SCIENTIFIC ABSTRACT YURYEV, YU. K. - YURYEVA, M. S.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001963220017-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 19, 2001
• Sequence Number: 17
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

ZEFIPOV, N.S.~, IVANOVA., R.A KECHER, R.11 YUOYEV9 Yu.K*
---~-Xenea. fart 18: Wa-Enp
3,O'-.ndoxcc3TIc.l,m.xa--es and -a-yccl~ .-r zperl';elm
L- - " _~,Jyl - nd -,,' dl -- 1-
rearrangement during ?,ajoEena-4Cn Cf it r>- t?~7-
3,6-endoxocyclohexenedicarbQxyl.!c at-id:I. 71il-Ir. ob. khlm. 35 no.l.,.
61-67 Ja 165. (MIRA 18-2)
1. Moskovskiy gosudarstvBnnyy universite'..

ZEFIROVY Nos.; DATIDOVA, A.F.; YIT0YEV,,'
3.6-Endoxocyclohexanem and -cyc1chexenes. Part 21~ Stereochemistry
of bromination of 3,6--endoxod1hydrophthalic aoid and its dimethyl
ester. Zhur. ob. khIm. '~5 no.5i8l"22 My 165. (MIRA 18t6)
1. Moskovskiy go sud ar sitvennyy universitet imeni Lomonosova.

ZEFIROVP N.S,; PRIKAZCHIKOVA,. L . P. X q~R
3,6-Endoxocyclohexanes ani -cy-alchexenes. Part 22: Stereochemilstry
of oxymercuration of diniotwhyl aster o' 1-methoxY-3,6--endmotletra-
hydrophthalic acid. Zhur. ob. khim, 35 no.5,822-827 9
-Y 165.
(MIRA 18:6)
1. Moskovskiy gosudarstvennyy univerBitet lzeni Lomonosova.

DATTILOVt S.N.p gla,r. red.-., ARBUZOVj A.Ye., rod.; VVEDRISKIY, A.A.p
red.; VENUS-DANIWVA, E.D.p red..-, ZAMAJ10VA.A.I.., riod.;.
E
IOFFLI, I.S., red.; KAVMZflEVA, Ye.D.,, red.; LUTSEFF0, I.?.,
red.; MISHCMIKO, K.P., red.; NaITSOV, M.S., red,,; FUROV,
A.A., red.; FREYDLIIIA, R.Kh.., red.; SIRIYAKIN, M.M., red.;
SIIUKAREV, S.A., red.; YURIYEV, Yu.K., rod.
[BiologicaLly active compounds] Biologicheski aktiMye
soedineniia. Moskvap Naukay 1965. 305 p. (MIRA 18:7)

Y-tu~,-IUA-4-BAZANOVA, IV. N.
ZEFIROVP KADZYAUSKAS, P.P.;
Estr derivatives of
Cblorination sternocbemi y of 5-r-Ilar mercuric lie
dimethyl ester of 7-oxabicyclo[212pl]-2t3-heptrnedicar!)OXY,
acid. Zhur. ob.,khim. 35 no.8:1499-1500 Ag 165. (KRA 1W)
I. 1.4oskovskly goqudarstvennyy universitet.

ZEFIROV, N.S.; KRUTETSD-YA, CU.; PRIKAVCHMOVA, L.P.4 YURtWf, Yu.K.
I v
m

L 1817-66
AXCESSION NR: AP 502 S T 2 7 'IR/1)(I 7q /0 1, M 35 "0 IV 1901 7/1811
j ;
~47.592.14.2~~47.463
7~, r- V P
F I I .TI!Ire K A
I rLE 3, lj-Fndooxacyclohexane~; and 28~ Renct Inns nf Pxn- and
i 2 2 1 cy r- I ollej) t ane - 13- d i c- a ribo xv 1r
SOURCE: Zh u rn a I nbsh chey kh iml i , v. 3 5 , no. 10 196 5 , 180 7 -1811
TOP I C TAGS: oxabicvclIc commmind, heterocyclic compomd T Art inn w.-hFmjqM
FA C-T Tjj rk j ; 1
take place because the back-side auvroach of ttle ilucleophile pre(eedin2 the Walden
- -I ~. - ut.~r navid. ~quxr~ Lu~ iurmai.-Lun
(if a Dianar caT+OnILIrD-frn fntp,~Afafo, prpvantar! by the rigid F-ge 9 t r~ sr r j re .

