SCIENTIFIC ABSTRACT MIKHEYEVA, L. F. - MIKHEYEVA, T. G.

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• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001134120010-8
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: June 14, 2000
• Sequence Number: 10
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

r~t H.
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FELIDMAN, I.Kh.; -gy!TYEV -1J-;
BRBER, A.V. A, -Prinimali uchastiye-: BOCNOVA, V.P.;
Amino sulftdas and amino sulfonos. Fart 25: Addition of
p-acetoiminophenylsulrinio.acid to certain aldehydes. Zhur.-
ob.khim. 32 no.4:1046-16*) Ap 162. (KIRA 15:4)
1. Laningradakif khimiko-farmateevticheskiy institut.
(Benzenesulfinic acid) (Aldehydes)

6
_Ad utulwilp-
inartz. 1. VACMel" L' V, mWiceva, "a r. s. wiT
C1t*h1A(hf. V. Lomono&uv !state Univ.. NtaqN,W). Nphtal.
Sp~fti,&J UltChOd for the (Imint- dZy'!;;
Infers5ity of the rnf2!. kaybe;gh light smuErftiff in qmr-x
crystals it. the temp. rariv betwev, rmu tesnp. d fj
ar 00
The inethod was furtfirr drvelopcd fijr ail C431tv" of am
__it*1lS* gROW4" Arit 3?31f= awyalix the-
tUfthe
tnul. flucttuttion of tile dickc. pumeability of apAirtz is
much intensified mrith ;Vps~*Ch to thi.4 lslseri~n tellip.
I'lie plievainencit of a rcvfrvh'-~ 11-1. upalr3ccuce in a cryst.
gyhtttuiu tile range k3f pelynturpisit: WversionrL %v-.tsdiseovtrl:d
und tituutitatively nieamirEA. Ihsed um tlie-.e expu. tile
in th,
(C.'I. 22, "Itriji), 1119 intellso I tit tile rcatIptril light 11 pro-
[110fillull t,, A' TI'v -il ,f quartz Is hete de-
fil)'A a5 ,tic uf Ow ',!n,l ll,"F- br-l"r "I lt~ %Cry brisail
vfjj. 'eflef t and ilive"fou Cott"lly, 11i'l lucil'urm"C"Es were Ala
made with Li scpavilr dun- ,f (lie jufarized jxirtion3 I., ..
1. in tile 3-dimm-,ionjl codrdimlte5 of tile C.135"al
-
i
"
vatcl) with the I-.
axii iLltl,er (terixild
cul4r, or purallti t
.
16 tile iovich-jit light Ileum),
7he d"brizati6n a
]./I. increav--s ivith tile lemp. atul Isis a shurp discmlints-
ty III tile illvvrSirill rallgr'. T1". "t"'trositic" light tic-itter-
1119 W-.J!l mlly 0 3 Y 1,D-. 'I it ain atilt. of tit, A-sImpt-d
ITUA . Will ol"ll'--ruct
enon is viAble and -.vai
'
file lowEr tile lintilWA U11111. gradient in file crysital tile
mute highly dipen't'l a pmts %he ,palv~rrncr zme. TI;V
F
fly6cif pilettijult-slou of I
. Which IP(-&UA att Ili-
terise Inci'C'Ise 11) 111(J. flucEsultion lj'.~pquj Ole voillull silite,

with--i svith Ilse inUriv;t: ill cmuprva~iljfflty, nj ab u t
e
I A thi'. r 1)

-00189 V Mad. N40 1U1 .50vw
Phyf. "Dokwy" 1, 2m-miomWlinxi.
An exod.-study was nwdc of Q t dep-dence of-the
qUAr12 ill 4 ft0p.-
ty of
RnEwof Which Occurs tW
tange from M to W, Vrigh a Y11
Aha 0%ptr,, *0 In(Vals beapt,
dJ#rft1k_d A QiWAA AIL-
"101-4 ~Itl
cl Uarts 1"40"M tei-
the -401-
adkot, tat did wt mm. Ibc
=41 -dient t, 0. dimtiiju of dU4 L;~ of bom,
11 If
~4 light,was 0.03*/mnf. The cipt. required mote thv,4 72

ji
i. 7: Jim- - Neir the ra"Ol!tlOolat dw tcM0. thAnsed st

WO 7-fom Mal .
Above
!A rate Of WIFLIMal

-
,
.
Antensity ul's4mttakag of Jigbt corresponding to tmnsitl=4
'
-emcd for the first time, -, Also
when (me of,
Ito snild was uh
'
4
the t=i.
.
j the f aceslof thc
(f=rtz monocrystal had

of Int'l
i t1on temp., an optkally. htlet4aca
l
y
.
entl
omtteriap light developed Quatsamplewof i"JI, d
t WLwh"acrem. X-Mypbotosmphsl
Clad" S. M"T

PRiKirr'KO F
24(7)
~ 3 PUSS I BOOK KXPLOITATIOM SOV/136,3
V"~Tuz%vl' s'"404cftanl7l PO APektrosxoptl. t. ij
molakulYarnaya speict.~,mk-.plya (Papers of the 10th All-Union
Conferame on Spectriaca;rj. Vol. Ii Molecular Spectroscopy)
(L'Yov) lzd-vo Llvova'k.go inly-t%, 195T. 499 p. 4 000 copies
1. 1 c
printed. (Sor!ts, .4 Pity hrWy ebirnyk, vyp.
Additional Sponsoring Agsji~.ri kkademlys nauk SSSR. Koulaslya p0
op*ktrookopil. FA.i Jazer, S.L.) T*ch. Zd.z Saranyuk. T.V.;
Ultortal Mar4i "n4sterg 0.3 *;, A094emlcian (Resp. Ed., Dooeam*d).
Reporent, B.S., Doctor of ky.le and Mathematical ScIonc*e,
Fabelinakly, I.L. Doctor or Physical and KatherAtloal Sciences,
PAUrikant. V.A.. 600tor of Physical and Nathenatlo&I Sciences.
Koraltakly, V.0., c4Midat4 of Technical Sciences R4744y. 3.A.,
C&Wldat4 of "ioal $M Math4x&tlaal 341onces, kIlmovokly L.K.
Cand14ste of Phtolloal and Kattsmatical Salomon, MlliyanchU, T.S:,
C4Midat* of "Ij4l md Ka.UrAtLaal Salome* wW Glamboruan.
A. Y*., Candldat4 of Physioal and kath*~tlcaj lolenams.
CU'd 1/30
Usitse, M.P. Sp*ntr.pXotja%trlo Study of tam
Dispersion wW Xboorptim.1 of Sollas 97
todlovahenko, R.I., Lml M.N. 3ualwunsidy. Use of
Z1*0tronij C~ar_-tsrs fo- vtA Caljula~lon of
PrequoncLes of M-loo~dar Vil~rfttt~,;* 99
Petraah. 0.0., 3.0. Raut-'an. A4-sara4y of the
messureeant Of OptI32a penalty 102
Rautlan. S.O., 0.0. Petrash. A-)ouracy in Measuring
the Narrow libsorp'lin Lim@ WILIle Zzoludina the
Apparatus ftnGtIO!1 107
7411chkirA, T.3., L.P. ML&~yeiva' A. Yakwlev.
Molecular Vlvp671braff-Gr_L1VTT-DurIv4 nia" Troam-
Comatlone in Solids III
GlAsburg, V.L. ScatloriP4 of Light Near the Pheso-
-transition PoInto 115
30

FELIDMAN, I.Kh.; MIKHErEVA, L.F.; Prinimala uchastiye GORYNINA, R.M.
Amino sulfides and amin4'q4~-fones. Part 291 Reaction of
p-acetaminaphanyl hydroxymethyl stilfone with amines. Zhur.ob.khim.
33 no.7:2116-2119 JI '63. (KRA 16:9)
1. lAningradakiy khimiko~farmatsevticheskiy Inatitut.
(Acetanilide) (Amines)

M I KHEYEVA, L.F. ; I i ~4, C f ,
--' IF~-~-P]Qcn cf -rt, pri.irriviton pinne in quartz nea: *rl.
temperfit;rt -1'cl phase tranoition. Kriatailograf,.q 9
nr, . " :4~ .~-41 - ~'Z-y f I . ~t' I . - . -
1 . Moskov 0- " y a r~: !, V,-I'llyy Uri; ; P. ~, ~ '-~ * . TP, - P, *, ~ . - zf,l, -,,~ , -

141KHEYEVA, L.F.
Anotylone durivativen. Reaction ()f nonf=jkgnfjslujn b-ra,(-brrjty,rInp
and dimagneolum dibromoacetylone with A-dikotones. Zhijr. org.
khim. 1 no.9tl536-1539 IS 165. (ICU 18: 12)
10 Leningradakiy khimiko-farriiatofivtlclier~kiy 1-m-3titut. SibrLitted
March 24, 1964.

