)-nonano-31-
n1kanes. Zhur.ob.khIm. 31 no.10;3202-3205 0 161. (KRA 14:10)
1. Voesoyuznyy nauchno-iosledovatellskiy khIml -farmateevticheakiy
institut imeni S.Ordzhonikidze.
(Lutidine) (Paraffins)

NIKITSKAYA, Ye.S.;-gSOVSK~ ~,V.S.; RUBTSOV, M.V.
Bicyclic compounds based on 2j,6-lutidine. Part 4: 3-Substituted
derivatieves of 9-metbyl-3,,9-diaza&cyclo [3.3,ljnor,-qne* Zh=*ob&
khim. 30 no.20:3306-3315 0 161. WIRA 14:4)
(Diazabicyclononane)

NIKITSKAYA., Ye.S.,- USOVSKAYA, V.S.; RUBTSCV, M.V-
Bicyclic systems on the basis of 2.6-lutidinE!. Part 6: Synthesis
of 3,9-diazabicyclo D.,411nonane. Zhur.ob.khim. 32 no.9:2886-2E88
s 162. * (MIRA 15:9)
1. Vsesoyuznyy nauchno-issledovatellskiy kh].miko-farmatscvtichoskiy
institut ineni S. Ordzhonikidze.
(Bicyclononane)

NIKITSKAYA, Ye.S.; !LS~~tSXAYA, 1~.S,; RUBTSOV, M.V,
Bicyche systemo on tho banis of 2..6-lutidins,
Part 7; Interaction of alkyl (aryl) M"sium
halides with benzylimide of N-methylcUpipe colic
acid. Zhur.ob.khim. 32 no.n:3687-3693 N 162 .(MIRA 15:11)
1. Voesoyuznyy nauchno-issledovateltakiy immmop
.farmatse-.rticheBkiy institut imoni S. Ordzhonikidze.
(Pipecolic acid)
(magnosium organic empounds)

I
RUBCOV) M.V. [Rubt3ov, M.V.1; SAAFOV, I.M. (Sharapov, I.M.jj MASKOrSKIJ,
M.D. (Wahkovakiy 140.1; HICH-LINA, Me (Mikhlina, Ye.Ys.];
NIKITSKAJA, E.S. tflikitskayu, Ye.S.); VOROBJEVAI V.Ja. (Vorobrfaiu,
V.A.); USOVSKAJA, V.b.-[Ubovskaya, V .S.).
P~ritb--iolm and pharmacoloLdoal x-esearch on quinuclidine, piperldine
and pyridl-r- derivati7es. Cask. fam. 13 no.6:299-315 J-1164
1. -v&iEcko--tyzkumny usta-T pro chemii a fwnac-li, M:):t*',:-,.re
(VIIICHPI) [Vsesovuznyyrtauchno-issl.edo-va-tellskiykbijr~Ko-farmat5iT-
ticheskiy institull.

NIMITSKAYA, Ye.S.; LFVKOYFVA, Ye.I.; USOVaAYA, V.S.; RUBTS97, X.V.
Synthesis of 7-hjdroyy-9-xk*.hyl-3,9-dia2abicyclo [3,3,11 nonans
and some of its derivatives. &ur. org. khim. I no.1:174-182 Ja
165. (,%Ilqli 18:5)
1. Vsesoyuznyy nauchno-IssledovatellskLy klitmiko-ftti,inatsevtLclierkiy Institut
imeni S.Ordzhonikidze.

"l-C, Ion Y Jlov a I i'll- 0 3!!
V. Illus.
'v I I -
T. -P. In En
a
L I b. 1951
1956

GIMINOVA, N.V.; KHASNOSSLISKAYA, T.A.Cdeceaned]; LIMVIH-.
Ye.Y., redaktor; TUKARKINA, N.A., tekhnichaski.V redaktor
[Inglieb-Russian agricultural dictioaaz7j Anglo-rusekii sel'sko-
khoziaistvannyi slovarl. Izd. 3-s. perero Moskva, Goo. Izd-vo
takhniko-teoret. lit-z7, 1956. 532 P. (MLRA 9:8)
(Inglish language--Dictian&rias--Rusetan)
(Agriculture--Dictionaries)

USOVSKIY, B., prof.
Por a greater variety of vegetables. Hauka i pered. or. v sellkhoz.
8 no.10:61-64 0 158. (MIRA 11:11)
(Vagetables--Varieties)

USOVSKITO B.
3xparlence in constructing poultry processing plants In the United
States. Miam. ind. SSSR 29 no-5:58-59 158. (MRA 11:10)
(United States--Poultr7 plants)