47
-,f- T

?i p AJ 5 0 2 5 1
-T F
Y, 17 6C

TSUKERMAN, S.V.; KUTULYA, L.A.; SUROV, Yu.N.; LAVRUSHIN, V.F.; YURIYEV
Y
Basicity of furan, thiophene, and selenophene analogs of chalcone.
.DakI. AN SSSR 164 no.2:354-356, S 165. (KIn 18:9)
1. KharIkovskiy gosudarstvennyy universitet im. A.M. Gorlkogo i
Moskovskiy gosudarstyennyy universitet. Submitted Parch 1. 1965.

GALIBERS11TAMO HsAs; KFAGHATUROVAs G.T,; NOVITSKIY, K.Yu,;
YURI"b YUOK.
Reactivity of 5-nitro-2-aMor=ethy1furan and
5-nitro-2-chlcwomethyloolenopliom. Vest* Moske un, Sero 2t
Dim, 20 no,083-85 Jl~Ag 165. (MIRA 18:10)
1. Ke.fedra organicheskoy khimli Mookovskogo gosudarstvennogo
universiteta.

T5UKERMN, S.V.; ORLOV, V.D.-, LAVIRIUSHIN, V.F.,,.YU i12VA Y ~U- K -
Synthesis of nelenophene analogs of chalconem. Zhur. org.
khim. 1 no.4:650-653 AP,165. (MIRA 1.8tll)
1. Kharlkcriskiy gosudarstvennyy universitet imeni GorIkogo
i Moskovskiy gosudarstvennyy universitet imed Lomonosova.

L 38217-66 EWT(m)/E4P('J)/r DJ/RM
ACC NR: AP6025463 SOURCE CODE: UR/0080166/0391007/1638/1641
AUTHOR: Kobzova, R. I.; Oparina, Ye. M.; Levkina, N. K.; 111~gd~slyeva. U. N-,,
Yur'yev, Yu. K.-
ORG: Moscow State University im. M. V. Lomonosoy (Lpsk6vskiy gosudarstvennyy
universitet); VNII NP
TITLE: $-Diketones nd azomethines of the selenophene%eries: oxidation Inhibitors
for silicone fluids
SOURCE: -Zhurnal prikladnoy khimii, v. 39, no. 7, 1638-1641
TOPIC TAGS: antioxidant additive, silicone lubricant. selenophene, selenium compound
ABSTRACT: A study has shown 0-diketone and azomethine. derivatives of gelenophene to
be effective thermal-oxidation inhibitors for silicone fluids used as lubricating
oils1land as dispersion media for lubricating greases. Selenophene derivatives were of
interest because compounds containing a selenium atom in a ring are more thermally
stable than the conventional antioxidant dilauryl selenide. Nine compounds were
teated for't;ntioxidant effectiveness (criterion, gelation time) in various silicone
fluids at 300C. ' For polymethyl(chlorophenyl) sil"ane OMP9)1 the moat ef fectiva
acetone, and for polymethylsiloxane
antioxidant was (Z
polymethylphenylailoxane (FM-1322/300),the most effective were N-salicylidene-
Card 1/2 UDC; 546.3-19:66.022.37

L '38217-66
ACC NR. AP6025463
(2-selenophene-yl)amine and dipicolinoylbis(Z-acetylselenophene)- With Increasing
concentration of the antioxidants (0.5 to 5A their effectiveness increased. Orig.
art. has: 1 table. [SH]
SUB CODE: 1l/ SUBH DATE: 2ljan65/ ORIG REF: 007/ OTH REF: 0011 ATD PRESS:
0 Ley

KHARITONOV, G. N. YE
dur
no.
1. TSentrallnyy nauchno-issladovateliskiy institut mekhanizatsii
obrabotki drevesiny.
(Loading and unloading) (Wood-Preservation)

NOVITSKlY, K.Yu.; KRACHATUROVA, G.T,- GALIBERSHTIJI9 M.A.; KANDRORp I.I.-
YUR
Sypthesis of some chloromethyl compounds of the furan series.
1. Kafedra organicheakoy khimil Mookovskogo univereltet-ao

ZhTIROVP N.S.; DATIDOVA, A.F.; YURIYEV, Yu.K.
Stereachemistr-
3,6-Endoxceyolohexanes and -cyclohexenes. Part 23 y
of chlorination of dimetlwl esters of 3.6-endoxotetrahydrophthalic
and -dihydrophthalict~M in n'onpolar-solvents.
Zhur, ob. khim. 35 io5a -.- - , --- , RA- 18 -, 8,1
I. Moskovskly genudaratvennyy univernUct.