HDUM,MAj L. I.
KIIUIEM, A, L. I. wMe globinAeme coerficient under nomal corklitions
and in certain blood dineases." Min Health RSFSR.
Moscow MedicAl Stomatological Inst. Moscow, 1956.
(Dissertation for the Degree of Candidate inASciences)
Med ical
So: Knizhnaya Letopis', No. 18, 1956

SH&MUN, A.M.; MIKKKUVA, L.I. - MIKOIAUVA, N.V.; SLOVORHOTHOVA. 1.A.;
Baux, 0. ." 0 H.; STUPYIEDVA, G.A.; GUSUDYA. I.A.;
(;M6Jfo'KhTA. V.V.-, VOLCM9K. K.Te.; JKIRUWA. V.S.; PAJOIA, Y.T.;
KIMSONSIDLYA. IF. M. -,
Connection between enamel, the dentine, and the organium an a
whole. Vrach.delo no.2:203--205 F 159. (M IM 12: 6)
1. gufedru biokhimit (zav. - prof.A.E.Shftrpenak) Moskovakogo
meditsinskogo stomatoloecheekogo inntituta.
(7F.91M)

KKIEYEVA-,
Globin/heme coefficiernt, globin capacity of er7throcytes, &ad globin
index in varlouB hematological diseases. Probl. gemat. I perel.
kravi 5 no.2:19-20 F 160. MA 1415)
1. In k&f#Aj-y blokIdmil (oAv. - pnof.
meditsinskogo stmatologicheskogo instituta (dir. - dotsent G.N.
Beletskiy).
(HEMOGLOBIN) (BLOOD-DISUS:Z)

DOGELI , W.V., kand.med.nauk; jgXk kand.red.nauk
Indices of medietors of the bl:~od in brcnchial astl=a in
children and their change under the infl,-,ence of ccrtliscme
therapy. Pedlatlriia no.9143-47 (XIFLA 14:0
1. Iz klinicheskogo otdela (zav. - dotsent F.P. Savatimsi-ava)
Instituta diatrii Moskvy (dir. - dektor ned.raU A.P.
Chemikovar.
(ASTINA) (CORTISONE) (ADRM:AL114-B) (CHOLD-ESTM~-SE)

nWNR',1 AT5003221 S/2563/64/000/237/0021
/0025
THCR:: -Dmitrevskiy,-V. A.- Mikheyeva, L.- 1.
A
L
TITIZ: Desi~nin~g reciprocating engines for nonrated operations
SOURCE: Le ningrad. Politekhnicheskiy institut, Trudy, noo 2-37, 1964-
1--Tepl(jvyye mashiny4-dvigateli vnutrennego agoraniya i transportnyye mashiny (Heat
enginea;Internal combustion engines.and transport machines), 21-25
TOPIC TAGS; ::rediprocating engine, self regulating engine, outlet pressure,
6iesql compressor, external dead centert indicator diagram, operational zone,
curve
po f -rop
ABSTUCT.- The design of -reciprocating enginC3 caLls-for a determination of their
particular operational zone. The performance of such machines is determined by
the changes In the following two parameters: the fuel feed and the pressure at
the. compressor outlet. A change in these two magnitudes changes all the other
diesel and compressor parameters, and themachine automatically changes to a
different operational routine, The machine cannot possibly function beyond the
boundatlea of Ltd operatiohal zone because a),the piston may strike against the,
cover and b) the air compression within the engine cylinder will be inadequate.
Card 1/2

USSR/ Physical Chemistry - Therrzdynandcs. Thermchemistry. B-8
Equilibritua. Physicochemical Analysis. Phase Transitions.
Abs Jour Referat Zhur - Khirdya, NO 3, 1957, 7486
Author M hbAmpya, L.M... Novoselova, AN., and Biktimirov, R.
Title Determination of the Solubility of Calcium Fluoride and
Calcium Beryllium Fluoride in Water and in Hydrochloric
Acid Solutions with Tagged Atoms
Orig Pub Zh. neorgan. khimii, 1956, V01 Ii No 3P 499-505
Abstract The solubility of CaF2 in water and in 0.001, O.Oll 0.1,
and 1N HC1 at room tenperature increases from OoOO0205
Mles/liter at PH 'r to 0.0363 Wles/liter at PH 0-3-
Saturation os attained after 20-40 hours. The solubili-
ty of CaBeF4 was determined at HC1 concentrations of 0.01,
0.1, and IN; as in the previous case the solubility was
found to increase with adidity from 0.00093 mle/liter
at PH 7 to 0.0974 moles/lIter at PH 0.3. Saturation was
reached after 50-300 hours. The solubility of CaBeF4
Card 1/2 - log -
Card 2/2 - 110 -

IA
LA I
I UT, n n i

in o! in - 4. r
I
j r
r. i v-7,
ri t j r I
r i n r.
-i -ri n i f r i i w r. p
~i

3n thc.- Probiem of thr. ir ~4,jcti ,n of Li thium-Bem'', : 1 urn i I- P, - ,- - ~ 'A ~
FiucrliE Fron Aqueous -cLuli6nq
K'.TT'n : jaly -1, 1957
Card 3/5

MIKHEM,VAI_L.M-G; MIKHEYEV, N.B.; PCHELINTSEVA, G.M., red.; TARAKANOVA,
A.A., red.; VLASMA, N.A., tekhn, red*
[Radioactive isotopes in analytical chemistry) RadloaktivMye
izotopy v analiticheskoi khimii. Mosk7a, Gos.izd-vo lit-ry v
oblasti atomnoi nauki i tekhn., 1961. 98 p. (VIRA 15:1)
(Radloitiotopes) (Chemistry, Analytical)

HIMEYEV, N.B.; M1101EYEVA, L.M2 - -
Effect of complex formation on the separation of elements by
cocrystallization. Dokl. AN SSSR W no.5:1109-1112 L 161.
(MIRA 14:12)
1. Institut fizicheskoy khimii All SSSR. Predstavleno akademikom
V.I. Spitsynym.
(complex compounds) (Crystallization)

HIKMEVs N.B.; KIKHEYEWA, L.H.
Effect of complex formation on the cocrystallization coefficient.
Zbur.neorg.kbJ- 7 no.3s671-675 Mr 162. (MIRA 15-3)
(Complex-compounda) (Crystallization)

nnamyu, N.B.; MIMEYEVA, L.14.; MALININ, A.B.1 MONO,, M.D.
Pffect of' corplex formation on the separation of elmento
during cocryatallization proceeding in accordance with the
logarithnic law. Zhur.neorg.khin. 7 no.9-.2267-2270 S 162.
(11',IRA 15:9)
(Complex compounds) (Crystallization)

33 76 2
5 5 60
S/075/62/01 7,~00'!003,'003
B106 'B101
AUTHORS: Mikheyeva, L. M,, and Vikhitill, I
TITLE~ Determination of arsenic, phosphorus, and su'fur 1,n
beryllium oxide by radloactivation analysis
PERIODICAL: Zhurnal analiticheskoy khimii, v. 17, no 1, '962. 94-a6
TEXT- Bv the method of radioactivation analvsis. !0- 4-. 0-2 % of ars*~n
phosphorus, and sulfur were determined in a beryllium oxide preparati on
containing no other elements The samples were irradiated wi th neutrons
in the nuclear reactor of the Central Institute of Nuclear Erq-ineering
~2 3,) 76
"Eastern Germany) The radioisotopes P S and As were formed diring
t!-,p a-",vating irradiation In the sulfur activation, the reacton
3 (n,P)P 52 proceeds as side reaction which may elevate the resu 'ts of
phDsphor-us determination This error could, however, be neglected since
experiments showed that it was within the error limits of de-krminations
OwiRg to the small capture cross section of' Be for neutrons it w4a ri-t
tc make a correctl,~,n for the Belf-absorption of neutrDns -,n th~
Carl 1. 1