USOVSKIT, B,&,.. agronom; LINNIK, Te.F., agronom; PODKAKEINM, Tu.K.;
- .1 SHKOHIM, Z.1., kBnd.sellskokhos.nauk; 14SYSTUIOV, Tu.M., red.:
TUKARKINA, N.A.. tekhn.red.
[Russian-English agricultural dictionary] Rusako-angliiskii
sellakokhoziaistvennyi slovar'. Soat.V.N.Umovskii i ar.
Moskva, Glav.red.inostr.nauchno-tekhn.olovarei Fizmatgiz, 1960.
504 p.. (MIRA 13:10)
(Agriculture-Dictionaries) (Russian language--Dictionaries--Bnglish)

USOVSIIY. B., ycof .
. Kohlrabi and some other vegetables. Obshchosty.pit. no.l2t22 D
16o. (MIRA 13:12)
(Vegetables) ~14 (Cabbage)

USOVSKIY, 3,11., prof . (moskya)
Blueberr.v, Priroda 49 no. 12;98-99 D 160. (MIR-t 13:12)
(Blueberries)

~';~~-Pro~-
Artichoke is a culinary delicacy. Obsbehestv. pit. no. 1:50
Ja 161. (mm 14:1)
(Artichokes)

IISOVSKIY v B. p -:,,rof . k,
Leaky aa onion of a particular taote. Obahchesty.pit. no.2:25.-26
I1-1 7 161. f (MIRA 14:3)
(onions)
..4,
d. !.
~a ,
- N:

IJSOVSKIY B. -.prof,
Aromatic table vinegars, Obahchestv.'pite no. 3:23 My 14M.
(MIRA 14;5)
(Vinegar)

USOLUII.-B prof .
I
Arcmat-I.c table -salts. Obshchestv. pit. no.6:31 Je 161. (MIRA 14:9)
(Salt)

USCYVSKIY, B.N., prof. (Moskva)
Nov salad plants. Priroda 50 no.7:116-117 JI 161. (NM 14:6)
(Vegetables)

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00 mUings an &I--*--;nm wA copper. wW gives *IFM wAtirrings. Themolclerins
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tjsp~-';Ye. P.
Milky Way.
Now infrared radiation of tho Milky Way. fiz. nauk 46 no. 3, 1952o
9. Monthly List of Russian Accessions, Library of Congress, A~~t 195Y.2 Unclassif led.

U-!:-, ALIS) F.
5 0 T - 1". .11, E,
7EF7CD7C'11-L: DAM.I. SHRIJA B. TRUDY. S'RlIA -7. No. 3, 1958
Uspalis, K. Concerning the dielectronic juncti.ons In heliwn-type -.toms. In
Russian. p. 47.
Monthly list of East European Accessions (EEAI) LC, Vol. 8, Nc. 2,
Fel-ruary 1959, Unclass.

USFALISI K.
On integration of the Generalized radial jnterLr;1Is occurring irl the quantim thcrry
of the atom.
P. 45, (Lietuvos TSR YokSlu Akadc-mija. Fizikos-technikos institutas. Vol.
2:, 195,6., Viln-Lus, LithuPn-;.,)
Mcnthly Indcx of East European Accessions (ELAI) 1,C. vol. 7, no. 2,
February 19-18.

USPANOV, K.
Developing of grair, drying possibilities in the Virgin Territor-y,
Kazakhstan. Muk,elev. prom. 30 no-3.7-11 Mr 164. (NIRA 17:4)
1. Nachallnik krayevogo upravleniya TSelinkhleboprodukt.

7 1 ~ . ( ; . ,
F 7-, -, - -, - -,
- LYSRIIXO, J.Z.; X" DI, I.M.; DZHLKMAYEV. A.N.; USpAN6V, K.ye.
- ~- . -
Developing BYstems of forced pillar cave ~~in ~wori"ing fla d
ore daposits. Trudy Inst. gor. dela AR razakh. SSR 1:3-15 156.
(mining engineering) (KIRA 1~:I)

V5 rA A-,~c v, K. ~ j[-,
DZHAKMAYEV, A.N.; USPANOV, K.Ye.
fia
Analysin of basic factors affecting labor productivity of miners
in the system of forced block caving in leninogorsk Combine mines.
Trudy Inst. gor. dela AN Kazakh. SSR 2:44-59 157. (MIRA 10r12)
(Kazakhstan--Mining engineering)