KUPRIY&NOV, P.A., prof.;-KRUNKO, I.L.,, prof.; BALYUZEK, F.V., GLEW1,
Yu.j., SKORIK, V.I.- FAPSHATOV, M.N.- YUR~~,_Y%N.
Use of the artificial circulation method in traumatology. Vast.
khir. 89 no.8:3-8 Ag 062. (MIRA -153-10)
l Iz 1-y khi gichaskoy kliniki usov'ershenstovaniya vrachey
(;ach, - profr.urP.A,Kupr1yanov) i kliniki travmatologii i ortopedii
(nach. - prof. I.L.Krupko) Voyenno-meditsinakoy ordena Lenina
akademii hi. S.M.Kirova. 2,Deystviteltnyy chlen AM SSSR (for
P.A.Kupriyanov). 'Adres avtorov.: Leningrad,, pr. Karla Marksa.. d.
5/20, 1-ya khirugicheskayakllI4ika usovershenstovanlya vrachey.
(BLOOD-CIRCWATION ARTIFICIAL)
(TRAUMATISM)

OVCHINITTIKOV, Yu,I,; YUHI TEV, Yu.N.
Intrameous anesthesia using neuroplegics, Vest, kbir, 90
no, 5:105-110 My'63 (MIM 17:5)
1. 1z kafedr-j travr-atologil i ortnpedii (nachallnik - Prof. I.L*
KrupIko) Voye- -lo-medits-Inskogo orflona Lenina. akademii Imeni Kirova,
Adres avtorov., Tenbigrado K-9v Botkinskaya ixl,,, 13., klinika trav-
matologil i ortopedil.

YURIYEV, Yu.N.; SHANIN, YU.N., kand. med. nouk
Automatic endotracheal other anesthesia inorthopedic operations*
Ortop. tre;vm. i protez* 24 no.6t1843 J0263 (HIRA 16:12)
1. Iz kliniki ortopedii i travmatologii, (nachallnik - prof.
L.L.Krupko) i kafedry anesteziologii (nachaltnik - deystvitelf-
nyy chlen JU41 SWR prof. P.A.Hupriyanov [deceasedD Voyenno-medi-
tsinskoy ordena Lenina akodemjA imeni S.M. Kirova. Adres Yurlyeva:
Leningrad K-9. Botkinskaya u1.,, d-13, Klinika travmatologii i
ortopedii, Voyenno-meditsinakoy ordene, Lenina akademii imeni
S.M.Kirova.

NOVITSKIY,, K.Yu.; YURIYE;Vp Yu.K.1 ZHINGAREVA9 V.N.; IMR07Ap Ye,F.
Synthesis of sy=etrical 31.4-bis (dialkylamino-metlwl)-furans.
Dokl.Aff SSSR 148 no.4s856-859 F 163. (KM 16W
1. Maskovskiy gosudarstvennyy universitet im. M.Lomonosovas
Predstavleno akademikom A.N Nesmepnovym.
iFuran)

xTril .00 I.L., prof.
wmnts in orthopedies and tra=atolog7o OrtGP*,v
Use of =scle rel .8...43 161. (KERA 143-10)
travm.i protes. -no*10:3
1. Iz kafedry travmatologii i OrtOP6dii (nacTa'~ - Profe I*L*
Krupko) Voye=o-meditsinskoy ordena Laninaskadenii Ime S-K*
Kirovao
(MUSCLr.. RELAXANTS) (ORTHOPEMA)

KMJPKO, I.L. prof. (Leningrad, K-9, ul. Smirnova, d.8.kv.5);SHMIV, YU.N.,
dotsent; YURIYEVp Yu.N.; OYCHINNIKOVI Yu.1.
Some problems of anes'Unesla and,,resuscitation Ln traumatologyo
Ortop. tram. i protez. 24 no.6t72-81 Jel63 (MIRA 16:12)

PUPKO, V. Ya.; MALMO V. A.; GUSAKOV, I. M.; PETROVSKIY,-V. L.: DMITRIYEV; V. M.;
YURIYEV, Yu. S.
"Soix- problemr, in thQ devt~~-Ioppicnt of a thertaionie research converter."
report to be presented at Intl Corif on Thermionic ElectricU Power GQncration,
London, 20-24 Sep 65.
USSR State Comn for Applicationa of Atomic Energy) Moscow.