46
3 -'7b2
S/07 5/62/0 17/00 ', ~00 1, 00
Determination of arsenic, phosphorus... B-06/B101
3 am~ 1. e The substance to be analyzed was beryLlium hyd-,3xide -~,nverte!
t(, oxide by 4-6 lira ca~,~Ination at 12000C. Dur-,ng callcina-cr. -.n Fiat',n~m
:ri-.1b-es -inler such conditions, the beryllium oxide w~is contaminated Ir"h
a: C ,It ~) - 1-2 ~Lg of Iridium per I ~ of beryllium oxide Therefore, thr-
samptes were calcined in quartz zrucibles, Three samples overe ',rrad:at~-Ii
in each determination, the prepiIration to be analyzed and tw:, standards
with the beryllium oxide to be analyzed as a basis and addit'cns of 0 0' Y,
-r 0.1 % respectiv-1y, of the eiement to be determined 'hk samples wer;-
dried at *100C before activation During activatlen f'O hrs 'rradiatlcr
*3 21 1.
-vith a n-utron stream of a density of - '0 neutrons cm i8o.,C) th&~ sampl-l
mAre plazc-d in sealel jupirtz ampuls About ~O hrs after t,e '.rradiatior,
tric! pr,-pparalions were worked up Each element was det,~rmlnqd from a
banple Ar5rtric was pre~ipltated as 3-;'.fide. prIsphc-,.3 as
and salfur ag bariam sulfate Ph:- BT s
i~-' taled with arsenic suifid,~- Therefore. th,~ a-tlv~-,v f a-
:.fld-a was measured in the pres-:-? If an a-~Jnn~,r.
'~* -'~6 rg/',m2tti-knoss which abscrbf~d
Carl 4 t

33762
S/075/62,'0'7,'G0', "~;' 30~
Determination of arsenic phosphorus. B'06/B~O'
9 9 1% The arsenic content of the beryllium oxide sam;-.e was -al-ulate~"'
2- 1.) (x - percent amount of th,? e'ement - b,~
from the formula x - al,/(I
determined; a = amount of the element to be determined. added to tr"
standard sample (In %, referred to beryllium oxide)l 1., 1 2 ' rai;c-
a::tivIt,es of the element to be determined in the sample and in the
standard) Deviations from the mean value of values salculated by the tw
,3tandards -Aere below 3 ~t for the arsenic determination. For the P deter-
ammonium hydrophosphate served as a carrler The determination
was performed after separating As as a sulfide. In this case, the
deviation of the two values from the mean value did not exceed -' 4 S
was determned without previous separation of As or P. Ammonium aulfate
serv-d as a carrier The barium sulfate precipitates contained some
phosphor-us Therefore, the 3 activity was determined by analyzing the
curves for the absorption of P-radiation by aluminum filters Deviations
from the mean value were 1 6.2~ lo. The error of determination of smal.'
As, P. and 5 amounts by radioactivation analy3is is of the same order as "r,
determinations by Instrumental analysis methods The rad,.cactivation
ana,yqis is 1e93 cz7iplicated which is particularly valuable for singl-
Card 3/41

33762
E/'0'5/'62/'O"7/ 00'.or,,,, 1: 0
DeterminFi*ion of arsenic, phosphorus B106/BiOl
det~rmlnations Besides, the element to be determined need not be
--Wnp-etely separated from radioactive impurities (caused by foreign
raj~~-Dtopes) There are ' table and 7 references: ~ Soviet and
~ T-.~n-Sovl~et The referen,-e tc the English-langua~e publication reads
as follows: Smales A A , Atomics A, 5~ (1953)
ASSOCIATION: Moskovskiy gosudarstvennyy universitet im M V Lomonosova
(Moscow state University imeni. M. V Lomonosov) School of
Higher Technical Education, Dresden (Eastern Germany)
SUBMITTED- Desember 16 1960
C a rd 4 /4

L 1960645 W(M)/EWP(t)/rY1P(b) UP (a) ISS61AS (r4p) -2/AFMDC/AWAFPM/-
!~ ~D") ...... .... b/4G
ACCESSION MR: AP5003151 s/oo2o/61f/l58/002/0(#40/(YAl
AUTHOR.' :14ikheyev- A*- B.-. Mikheyeva, L. M.;
TITU;.- :-Hectiiwiejw,of.coprecipitation of microquaintities of Xttrium with,hydroxides,_
of 1xilyvale"t metals ""7
1: SOURIE: AN'SSSR. v. 158, no..21 19~4j 44o-441
TOPIC TAOS:',yttrium, ir-on,-zirconium isotope, electrostatics, ion exchange,
4dsorptionj~'slkali, che/Mical separation, radioactive source
ABSTRACT.
~ABI
:The. mechan ism of the coprecipitation of oLcroquantities of.radio-
4c
active Lsotopes.wLth hydroxides of polyvalent. metals depends both an the
pr,
propertias~o'f the hydroxides and on the state of the microelement in
'go
solution. nW iouthors proceed from the hypothesis that in the region of
ac
acidity of the 6441um when yttrium exists in the Ionic state, Its coprecipL-
'I
.tation with hydrosides of polyvalent m 81%. FOCOR)3, 2:r(011)47 should
yd!talsa/
ocCu on accodat of electrostatic ph Cal irsorptLon. The caprecipitatLon
of -YWwfthout~-a carrier with
of. Pe(OH)3 and.Zr(OH)4-as afunction of thl
C&M 1/2,
Ca;

KORYAKIN, V.I.,, kand. tekbne nauk; DOROGUTDI, B.S.; CHISTOV, I.F.;
CHERUANOVAp I.V.; DAVYDOVA, M.I.; SOROK01MWA, R.I.;
XIKHEr3VAq L.V.;OWAGEr, V.G.; VOIXGVAv L.H.; SUMARZEDIt V.P.,
k8W,tek1M. naukp red.; KUZIIZTS(N, G.A., red.; ZAYTSEVA, L.A.,
takhn, red,
(Technology of the production of wood chmdcals; a mfumal for
foremen,, technicians, and engineers] Tekbnologiia proizvod-
9tva loookhimicheakikh produktov; posoble dlia masterov i In-
zhnerno-tekbnicbeskikh rabotnikov. Moskya# Goo.izd-vo meet-
noi prouqshl. i khidozh. promyslov RSFSR, 1961. 383 P.
(MIRA 15:3)
.(Wood--Cbemistry)

MTKIIL-YrVAP :4. 1.
36875. C diagnosticheskom macheiiii lzmenf~niy s( storony pochek pr'.
rets"cliviruyushchem enciokardite. Trudy Med. in-ta (Izhov. go3. med. in-t),
t. ix, 1949, c. 156-6Q
SO: Letopis' Zhurnnl Nykh itqtey, Vol. 50, '-Tos~va, 1949

ic~iSKAYA, B.D., doktor maditainakikh nauk; GUJSIKOYA, H.A.; HIKHMU.14.1.
Some factors indicating renal function and chloride metabolism
during systematic intake of Unvo-1zhevsk mineral water. Urologiia
22 no.6:50-54 U-1) '57. (KIRA 11:2)
1. Is propedevtichenkoy torapevticheskoy kliniki (zav. prof. A.Ts.,
Gubargrlts) Izhevskogo meditainskogo Instituto.
(KIDIW FUNCTION UUTS, off. of drugs on
mineral water from Uovoizhavsk)
(CHWRIDES, mateb.
off. of Novoishovsk mineral water)
(MINIMAL WATM. off.
Novoithevsk mineral water, on renal funct,
on chloride metab.)

PjWZy3KI'Y, V.N.; Prin,in ~ I I uo~,-- . .;'(,,'/A, *-I. L.; ~ it .::. ;
VUjTSik;ifGlfL;K, A.K,
G h~,-mi cal -Ly ,; -,, , *-)).,,, pki if, , - 1, ~ ~ i n ~ 3 f :' t .,, , ! C-: :1. 1-, ' - -.1 ~ 41 ~ IWI
alioys ~ n t. i -- pr~,c -- s , of contour in,!-nsLonkl Lnkokras.
mat. i ikii prim. n,;-.3:37-il '63. (:iI?A 1():))
(Pro,,ective co:itin.-s)

SUBJECT USSR / PHYSICS CARD 1 / 2 PA - 1847
AUTHOR ALEKSEEVSKIJ,N.E., MICHEEVA,M.N.
TITLE he Critical Amperages in Supraconduotive Tin Films.
PERIODICAL Elrn.eksp.i teor.fis,31, fasc.6, 951-954 (1956)
Issued; 1 / 1957
Planev disk-shaped films were investigated. The current was led in vertical
to the disk and collected at its periphery; in this case H - 2I/r holds for
the magnetic field on the surface of the disk. Here r denotes the distance
from the center of the disk to the place were field strength is to be
measured. The tin film was steamed on under a diffusion pump in a high vacuum
at the temperature of liquid nitrogen. Special supraconductive leads were
used, and the pulse method was employed for measuringl besides, the film was
in immediate contact with liquid helium.
The current pulses allowed to pass through the sample were produced by a source
connected in series. The current- and voltage pulses were registered by a
loop-oacillograph. The experimental system was fed by a 220 V-1aboratory
battery. By the variation of the parameters of th a stem it was possible to
obtain pulses of different duration (usually O'l :Z and amplitude. It may
be seen from &a attached oscillogram that the voltage pulse occurs at a certain
intensity of the current passing through the sample. This is the critical
amperage for the given experimental conditions. The linear dependence Ik(r)
obtained is indicative of a nearly radial distribution of amperage and of a
weak influence exercised by the heating (during the current pulse) of that

ALEKSEYEVSKIY, N.Ye.; MIKHEYEVA, M.N.
Critical currents of superconducting tin films. Zhur. eksp. i teor.
fiz. 38 no.1:292-293 Jan 160. (MIRA 14:9)
1. Institut fizicheskikh problem AN SSSR.
(SkVerconductivity) (Magnetic fields)
(Tin--Electric properties)
ARKHAROV, V.I.; EBLENKOVA, H.M.; MIKHEYEVA, M.N.; MOISEIZV, A.I.;
POLIKARPOVA, I.P.
Change of magnetic misceptibility and the behavior of small impurities
in the decomposition of an Ag - Cii solid solution. Izv. AN SSM.
Ser. fiz. 28 to.1:146.151 Ja 164. NIRA 17- 1)
1. Inatitut fizlki metalloy AN SSSR.