WHAUMAYWO A.11., k-andidat takhnicheekildi nauk; K=11, I.M., kafididat tekhni-
cheskikh nauk; IUKOV* V.Aae gornyy inzhenexi.,
~#x I.Ye.
gornyy
,W
inzhener.
Block caving system of mining with use of horizontal boreholes. Gor.
xhur. a6.5:43-45 My 157. (RLRA INO
(Kining engineering)

DZHAKUPBAYF.V, A.N.; ISAKM, V.A.; USPANOV, K.Ye.
System of induced block caving in Leninogorak UdIbins mines.
Izv. AN Kazakh. SSR. Sar. gor. dela, no.108-42 158,
(MM 16:5)
(Ianinogoral: Region CEaut Kazakhstan Province) -,Mining engineering)

DZHAKUPBAYEV, A.11.; USPANOV, K.Ye.
Time facVq'i~ in connection with secondary spontaneous desintegrati*n
of broken dovn ore in sublevel caving s7stems. Izv. AN Xazakh. SSE.
Ser. gor. dela no.1:10-12 '59- (IIIRA 12:9)
(Mining engineering)

USPANOV, K.Te.
Pmalysis of horizontal block sizes In forced blocir caving
systems in mine 'a of the Loninogorsk Combine. Izv.AH Kazakh.
SSR. Ser.gor.dela no.2:1-8 '59- (14IRA 13:4)
(Leninogorak--~iniug engineering)
i

USPANCVg K.Ye.; ISAKOVI V.A.; MALICHENKO, Yu.I.; ALBOROV,. Z.B.;
HA 01, N.G.; KUTUZOV, D.S.
Systems of mining thin and medium thickness sections of the
Sokollnoye deposit. Trudy Inst. gor. dela ANkazakh. SSR
7:38-48 160. (MIRA 14:6)
(Leninogorsk region(East Kazakhstan Province)--Mining engineering)
0

DZHAKUPBAYEV, A.N.;. USFAj[QY,-4Jx.; HARLYBAYE.V, G.A.; PARNIKOV, V.P.;
DZHANSUGUROV, S.I.
Gonstruction parameters of chambers and pillars in a system with
complete filling in the Tekeli Mine. Trudy Inst. gor dela
AN Dzakh. SSR 11:3-15 163, iMIRA 16:8)
(Tekeli region (Kazakhatan)-Mining engineering)

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I r ;3 /Agriculture - redology Sep 49
"Activity of the Institute of Pedology, Academy
of Sciences Kazakh SSR," U. U. Uspanov, 3 3/4 Pp
Opochvo-vedlo No 9
MW Institute has carried out extensi-ve pedolo-
gloal-studles in Central Kazakhstan ana Dzhazkaz-
gin and. aided in founding an experimental stk~on
In the latter. Boll maps of Kazakhstan in various
scaloe ba-ve beou-completed. Data collected on Syr
Darlya, River have been of great aid to kolkhozes.
T2w Sector of Soil C-enesis is acti-ve in studying
Boil formation. The imutute has lacked close
1/50T.r,-
UM/Agricultwe - ..Ndology (Contd) Sep 49
connection v1th Party needs, but Is studying
memo to fulfill the Stalin Plan for the Trans-
fonwtion of Nature.
1/50T5

U L -1 "','.;j.
Usr.anov, IJ.U. "The land resources Of '-'IEO~erri K'azarklistan" (Froci fl :a--~er
given at the 4t!,i (Garlyev) se:~s;-= c~f t*-- Aca-3e.-:-, of cf "*,-,;-."~
1,
Vestnik A~ad. nauk Kazakh. SZR, ':c. 2~ ,. /':---77.
SO: U-3261, 10 j'.pril 53 (Letof is I z1hurn-al I nykli Statcy No. 12, 11)1,())

USE"Ovy ufuf
28M 0 Doyatellacati Instlute Pochvoyod Fasya An laz SSR. Pochwavedonle, ICA9,
so, 9 S. %"3
~~Sft. Lotopial Zhmmall nykh Statay, Val. 39, gmkwa, 1949

USPAY01i
M/Agriculture Soil studY
card 'A i Pub. 123 - 4/17
Authors I Uspanov, U., Dir. of Inst. of Soil Study
Title Basic results and the mos#" pressing taske in the study of the soil of
Ka-nakhetan
.Periodical t Veat. AN Kaz. SSR 11/1, 4.2-53, Jan 195L
Abstract I Sonte account is given of -,he preparaticn, of soil maps of Kazakhstan
and attempts to adapt the soil to the raising of grain and the plant-
ing: of trees.
Institution
Submitted