YURIYEV,Z.
young students of local lore in Ukhta. Geog.v. shkole 18 no.4.
JI-Ag 155.
(Ukhta, Komi A.B.S.Hr-Natural history)

L 24~17-66
AC~ NRI A?k067'57 SOURCE CODE: MV3158165100010.-IIOOOV0017
j'a;,4'jiOn: nTLoj V. Ya.; M kh A-; Gy )v, M!~o~vt_jy~ Dmit
V. M.; Yur'yevp Yu. Ss
0161: i4sics and F(:Wrr IiMftute, State Committee on the Use of Atomic Energy SSSR
energii SSSR)
TITLE: Certain.problems in the development of a thermionic emission reactor converter
SOURCE: Gbninsk Fiziko-energeticheskiy institut. Doklady,' no. 27, 1965. xekoto-
ryyc problemy ra;rabotki termoemissionnogo reaktora-preobrazovatelya, 1-17
TOPIC TAGS: thermoelectric convertor, neutron physics, nuclear reactor, volt ampere
characteristic
ABSTRACT: This is a review article dealing with several neutron-physics and engineer-
ing problems connected with the development of a thermithe converter in which heat
energy is converted into electricity-by using an electron emitter in contact with the
fissioning material of a nuclear reactor. Tha first section of the paper deals with
possible neutron-pbysics ebaiacteristics of such reactorsp such as the use of fast or
slow neutrons in the reactor, the dependence of the U-2-35 charge and the volume of
the active zone of thermionic reactors on the concentration of the uranium in the
active zones for different thicknesses of the beryllium reflector and for different
cathode materialop the distribution of the energy release over the active zone, the
Card 1/2

I I ROOM
L -,1431'7 66 -
ACC NRe AT(,006757
degree of burnup, the dimensions of the active zone, the critical reactor loads and
the type and amount of moderator. The second section deals with thermodynamic and
electrical engineering problems involved inguch a converter, such as losses, thermal-
efficiency, conversion efficiency, volt-ampere characteristics, and methods of minim-
izing.the losses. The third section presents the results of reactor tests of three-
element assemblies of thermionic corm!rterss made in the loop channel of the reactor
of the first atomic electric stations of the SSSR. Teats were made an different fuel
rods both under diffusion and are-discharge conditions* F~r the,partlaular reactor
tested, the losses annunted to 12% of the theoretical output power for ohmic electrode
resistance and commutation, 10% for heat leakage from the cathode, and.5% due to the
axial inhomogeneity of the heat.raleace in the assemW. We reduces the theoretical
power rating of 2-7-~-3 V/cmF to a value of 2 w/cuPs OrlS, ~rtv hiss a figures.
MM CODE:IJ20/ OBIQ FW: 002/ OM MWs 004

SfLGM 04yel ~'VJOTIA,

Card 2/2

candf4da" wicla Occ CUV
d4fts. A. Y!q.'fiYA tkild 1. Kllltlltliwv~
AU) Ml. No, 4, , N1 I.- Affor wr*i-il
4 to 04# 4J.'fa
it
to piewiti'M OW "414 .-t ii...
I~
of the "I. S. 'a
00
to a
(so
00 J;
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COS;
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rj-u t% AV 20 All a q a K C93 Ifft oil

/ 7-7 1- ~, r- -5,
7
Y~~ v
PLOTKIN, M., bizh.; YMIYU-KIKMM, B., inzh.
Fire safety separations of gas furnaces. Pozh.delo 3 no.12:7-9
D '57. (MIRA 10:12)
(Furvaces-Construction)

A-.*'P. .-YURtIVIA
MW ---- --
OUse of'. Rmarase for Determining Malic Acid,"
PyatnitoYdy, A. Pi XWyeval Ch(V'R Vibp
All-Union Inat of-Toba:oao and Idootirflim, Chair
o f Chcz, Krapnochir Padagoglcrll Imt, 4~" I)P
ltaokhim" Vol XIV, Ne 3 -
Detailed auantitative research for determining
malic acid, Iesed on conversion of the acid Into
fumarase which is obtained.in the foin of f=rath
Bitable materials
of mercurous oxide, was made on vo o
particularly on the leaves of tobaccol Obtained
tollowirZ data! Green tobacco contains from 5.5
to 13.8% malic acid; -tobacco, from traces
to 8 8%. Green makhorka contains 11.06%; cured
makho;i~, about 5%. SAmitted 15 May 48