ACC NR. AP7006124 SOURCE CODE: UR/0056/67!052/001/0040/0041
AUTHOR: Alsksayevokly, N. Ye.1 M~~ ~"&. M. N..
ORG: none
JITLE: The superconducting properties of aluminum films
SOURCE: Zhurnal eksperimental'noy I teoreticheskoy fiziki, v. 52, no. 1, 1967, 40-41
TOPIC TAGS: aluminum, aluminum film, ouperconductivityo 04q"W4""~ -
~
#hTc.t4l i -IN! ~M . Ip A PfrrybIME49A_ rIA-M 0 CX1 r.1 C,9,L POO A) f
ABSTRACT: The superconducting properties of thin aluminum films, obtained by
vaporization and condensation In a 10-6_10-7 mm Hg vacuum at liquid nitrogen tem-
perature and annealed to room temperature, have been investigated. It was found
that the critical temperature Increases with decreased film thickness. For instance,
the critical_temperature of a film, 8.9110-6 cm thick. was 1628'K, while that of a
film, 7.9-10 6 cm thick, was 1904'K. It is concluded that, since the experiment was
conducted In vacuum, the high critical temperatures of thin aluminum films were not
the result of the formation of oxide layers on their surfaces. [TDJ-
SUB OODE:11120 SUBM DATE: none
Card

BAI-S , Yt,, A. , KO'-,U~ , -7.3. : :-'I ~'~ ;,"- . . 1: . i .
Ra ' 'A -) c f -, r. - v- -, "t , . ~ . - -11 ~ ! :. ~ L *. I t~ * . , ~ - F . I , '- - ~- !
i esen-o 4 r 4Pi*,-r,4 f' : - I - - 1 A s . Ne f ' -3 p, a z , g, - -'- , i - I- ~ 7, - . - ).
(y,
,'. " - 51 '64 ... T .ball -1 . )
i . In t i tut gf, ,I ~', i i r itx tk.L 1:, r -,ru i. . !7 r - pi ',;
SSSR. . .

OT. X.S.; HIMMYVA, N.Y.; MAMMA. 0.A.
Haterocyallo compounds. Roport Yo.41, Synthetic anesthetics. PkLrt
Xatere of 1.2.5-trimethyl-l~-ar7l-di.-piparidole. rtnr. ob. khia. 26
no.10:2820-2834 0 156. (KM 11:1)
1. Moskavokly Institut tonkoy khimichnskoy tekhnologii imeni H.To
Lanonosova.
(%store) (Piparidins)

HAZAROV, I,No; PROWAKOVO H.S.; HIMTJIVA. U.N.; SHATRYGINA. O.A.
Heterocyclic compounds. Report No.40: Synthetic anesthetics. Part 5:
Motors of 1,2.5-trimthvl-4-phenvl-li.-piparidoI with aromatic acids.
Shur. ob, khIm. 26 no.10:2812-2820 0 156. (MIRA 110)
1, Nookovskly inatitut tonkoy khimichookoy tekhnologit imeni N.V.
Innonomova.
(Motors) (Piperldine)

Ile r-),3yrl i c -.,~ . T, * , P. -. .. . I
'? " t
et':.er is i f r
cynt..eoi zed ',y
4-Pi~er "don t
i r te r -.~ o r c -:a, r, i!-~. -,t
-4-pi
of ir,~ i -,ni- e
ily 1-,~
C. 1. 1,
ef 'L - - Ac - - r
~~-o f e j ... v ;,)y
t i
C:~ t -t: r t - t
t', e propi or~ at e d 0 .3.i'. t i-,e iZ.,
s t r -, r. g e r~ nalL~eoic
i t i t
tolzi ---,ty. ",717 L-

c C 0 0 7- 0 Z . S
o'- ir e---- -2
in ve s t 4. -L- t ion o 11 e pu'-- I so :ar-- C, -
experime- t al lj,-:,t f o
of whic!. P-rc? Scv; Ot .
I-.: lllockovc,;~iy ir ~A -4 t -it
ld.V. Lomonooova (.,loscovi In 5~ t
TechnoloGy imeni ~:.V.Lomono ov n
khi:-.ii (Chair of 3r--aric C,
Octo'--er 4,

79-20- 4-26/60
AUTHORSi Nazarov, I. N. (Deceased), Prostakov, ". S., ZjkL~~ ~. Y.
TITLEt Heterocyclic Compounds (Geterotsiklicheskiye soyedineniya~ 61.
Synthetic Anaesthetice (Sinteticheskiye obezbolivay-ushchiye
veshchestva) XXV. The Esters of tte 1,2,5-Trimethyl-4-Phenyl
(Aryl)-4-Piperidole (XXV. Slozhnyye efiry 1,2,5-trimetil-4-
-fenil (aril)-4-piperidola)
PERIODICALi Zhurnal Obshchey Khimii,1958,Vol.28,!Tr 4,pp.960-968 (USSR)
ABSTRACT: The authors investigated the influence of the structure of
the asters of the 1,2,5--trinethyl-4-phenyl-4-piperidole
on their physiological activity and have obtained a new
series of compounds of this type. The T-isomer of the
1 2,5-tgimethyl-4-phenyl-4-piperidole (melting point at
1;7-108 C) M, the propionic ester of which is a strong
analgesic (Ref 2) - at present It is frequently apilied
under the name of "Promedol" -, was etherified by acid
chloride.
Card 1/3

7') -20 -4-26, SC
Heterocyclic Compounds, 6!. Synthetic knaesthetics. XXV, The Ester-- *,I.e
1,2,5-Trimethyl-4 Phenyl (Axyl) 4-Piperidole
C 6fl, Oil C()H OCOR
11 H C I
3 RCOC1 3
CH
3
C 11 ti
R=n Cil30C 6R4OCH 2 ~Il); P=n-C 2R5Oc6 R4OCH2 (111); .9-C 6H5 OCHCf13kIv)
R-C H OC(CH ) (V)i R-n-C OC(Cil ) R-n
6 5 3 2 1 C6114 3 2 (V'); -?102C6'14()Cl'2
11-n-11112C6114OCH 2 (VI'')' R-(VkH(IX); R-C 6115--C --C (X);
R -oc- C 4H30 (oe.--furyl) (XI); R-C6if5 SCH2CH2 (XII).
According to pharmaceutical investigations carried out in the
Card 2/3 laboratory of M. D. Mashkovskiy some of the mentioned e3t,~rs

7~-2 9-4 -2
Heterocyclic Compounds. 61. Synthetic Anaeathetics. XXV. The Este~-s of the
1,2,5-Trimethyl-4-Phenyl (Aryl)-4-Piperidole
0~'TA'21011s
SUBMITTED:
have considerable locally anaesthetizing effect. The degree ~-.f
the anaesthetizing effect, which was determined according
to Renlye's method, is given in the table for 3ome of the
preparations. The complete results of the pharmaceutical in-
vestigation of the preparations obtained will be published
in a separate paper. There are 1 table and 4 references, 4
of which are Soviet.
M
onkovokiy institut tonkoy khimiohenkoy tokhnologii
O'loscow Institute for Fine Chemical Technology)
April 1, 1957
Card 3,13

NAZAROV. I.M. [deceased); PROSTAKOV. U.S.; NIKHMVA N N.
,
Naterocyclic compouads. Part 62: Stereoisonarlsim of 1-acyl-2,5-
dimthyl-4-piparidones. Zhmr.ob.khlm. 28 ao.9:2431-2440 S '58.
(KIRA 11:11)
1. Kookovskiy inatitut tonkoy khimicheskoy tekhnologit.
(Piparidons) (Isocarlem)

ikheye in., I i
TITLE: Heterocyclic Co-,I-jour "fi (Getcrot~-,Ikl i (-~,enkiye
6 ') . Sy:it.,etic A-enic-q (( 11 Si r,teti c~.csi: iju- -)- Q- ;vayushchl-
ye vesnc ertv a ) XXV I. ~-,reo In ,me r4 f 2,
4-Fhe~.yl -4-ei, er' d r) I a 1- 11 1 -A cyl -2 '-D. (,t y-4-
I i ipr _rlol r (XXV I. St4~rQAzo-crivR 21i-- I
pi .,eridol --v i I i 1 - 27-di 7,e ti 1 -Z -f 1 -.-pi
PERIODICAL: Zhurnall obni-x :.ey 1,himi i',Ij 9 Vol 2'3 Nr 1 o
pp 2746-27c7 (U~;SR)
ABSTRACT: The -:~..,thors coz-.tin,_;-_--d tneir investi,_-"tions in t.-, u r i -2
of t',-e 1-alkyl-2,5-di-let.-,'."-4-aryl-4-pi..er:J')~s rt.-A
t',eir esters (Ref 1) by synthesizing tne analo,-9 of t..eE,~e
piperidine alcohols with --n acy'. radical as su_-stit.e.-.t
on the nitrojer. Trey obtained 2,5-dimet-~--1-4-pl%
piperidols the trw.sition of w-ich to t-e ear''er deczr:-el,
-isomeric 1.2 95- -eriJ.-.s
stereo trimethy~-4-phenyl-4-pi'
(Ref 1) was successful. 2,5-dinethyl-4-p:,er-y'l-4-pi--er"~-:s
Card 1/4 (IT~ is formed by the reaction of pner,%,! lit:-.i~im wit%

Heterocyclic Compolu;(,'~i. 0.,'.Syr,t:-.etic Anal,xe~,-~C.11.
XXVI. Stereo
2,5-di7,etriyl-4-i.i,.er.,Iorlf1 (i
C C i 5 Li
H
5 H
H " I
I)C
U T
Of t e f ou r stere-)- ~-c-7,ors of t,.e
a r e t- -e-~ret"eL,11y ;possible tne 7- ani t~,e :,-1,7 ",:.er
separ-:--ed in crynt~illine for,~. Th-- th :~ I:,
this pi;eridol II) va:-, obt~,i:~ed in t:. :, r-7, of t
11-ac.-~t..-I leriv;Aive. T,,.c, septration -,f t e r~er-
pi;)e ri (I r) 11 wa F3 car ri o,i out cl.r,,) t -:- - - - . ' Y o,
oxi 11 o ~,y (, rys t i~ I I i ~-.a t i jr, . t:.c, a, t i
0 f ~ i , f- r I :1 1, C -,,- r ~ !- e di n t:-.e r t c:.
act i ~ cf' I r- --i,l le ard -i-
Card of t f, i r o f p i i~t- r i d o' into t.-.p

Heterocyclic Compounds. 6,7#3.ynthetic Analgesids. S0'1/79-28-'o-2"1j"6o
XXVI. Stereo Isomerism of 2,5-Dimettiyl-4-Phonyl-4-Piperidols and I-Acy,
'),5-Dimethyl-4-Phenyl-4-Piperidols
special interest. Thus the following compounds were
synthesized in yields of up to 85%: (VI) 1-acetyl-,
(VII)l-propibnyl -, (VIII) 1-benzo I-,(IX) 1-diethy!
aminoficetyl-,(X) 1-mesyl-, and (XI~ 1-benzene sulfo-2,5-
dimethyl-4-phenyl-4-Piperidol. Theoretical conclusions
were drawn from the results obtained. There are 5 refer-
ences, 2 of which are Soviet.
ASSOC IAT IOIT: Koskoyekty institut tonkoy khimicheskoy tekhnologii
(Moscow institute for Fine Chemical Technology)
SUBMITTED: October 25, 1957
Card 3/4

Heterocyclic Compounds. 63.Synthetic AnalgesicsA SOV/79-28-lo-25/'60
XXVI. Stereo Isomerism of 2,5-Dimethyl-4-Phenyl-4-Piperidole and I-A-yl-
2,5-Dimethyl-4-Phenyl-4-Piparidols
Card 4/4

MMEYEVA, N. R., Cand of Chem Sci - (diss) "Me Synthesis on the basis of V- Piparyis
of Physiologic&Uy Active Substances - Pipei-yl Derivatives (Anestthetic3, Analgesics,
Spasmolyaesp and Others)," Moscaw, 1959, 1.)j pp (Moscow In5titute of Fine Chomical
Technology im M. V. Lomonosov) (KL, c~~, 123)

HAZ"OV, I.N. [deceased]; FILOSIMOV, U.S.; N.V. ; DORUNIN, VA.
Synthesis of Schiff bases froo 1,2.5-trimetkWl-4-piparidone
and aromatic amines. Izv.vys.ucheb.zav.; khln.1 khIn.tekh. 2
no.5:726-729 '59. (KIYA 13-- 8)
1. Hookovokiy institut tonkoy khimicheakoy takhnologii imeal.
H.V.Lomonosovu, kafedra organicheskoy khimli.
(Schiff bases) (Piperidons) (Amines)

5 (3)
ATTHORS: flazarov, I. N., PrOst&KOv, ?'T- S-, ZOV/79-Z9-7-40/83
Mikheyeva, N. 71., Davydova, S. L.
TITLE: Synthetic Anodyne Compounds. Ir-Piperidones, r-Piperidols
and Their Ethers (Sinteticheskiye obezbolivVushchiye
veshohestva. V-Piperidony, r-piperidoly i ikh efirj)
PERIODICAL: Zkwnal obahchey khimii, 1959, Vol 29, Nr 7, pp 2285-2292 (USSR)
ABSTRACT: The authors continued their investigations on the synthesis of
r-piperidole and their ethers, the analogs of promedol and
isopromedol (Ref 1),and obtained a number of new ii-piperidones
by alkylation or acylation of the 2,5-dimethyl-4-piperidone
(Refs 2, 3). The 1- ~-pheayl ethyl-(I), 1- ?--phenyl allyl-(II),
1- A-p-nitro phenyl ethyl-(III), 1-phenyl carbo-metho3ty-aiethjl-
(IV), 1-(3',4',5'-trimethoxy benzoyl)-(v7i), 1-nicotinoyl-(VII),
1-furfuroyl-(VIII), 1-(1-diethyl-amino propionyl-(IX) and
1-carbo-benzoxy- 2,5-dimethyl-4-piperidone (X) were synthesized.
Compound (V) was obtained by the reduction of the nitro Irroup
of 1-p-nitro benzoyl-2,5-dimethyl-piperidone (Ref In the
case of hydrogenolysis of (X) the initial-2,5-dimethYl-4--
piperidone is formed. Synthesis of the r-piperidols was
Card 1/2 brought about by reaction of the corresponding iperidonea

I C)/fj 7
Synthetic Anodyne Compounds. 4-Piporidones, '1/79-29-7-4
r-Piperidolo and Their Ethers
with organolithium compounds or also by substitution of
hydroCen of the nocondary amino group of the 2,5-dimetiVI-4-
phenyl-4-piperidol (Hof 4) by the corresponding radic.alo. The
followi compounds are obtained: The piperidola (XI), (X]J),
(XIII)v 7XIV), (XV). In the case of other formation of piperidols
by means of acid chlorides the ethers (XVI), (XVIII), (XIX), (XX),
(XVII) the and 4--isomers of 1,2,5-trimet)1,(-1-4-phenyl-4-
piperidol (I), (M) and ()CXII) viere obtained. For th2
pharmacolojical test the hydrochlorides of the ethers of some
tertiary and secondary 1-piperidols were prepared (more exact
information in the experimental part). There are 4 Soviet
references.
ASSOCIATION: Moskovskiy institut tonkoy khimicheskoy tekhnolo.-ii
Inntitute for Fine Chemical Technology)
SUBMITTED: June 23, 1958
Card 2/2

~ (3)
A"THORS. Nazarov, 1. N., Prostakov, 9. S., SOV179-29-8
Mikheyeva, N. N., Kirilovioh, V. I.
............
TITLE: Synthesis of 1-Oxyalkyl-2,5-dimethyl Piperidines
PERIODICAL: Zhurnal obahchey khimii, 1959, Vol 29, Nr 8, pp 2508 - 29"~
(USSR)
ABSTRACT: For the synthesis of the amino alcohols which serve as inter-
mediates in the syntheses of the analgesic-, local anaesthetic-,
and spasmolytic pharmaceuticals (which contain a ring-subuti-
tuted piperidyl radical as an amine residue), the authors used
2,5-dimethyl-4-piperidone (I), which results, according to
I. N. Nazarov, from propenyl. iscpropenyl ketone and ammonia
(Refs 1,2). By reduction of hydrazone (II), according to K-W~iner,
compound (III) was obtained with a yield of 7W6 (Scheme 1). The
introduction of the alkoxy substituent into the nitrogen of the
piperidine ring was carried out in various ways: as in the di-
rect reaction of piperidine (III) with ethylene chlorohydrin,
compound (V) also resulted by reduction of the ethyl eater of
acid (IV) obtained from (III) and ethyl bromoacetate with lithi-
um aluminum hydride. The reduction of hydrazone (VI) of the
Card 112 1-0--hydroxyethyl-2,5-dimethyl-4-piperidone likewise lad to amino