ZAKHARKMI O.A.; KOLDAYEVA, T.N.; LISOGURSM, 2.1.; SKOVORODKY11, P.A.;
POLYAK, M.A.;-)9L9'YffA I uchastiye: GAVSHINOV, I.I.;
~ A.K.; PrInimal
SAVINA, A.B.; ALEWORMf Yu.A.; SP=OVA,, A.M.
Some peculiarities in preparing rubber mixtures in a two-speed
rubber mixer. Kauch. I, rez. 20 no.10:39-41 0 161. (MIRA 14:12)
1. Yaroslavskiy oh, Lnnyy zavod.
(Rubbe:r industry-Equipment and supplies)

7_
28951
A051/Al,
ALTHORSt Zakharkin, O.A. Xoldayova, T.N., LlcoSur4kly, Z,I., .2.1-10vorodkin,
P.A_., Folyak, M.A.,Yur'7ova, A.K..
Tr.7L-'7: Bona poouliaritioa of tho propzraticn of rubbor mi--cs, in a tilo-apCd
rubbor mixor
Fx- MODICALI Kauoh%L% i razina, n6. 10, 1961, 39 41
Irl X"A! I Expcr1rcnt4 wqro ce:i.duote4 on Uio rtw two_tpacd rubbor vIxerAP-Cv-140
mrnufacturcd at tho zt%vc4 ('1-U,7cv
B,~ldina_?Wt) "Bol'rhovik", ac~iordin~; to Uzi,~w; of t1ho Ita ro-
tora have 1c,~.-16/W.-j6 end 0.5 rpn; rnni"etivaIx. oftho mix-
in.7 ohmmbor la ~A5 litoro, tho.ol.ro of tho Lpcoa botwoon,tho blado* of-th,5 ro-
ta th N ar vi-ntz
tar. and +he wall. of tho mIxing ohambor 6-7 zn, Ron-vi of a a, p I
j7howed that whcn proparing oaviNsi_brca%-.-r ml=) In the nibbor vixor At, 40 rpa &A
a mixinS duration of 1,5 min without t-r-%int; into aoooimt the loa4ina and un-
loading, and a apeoifla proaaure of the uppar preD3 of 3.T'kc/c=2, the 4olumo 6f
tho load may ba brought to 165 1.1,tora without impalrinS the quality of tho mix.
The loading ooerflolent of the ohar~bor of tho UU.140 rubber mixer is 6%; Thun
Card 1/2

Somo peculiarities of the preparation ... A05 /A129
the 6ffact of the loadinS vol,=a wa3 ohoclcd and tho optim.= value (165 1) can-
1-cr mixes b-zod on 100,1 IM and conbination3.of It
flr..od for the canin5 and bo:0.
with CKS (MM), alao for troad rl=3 bamscd on 200;1 butadicno-Ptyreno ruVozara.
The 1.5 min duration time is ro(sommandcd for the onain,--and broemkor mixes In Ono
atago at 40 rpm of the rotor with an introduation of aulfur In the 64-inah rol-
a b&cod on 100% bu
lers..Condition* for proparint; 'tread mixon tadicno~tstyrana rub-
bars intwo cyol*3 are re0occ-ag -Adod. 'Mo potniibility of =ing the PC-a (M2)
rubber raixora avallable, attho ylpnt In poInted out in order to aooomplirb tho.
second oyolo'of mixing of tha troad mIxoa as wall oA Introftation of siLlfurcrid
accoleratorn. The follouing pcjr&on3 took part In-the work% T.J. Gavshinov, A.S.
'A, Alsksandr6v, AA, Somanova. There are 4 tablan and 10 Saviet-bloo
Savina, Yu.
refercnoo3.
ASSOCIATIONs Yaroslavskiy dh1svVy rAvod (Yaroolayll Tim Plsnt),
Cmd 12/2

FOLYAKS M.A.; EFSHTEYN2 V.G.; LISOGUIRSKIYv I.Z.1
~ZAMURKJN O.A.;,WWAYEVA, T.H.; Prinimali uchastlyes
SKOVORODKiNI, P.A,.; GAVSHIIJOV, I.J.; MINEYEV2 A.N.; SURIUNDUYAy
M.N.; BORISOV, -N.V.
studying the.prweas of rubber mixture preparation in 20 r.p.m.
rubber mixeri. Hauch.i rez. 22 no.46_10 Ap 163. (MIRA 16s6)
1. Yaroslavskiy i3hinnyy zavod i Yaroslavskiy tekhnologicheskiy
institut.
(Rubber) (Rubber machinery)

YUR'YEVA9 B. F., Doo Med Sci "Morphology of the hop-ling
processes in pulmongiry tuberculosis." Kiev, 1961. (Kiev Order
of Labor Red Banner-Med Inst im Acad At A. Bogomola~j M,
-8`61, 258)--
425 -

STMIV SILI; SUBOTSKAYA,v I.R.; ILYMM, S.D.; YURIYEVAP B.N.
Ozocerite therapy of infla =-tory diseases of the female sex-Lal
region. Vop. ku:r.t fizioter. i lech. fiz. kmllt. 24 no. 4:355-
357 J1-Ag 159. (MIRA 13:8)
1. Iz Taganskoy.polikliniki Upravleniya kbozraschotnymi
lechebnymi ucherzhdeniyami Mosgorozdravotdola (glavnyy vrach
L.M. Yakubson) i iz TZentralIncy khImiko-bakteriologicheskoy
laboratorii (Zav. D.I. Raskurazheva).
(OZOCERITE--THERAPY USE)
(GEIMVTIVE ORGAIS, FEMALE-DISEASES)

SVET-MOLDAVSKAYA, Ye.D.,- LEYKIIIA, S.D.;, YEVA B - 11
1!~~
Treatment of urogenital trichamoniasis in w=en try electrophoresis
with osarsol, Vop.-kur,., fizioter i leoh, fiz, kullt. 26 no.3:25/+-
255 MY-Je '61. (MIRA 14:7)
1. Iz Taganskoy poliUiniki,Upravleniya khozraabhetnykh lechebnykh
y vrach G.A.Valmik).
uchrezhdordy Mosgorazdrava glavny %z
(TRICHOMONIASIS (ELECTROPHORESIS)
(GEMOURINARY ORGANS-DISFMIS)
(ACRURSO17-THERAPEMIC USE)

KOZLOV.9 L.A... assistent (Ka,,mn'); SADYKGV, B.G., aspirant (Kazan);
GUSINA, A.A., vrach-kursant; SHISIffMA, G.G., vrach-kIlicaant;
X~~ - -karsant; KAPLUU., V.M.(Ma na Sakhalire)
.Pqe., Vrach
Discussion. Kaz.med.zhur. no.1:102 Ja-F.163. : (MIRA 16:8)
1. Akushersko-ginekclogicheskiy tsikl Novokumetskogo gosu-
darstvennogo instituta dlya u3overBhenstvovaniya vrachey
(for Guseva~ Shishkan, Yurlyeva).
(No SUBJECT HMIMS)

yag
G.Yu.
Role of reactive groups of proteir. complexes iu the stimulatiou of
[with Mmary In Inglighl. Blofizika 2 no.6.665-669
taste receptors
1579 (HIRA 10:10
1. Siologo-pochveunvy fa"lltet Mbskovskogo gowularetvaunogo uni-
versiteta im. N.V. Lomonosova.
(T0HGUR--INMVATIO9):__,(MMAPTO GROUPS)

YURIYEVAt G.Yu,
_Aole Of -the _iea-ctjvb-gr-oi- -f toin in--gustatory re ception. - - -
o, -pro
,Fiziol. zhur. SSSR 46 no~, 9tlM-1075 S 160. (MIRA 13;10)
1. From the Chair of Aninal and Human Physiologyp Lomonosov
State Universityt Moscova
'GUE
(PROTEINS !N THE BODY) (TON -INNERVATION)

YURIYEVA, G. Yu. Cand Biol, 501 - "on the problem of the enzyme-ohemical basis
it
of gustatory sensitivity0 Yoe, X961 (Inst of Normal and Pathological Physiology#
I M.A
Aoad-~ci USSR). (KL, 4-61, 193)
1 I\
-145-