Synthesis of 1-Oxyalkyl-2,5-dimethyl Piperidines SOV/79-29-e-"/5'
alcohol (V) (35% yield). The ethyl eaters a-(VII) and 0-(VIII)
of 2,5-dimethyl-piperidyl-1 propionic acids were obtained by
condensation of the eaters of the corresponding bromine-substi-
tuted propionic acids with (III). The methyl eaters (IX) ind
(X) were synthesized in the same way (Scheme). The amino ke-
tone (X) was also reduced by sodium to the amino alcohols (XI)
and (XII). The condensation of 2,5-dimethyl piperidine with
propylene oxide in an alcoholic dioxane solution at 60-700 leads
to a mixture of amino alcohols (XI) and (XII). There are 2 Soviet
references.
ASSOCIATION: Moskovskiy institut tonkoy khimicheskoy tekhnologii Im.
M. V. Lomonosova (Moscow institute of Fine Chemical Technology
imeni M. V. Lomonosov)
SUBMITTED; July 10, 1958
Card 2/2

Nazarov , I . N. , Prost aKc,; , N. S "iwh y~va N. N Fri -'k i.-.a :I-A
1 T L E S~-.%thesis of Halogentesub.9tituted 1,2,5-Trimeth~'!-,
methyl-, and Pi,~eridines
PERIOLICAL: Zhurnal obshchey khimi.', Vol 29, 'Ir e, PP TE c I,,
ABST:UCT: T'-,PrL are but little data available in publicati-:.s W~th
the -halo6en-su'lstituted piperidines. Or. the oaci-q A'
*
t
i.-~Cth
d of the
aecozidary and tertiary -i"Crldoles
alreauy devised by the aathcrs (Ref 2), they investi~at,d tr.e
sur,stitution of haioger. for the oxy-group of t1.,i,!sc- ~ip-ridine
alcohols. The pipEridoles (III) and (IV) used as iritial products
were converted by redirtiDr afthel.,Iperidones 'I) -,r-.d The
co:;:pouz,.ds (Va) and (VI) w,i-e ;ormed or, reaction zf the correspond-
ing piperidoles with thionyl chloride (7o',lj yield). In 'his wa~,
the mixture of the stereoisomeric
pi-ridlyien (Va) in furi,%(A from tho mixtare of thu, ;t- ic
1,2,5-trimettiyl-,'.-piperidoles (III) which is obtaine~-J by reduc-
tion of piperidone (I) with sodium in alcohol . In tnis f:rzt -
Lientioned mixture, one of the isomers is predominrint 7g,
. ~ ) , which
melts in the form of the picrate at 196-2ooozhe same isomer of
Card 112 the chloride (Va) was a Iso obta ined f rom 1 , 2, 5 -t ric--t h~ 1 - -T I -

S,ynthesis of Ra loge r-i-aho t itated 1,2,5-TrimtAtjl-,
, and 1-Acyl-2,5-di,-,.ethjl Piperidines
2,5-Dimethylt
peridole 0-aelting-point "12-730), which was separated from tne
mixture of the stereoisomeric piperidoles (111) (also in a yield
of 70;U')- In the same way, compound (VI) was forrrc~d which was
converted into (XVI) with acetic anhydride. Compound (Vb) r-sulted
on reaction of the pipcridole (III) with phosphorus tribromide.
The halogen-substituted derivatives (Va) and (Vb) can only be
distilled in the vacuum. On standing, and at 1300, they are
transformed into hygroscopic products. Further cheL.i.-al transfor-
mations of 1,2,5-trimethyl-4 and 2,5-dimethyl-4-chloro-piperi-
dine were carried out. There are 4 references, 5 of which are
Soviet.
ASSOCIATION: h1oskovskiy institut tonkoy khimicheskoy tekhnologii (Yc3cow
Institute of Fine Cnemical Technolo.-Y)
SJUITTEDs July 10, 1958
Card 212

5M SOV179-29-9-12176
AUTHORS: flazarov, 1. N.,Prostakov, N. S., Haskina, E. M.,
Mikheyeva, No N Stolyarova, L. 0.
TITLE: Synthetic knti-spasmolitio Substances. Synthesis of I-Phenyl-
I-eyolohexyl-3-(21,51-dimethyl piperidyl-41)-propanol-I
PERIODICAL: Zhurnal obahchey khimiie 1959, Vol 29, Nr 90 pp 2861-2864
(USSR)
ABSTRACT: 2,5-dimethyl-4-piparidone (II) (Refs 1, 2) obtained from an-
aonia, and propenyl-isopropenyl ketone (I) according to I. N.
N$zaroy, was made use of for the synthesis of compounds struc-
turally related to the efficient anti-spasmolitic Arthan.
(I) is an intersediate in the synthesis of anesthetics Promelol,
Isopromedol and a-Promedol (Ref 3)- Compound (II) was trans-
formed to (VII) according to Kizhner by reducing hydrazone
(III) Of piperidone (II) as well as by cleaving the piperidine
compound (VX) with wateri the latter compound to formed by
compound (V) and lithium. Chloroderivative (V) was obtained
from the reaction of piperidol (IV) with thionyl chloride.
Condensation of piperidine (VII) with acetophenone and form-
aldeh d according to Mannich caused the separation of ketone
Card 112 (VIII~ :hioh was further transformed into compound (IX) by
-QL-

SOV/79-29-9-12/76
Synthetic Antl-spasmolitio Substances. Synthesis of 1-Phenyl-i-cyclohexyl-
3-(21#5'-dimothYl piparidyl-it)-proyanol-i
the reaction with magnesium chloro cyolohexyl. According to
Preltnim ry pharmacological data by M. D. Hashkovskiy (VNIKhFI),the
chlorohydrate of this tertiary amino alcohol exhibits a
marked anti-spasmolitic activity and is but little inferior
to Arthan (Reaction' Scheme). To investigate the structure do-
penienas of this activity of tertiary amino alcohols con-
tainina the 2,5-dimethyl-i-piparidyl group as amine radical,
the authors synthesized propanols W, (XI), (XII), (XIII).
The synthesis of these amino alcohols was made with the al-
read) earlier described ethyl eaters (Ref 4) of P-(20-dimethyl
piperidyl-l)-proplonio and a-(20-dimethyl piperidyl-l)-pro-
pionic acid as well as with I-acetonyl-2,5-dimethyl piperidine
and the corresponding organomagnesium compounds. There are
4 Soviet references.
ASSOCIATION: Moskovskly inetitut tonkoy khimicheskoy tekhnologii
(Moscow Institute of Fine Chemical Technology)
SUBMITTED: July 10, 1958
Card 2/2

50)
AUTHORS: Nazarov, 1. ff., Prostakov, ff. S., SOV/79-29-9-27/76
Mikheyeva, ff. N., Mikhaylova, 9. M.
- -------------------------- - -A
TITLE: Synthetic Anaesthetics. Derivatives of I-Oxyalkyl-2,5-
-dimethyl Piperidine
PERIODICAL: Zhurnal obahchey khimii, 1959, Vol 29, Nr 9, pp 2940-2942
(USSR)
ABSTRACT: The 1-oxyalkyl-2,5-dimethyl piperidinea described in one
of the previous reports (Zhurnal obahchey khimii, 29, 2861,
1959) were used for the synthesis of their esters which
may be useful as anaesthetics of the methycaine and surpho-
caine type (meticaine? surfocaine?) as well as for the
synthesis of 1-alkyl halide-2,5-dimethyl piperidine, as
intermediates in the synthesis of the anaesthetics of the
phenadone group. Benzoylation of I-p-oxyethyl-2,5-dimethyl
piperidine (1), 1-a-methyl-p-oxyethyl-2,5-dimethyl piperidine
(II), 1-p-oxypropyl-2,5-dimethyl piperidine (III) produced
benzoatee of these amino alcohols, (IV), (V), (VI) (Scheme).
The oxy-group in the amino alc6hols (I), (II), (III) was
replaced by chlorine by means of thionyl chloride. The
Card 1/2 following piperidines were obtained in yields of up to 80%:

3ynthetic Anavlothetics, Derivatives of SOV/79-29-9-27/76
-I-Oxyalkyl-2,5-dimethyl Piperidine
1-p-athyl-chloride-2,5-dimethyl piperidine (VII)9
1-a-methyl-p-ethyl-chloride-2,5-dimethyI piperidine (VIII),
1-0-propyl-ohloride-2#5-dimethyl piperidine (IX). In heating
the latter with 30 alooholic alkali solution 1-0-ethoxy-
propyl-2,5-dimethyl piperidine (X) was aeparated inetead of
the expected product of dehydrochlorination.
ASSOCIATION: Hookovskiy inetitut tonkoy khimicheskoy tekhnologii
(Moscow Institute of Fine Chemical Technology)
SUBMITTED: July 10, 1'958
Card 2/2

PROSTAICOT, N.S.; NIIHMTA. 11.1r.
ftbotltuted pyridines. 2,5-dinothyl-4-phanylpyridine and Its
transformations. Ked.prom. 14 no.21ll-13 .1 160. (MIRA 13:5)
1. Noskovekly institut tonkay khtmicheelcoy takhnologit iment
N.V. Loconosova.
(PYRIDIII)

Rk?"v. 1.M. [deceased]; FROMM, U.S.; KIIHMTA, N.V.
PrePmratiOn Of ft mixture Of a promsdol base and 1,2.5-trimthyl-
4-phoul-4-plperldol. Mod.prom. 14 no.6.-26-30 Je 160.
(MIRA 13:6)
1. Koakovokly Institut tonkoy kbimichesicoy tak:hnologil loqui
H.Vl Lomonosova.
(PrMIDINA) (PIPEMINOL)

PROSTAIDDT. 9. S. ; M IVA, N.M.: IGUMTA. A.7.; ZIKIVA, G.I.
Substituted pyridiaes. 2,5-Dinettvl-4411,(-O)-tolyllpyridines
ead their conversions. Zhur.ob.kbin. 30 no-7:2294-2297
J'l 160. (MIR& 13:7)
1. Waskovskly Institut toakoy khimicheakoy tekhnologii.
(Pyridine)

PROSTAKOV, U.S. I -IfDaMM
As__Y.H.
Synthetic anesthetics, Separation of stersoisomeric 192,5-trimethyl-
4-phepa-4,:-piperidinols. Zhur. ob. Wilm. 31 no.1810EI-U3 JTA 161.
(PUPA
1)
143
1. Moskovskiy inatitAt tonkoy khImIcheskoy takhnologii.
(Piperidinol)

PROSTAKOV, N_,S.; MUMMA, N.H.
Space configuration of piperidine derivatives. Usp.khim. 31
no.10:U90-1226 0 162. (MIRA 15:11)
1. Mookovskiy inatitut tonkoy k-himicheakoy tekhnologii imni
Lomonosova.
(Piperidine) (Stereochemiotry)

PROSTAKOYt-1145-4 IWOMINATA, T.V.; MIKH=A, N.N.
Infrared so"tra of isomeric 1,2,5-trimethyl-4-phanyl,4-peparldinole
and the atructur) of the R -isomer of 1,2,5-trimethyl-4-phanyl-4-pe erid-
inol. Zhur.ob.khim. 34 no.lt234-237 Ja 164. (MIRA 17M
1. Universitet. cL-uzhby narodov imeni P.Lumumby i Moskovskiy gosudarst-
venn.vy universitit imeni M.V.Lomonosova.

PROSTAKOV, N.S.1 ZArISEV, B.Ye.; HIKHATIDVA, N.M.; MIKHEYEVA, N.N.
Spacial structure of isawric 2,5-dimthyl- add 1, 2, 5- trims thyl-4-
phanyl-4-piperidole. Zhur.ob.khim. 34 no.2:463-467 F 164.
OGRA 17 13)
_W,
1. Universitat druzbby narodov Imeni Patrisa Lumumby.

L~,(Or453-67
A I
F i~~021344 SOURCE CODE: UR/0372/66/000/002/VO54/VO54
AUTIIOR: Greysukh, V. L.; Mikheyeva, N. N.; Nadtochly, A.I. 39
TITLE-. Experience in realizing an inversion-type information retrieval system with the aid
of an electronic digital computer 16c
SOURCE: Ref zh. Kibern, Abs. 2V349
REF SOURCE: Nauchno-tekhn. inform. Sb. Vaes. In-t nauchn. I tekhn. Inform., no. 3,
1965, 21-26
TOPIC TAGS: electronic digital computer, information storage and retrieval/Ural-2
electronic digital computer
ABSTRACT: The algorithmization of an inversion-type information retrieval system (IRS)
with the object of utilizing it in electronic computem Is described and the advantages of the
coo rdinate-comparison retrieval method over the sequential retrieval method are pointed out.
particularly with respect to bulky documents for the purpose of assuring the flow of documents
to users without great effort on their part as well as of eliminating manual labor and accele-
rating the retrieval process. In addition, the authors form the class -of standard processes
Card 1/2 UDC% 518. 5:661. H2

L 05293-67
4td-Rit, AR6021344
into which the algorithm of the inversion-type IRS breaks down; this class may be utilized
in the solution of other information- logic problems. The developed algorithm flowchart of the
ERS corresponds to the special features of electronic digital computers and way serve as a
basis for developing a practical and convenient information retrieval system. The findings of
the experiments with the realization of an inversion-type ERB by tn"ns of Ural-2 electronic
digital computers also are presented. V. Kozlovtsev. I Translation of abstmetl
SUB CODE: 05, 09/ - __ -
COM 2/2

L 37226-66 E4T(1) J'.V/RO
ACC NR: AP6015395
SOURCE CODE: UR/0409/65/000/004/0531/0536
AUTHM: Prostakov, N. S.; ItUcheyeva, N. N' ; Fkhal'gumani, D.; '-,at'y-up K. D.
ORG: Peoples' Friendship University im. Patrice Ikmamba, Moscow (Universitat druzhby
narodovT
TITI,E: Substituted pyridines. Amidos and hydrazides of nyridinecarboxylic acids
SOnCE: lGiimiya goterotaiklichoskikh soyedinoniy, no. 4, 1965, 531-536
TOPIC TAGS: organic amide, hydrazine derivative, pyridine, aromatic carboxylic acid
ABS'LR.ICT: Pyridinocarboxylic acids obtained from oxidation of dimethyl-substituted
pyridine bases were used for synthesizing their amides and hydrazides, which are sub-
stances of pharmacological~,interest. The reactions are illustrated In the diagram:
1100C cloc (Cl 11S)INOC
I - I I
N C0011 '~~N COO
UDCt 547.826 + 542.95
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ACC Wo AB0020788 SOURCE CODE: 606-01~067006766:
AUTHOR: Greysukh. V. L.; Mikheyeva, N. N.; Nadtochly, A. 1.
TITLE: An attempt of realization on digital computers of Information search systems of
Inverted type
SOURCE: Ref zh. Matem, Abs. 2V349
REF SOURCE: Nauchno-tekhn. inform. Sb. Vses. in-t nauchn. I tekhn. inform. , no. 3, 1965,
21-26
TOPIC TAGS: computer theory, computer technirpie, digital computer, algorithm, in
storage and retrieval
ABSTRACT: The algorithm for an inverted Info rm ati on-sca rch system (ISS) applicable to
electronic digital computers has been described. It has the advantages of the coordinate-
comparison method as compared with the consecutive search method. This Is particularly
Important in the case of large masses of documents requiring tho arrival of documents to the
users without troubles arising from the side of the documents, and also with the elimination of
manual work and the general acceleration of the search process. In addition, two classes of
standard processes have been formed into which the algorithm for the inverted ISS can be
Card 1 2 .--- UDC; 5118~, 5,Q-81,J42---

W, AR6020788
decomposed and which can be utilized during the solution of other information-logical problejx
An algorithmic scheme for the ISS Is developed in such a way as to correspond to the peculi-
arities of electronic digital computers and can thus serve as a basis for the realization of a
practAcally convenient system of information retrieval. Results of experiments for the reali-
zation of ISS of the inverted type on electronic digital computers "Ural-211 are also presented.
[Translation of abstract ] V. Kozlovtaev

CHUMOT. T*T.; nachallmik.
Tomograph for the pre-war nodel of the X-ray upparatus mewifactured by the
OBurevestulkO plant. Test.reat.l. rad. no-3:78-80 Yq-J~ '53. Off-9A 6:8 )
1. Madmanchast' Chelyabinskogo metallurgichookogo saved&.
(L-raye-Apparatus aad supplies)

MIKUMA, V.S.
I
Study-tag tho mochantem of drying moist materi&la. Trudy KTIPP no.6:64-
77 156. (KM 10:3)
(Koleturs) (Drying)

,vi / ',~- // 'r- y, T t il, /V.,
USSR /themical Technology. Chemical Products 1-32
and Their Application
Food Industry
Abs Jour: Referat Zhur - Khimiya, No 9, 1957, 32937
Author : Mikheyeva N.3
Inst : Moscow Technological Institute of the Food
Industry
Title : Method for the Computation of the Duration of
Drying of Lump Materials df the Food Industry
Orig Pub: Tr. Moak. tekhnol. in-ta pishch. prom-sti,
1956, No 6, 116-127
Abstract: A correlation has been ascertained between the
critical and the Initial moisture content of a
body: Wcr - We =0.56 Wi, wherein Wcr Is the
C ard 1A

USSR /Chemical Teclinology. 1.c,?ruical Products
and Their Application
Food Industry
Abs Jour: Referat Zhur - Khimiya, No 9, 1957, 32937
reduced critical moisture content, We -- condi-
tional equilibrium moisture content and W1 --
the initial moisture content. This correlation
is confirmed by experimental data of the author
and other researches. By means of the derived
correlation between relative coefficient of.
dryin~.,(3(_ Wand the initial moisture content
X-= . ) j, a procedure has been worked out
for calculating the duration of drying under
any conditions of operation of convection driers.
C ard 2A

GINZBURG, Abram Solomonovichp prof.;, MIFJIEYEVA, Natallya Samenoyna;
BAB IYEV, Nikolay Nikolayevichi
GRACREV, Yuriy Pavlovich; ZITURAVIXV, Vyachealav Fedorovich;
DASHEVSKIT, V.I.; FEDOROV, N.Ye., prof., retsenzent;
MEGE4, P.V., dots., retsenzent; GORBATOV, A.V., dots.,
retsenzent; ROGOV, I.A., dots., retsenzent; KOVALEVSKAYA,
A.I., red.
[Processes and apparatus of the food industry; practical
laboratory workj Protsessy i rLprraty pishchevykh proiz-
B
vodstv; laboratornyi prELktikum, Byl A.S.Ginzburg i dr.
Moskva, Pishchevaia promyshlennost', 1964. 270 p.
(MIRA 17:12)
1. Moskovskiy tekhnologichoskiy institut myasnoy i molochnoy
promyshlennoBti, kafedra protsessov i apparatov (for Fedorov,
Rogov, Gorbatov). 2. Voesoyuznyy zaochnyy tekhnologicheskiy
institut pishchevoy promyshlennosti (for Seregin).

KUMETSOV, Vladlen Ivar;i)vl;-Y,; ' ; I "" .71 ~1. , red .
I. ---,
[Behlnd the Bj',,Jj.'rier,fA, -,I,- ;It,~ ! a r: ~ - C'I-
tami. moakva, IYO , I," , . I ~k, V, . I P11, . ~ ~~: I I "
~ I I

, NIKRNYETA, Oel,.- ZRABROKOVA, Z.A.; POPOTA. L.A.; UKINSKIT, I.N. [deceased];
i k -I- -
ICIRD, N.G.; TSVUVA, I.A.; SNDLIVATA, L.K,; IADYKOVA, M.P.;
USHITSM, A.D.
Blosynthests of tetracycline on enriched media. Ned.prom. 14
no.1:31-34 Ja 060. (KM 13:5)
1. Hoelrovskly savod meditstnekikh preparatov lo.1 I Toosoyuznyy
nauchno-lasladovatellskiy lustitut antibiottkov.
(TIMCYCLtU)

dualw; p A.L. j zaaluzhonn)rj vrach iSt"SR, kand.mod.nauk, rentgenolo,l;
H14&M-NA, 0 - n. p rentgenolog
Tenth anniversary of the death of M.D. A.D.Jtybinskii. Vest. rent. i
rad. 36 no.604 N-D 161. (RI-A 15:2)
1. Sanatoriya "Kavkaz", predsedatell Yeasontukskoy soktsii rentgonogov
(for Shafran). 2. Sanatorlya "Stavropollyo", chler, Yesgentuk-okoy
sektsii rentgenologov (for Mikhayova).
(aBIMAII, AILKS61 DIaTAlrV-i,;H, died 1951)

KANTORP Stara Mllihaylovna; B=YEVA,___Qqlga _Kasil_'yevn4;
zHEBRovsKAYA, A. , red.; VAYSKO, H. , red. izd-va;
GARINA, T. , tekhn. red.
(German-Russian dictionqry of most commonly used words in
technical literature] Nemetako-rusakii slovarl-minimum ob-
shchoupotrebitellnykh slov v tekhnichaskol literature. Mo-
skva, 1963. 29 p. OGRA 16:6)
(German language-Dictionaries-Russian)
(Technology-Teminology)
"WW

LOZOVOY. A.V.,- KRICHIO, A.A.: MIVSTV.A.,-H.P. --
Hydrogenation of enriched Baltic Sea region ShAlsh -juder low
presnurs. Xhim.i tekt.topl.i m9W nv.5:12-46 Iv '57. (MIRA 10:7)'
1. nAitut goryuchikh iskopoqezykh AN SSSR.
(BAltio 6ea region-ShFkIes) HYdrogenntion)

--- - SWAs RqL ---
Control meamwes for aiscocbqU leaf blIght of peas. Trwly VIZR
no.,24tl29-234 160e (MM 24:2)
(Latwia-Peas-Diseases aad posts)
Magi q pwupathogouic)

~ - "2A -I -
I
MMIEYEVA' R.I., starshiy nauchayy sotrudnik
Leaf mold of beanp. Zashch..-ast.ot 7red.i bol. 7 no.5:;7-28
Yq 162, (MBA 15: 11)
(Latvia-Beana-Diseases and pests) (Latvia-Botrytio)

I
- MUMMA, Seraftma fadorovaa; SWOROT. 1.W.. red.; ZMOVA. TOO,
takhn.red.
[Konapolies In the British iron and steel industries) Konopolii
v ane,111skot chernol, metallurgil. Leningrad. Leningr.univ.0
1960. 77 P. (KIRA 14:1)
(Great Britain--Steel industry)

1~10j
SUBWTA, V.S.; MIXOMA. S.Z.
Studies of toxigenic stgvhylococcRl culture on solid media; Puthor's
abatnet. Zhur.mlkroblol.opid. t immun. 29 no.2:116 7 15A.
(HIRA 11:4)
1. Is Gosuderstvannogo kontrol'nogo inatitutn eyvoratok f voktain iment
Tarnsevicha.
(MICHOCOCCUS PYOGEM, culture.
on solid media, toxin-prod. strains (Rua)

/t,f, /
y, rL , -4 /-,- -
SMOBIL'TSTN', Yu.T.; KIKHMTA, T.G.; KOGHETKOV, P.P.; KODOCHIGM, D.I.
11~~ -
41M
Rural hydr r pever stations on the small rivers of the Hari
Republic. Isv.Mar.sta.po slek.sel'.1 les.khos. no.l: '51.
(KIRA 10-11)
(Hart A.S.S.R.-Hydroelectric power plants)

// E YE Vlt -7 - 14-
Ifliff"A, T'.G.'
,----0,T
Technical and economic Indices to operating the Vartasekays
locomobile rural electric power station. 1%v.Msr.staiPo elek.
9e1'.1 les.khos. no.1:39-49 151. MIRA 10:11)
(Mari A.S.S.R.-Slactric power plants)

-ey -;"
SKOBILI
s'.
4,1-:;, lc~;,
-~ NINUMA. T.G.;
Yu.V. ,
NOCHETROT. P.P.. KODOCHIGOV, D. I.
Local rural electric power systems based on the example of Norl-
Tursk Region of the Karl A.S.S.R. Izv.Nar.sta.po elsk.sell.i
les.khos. no.1:51-81 151. (NIRA 10:11)
(Karl A.S.S.R.-Blectric power plants)

/I A~- /,- ~11~' 11, 6,t.
MIXHNMA. T.G.; SHIRROV, R.V.
Operational Indices for rural electric Dower plants. ltv.nar.
ste.po alsk.991.1 loo.khos.no.2:5-21 053. (MIRA 10:12)
(Blectric power station)

/-/ // "'o.-, " ~ "I- - ~,;- , ~' - i , ) (1,
SXOBZLITSYV, Tu.T.; HIMMYBVA, T.G.
Power consumption of the agricultural districts in the area of
the KWbyahev Hydroelectric Power Station. Isv.mar.sta.po slek.
zel.t les.khos.no.2:51-66 '53. (min 10:12)
(Electricity in agriculture)
(Lqbyshev hydroelectric power station)

MIKHffXVA. T.G.
--'0 ~=Justlng the load graDhe of rural consumors and matchirc then with
oooo~ the-gftphs of Industrra-rpower,okst'49s. Isv. Kazan. fil. AN SSSR.
-Ser. anerg. I vo4. . khosI. no.1:43-70- 1579 (MIRA 11:10)
(Alectric power distribution)

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