G YU
.Recent data on the role of slulfhydryl groups of Proteins ih patatOI7
gensitivity, Biofizika 6 no, 2:172-176 161# (KM.A 14:4)
1. Biologo-pochvennyy fakulitat Mookovskogo,gosudarstvennogo
universiteta imeni 14.V, Lwbnosova6
(MMAPTO GROUP) (TASTE)

T. A.
tures. HIed. sestrav MOsk7av UO 9:18-24 1951*
(GLML 21.
Vertebral frac .1)
1. Candidate Medical Scienceils

bFR4 FY--' fF-.
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Intravpnous sodium pentotpal iLnesthesia in 6 *1121c and und'3r
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Yur'Yeve., L. A.
"The role of the nervous system In the pathogenesis of tetanus."
Kazan' State Medical Inst. Kazan', 1956. (Dissertation for the degree
of Doctor in Medical Science)

IV
USSWMmsn and Animal PhysioloMr. The Nervous System. V
Aba jour: iw. zhur-Biol., No 60 1958, a7441.
lu
-Author LOA; Yur.,
29r5; IMedical, Institute.
SIM
:7 7,Zjjjlj:
Orig Pub: Tr. Chkalovskogo med. in-ta., 1956., No 5, 302-310.
Abstract-. In preliminary experiments upon T dogap ccmditi=4
reflex glucosuria was obtained upon 7 to 10 combi-
nations of an indifferent stimulus (noioe and
light) with the injection of epinephrine (0.5 to
1 ml of a 1:1000 solution), and,, discrimination was
established. Immediately after partUa removal
of the pamtbyroid Wand . convulsive fielzures
were cbserved in all of the dop follming the
administration of adrenalin in embinaticin with a
Card 1/2

V
UswLiLmran and Animl IMs'ology. The Nervous system.
Abs Jour: ]Ref. Zium-Biol-) 11o 6, 1950A.- g7441.
In the presence of latent tetanus
Positive sigml~d between seizures the anijms" dis-
and ir tte peril distinctlY. Discrimination was
crillir,ated rti='U the degree of development, Of
disturbed according to last day Of life the emi-
aims of tetanus. On the to any mcci-
th convulsive aeizures of condi-
reacted wi. a eatablisbmMt
11 t
dental external amuts. cative of
tet4UWS is indl
tionea-reflem of tbis ase"O State.
reflex nature
Card 2/2

USSR/Human and Aniral Physiology. The Nervous System. V
Abs Jour: Ref. Z12ur-Biol., No 6, 1958, 27442.
tion between tones of 595 and 60) cyclesj a study
was mad.;. of the effect of the discrimination sti-
mulus prolonged.up to five minutes; its intensity
was incresadd.. and the discrimination stimulus of
increased intensity was tested for one month. The
extent and duration of the signs of neurosis (re-
duction in the magnitude of positive reflexes.,
disinhibition of discrimination refl"esj, disturb-
ance in strength relationships, ate.),, which arose
parallel with the diffimIty of solving a problem,
corresponded to changes in the fasting blood sugar
level (hyperglycemia) and the dynamics of the gly-
cemic curve (which had not returned to the initial
level after 150 minutes). NormlIzation of higber
nervous activity was acconpanied by the restoration
Card 2/3

USSR/Human and Animal Fhysiologd-. The Nervous System, T
Abs Jour: Rof Zhur-Biol., No 8, 1958, ~6907-
Author Y r' a,
Not i hicalovok Vcd~cal Institute.
Titlo, -. Vogetativo Rofloxas in Totanic Ohildron.
Orig Pub; Tr. Chkalovskogo mod. in-ta, 1956 vyp. 5, 311-315.
Abstract: Following tho onsot of totany in children tho
author observed a loworing of the vogotativo roac.
tions (oculocardiac and solar rofloxos, orthoclino-
static and hydrophilc tosts and othars) and their
paradoxical or ultrarlaradoxical character. A fow
days later this condition changod - tho roactivity
of tho vogetativo norvous system (WISS) incroasod,
with morc froqucnt prodoninanco of tho sympathetic
tonus. Thcro was an disturbance in tho synorgetic
Card 1/2

to T
ussR/Humn and Animl Physiology. Tho Norvous SYS m-
No 8, 1,958, 36907.
Abs Jour: Rof-Zhur-Biol.)
action of botli parta of' thc, VNS. j~pparontly thollo
c1langos appoar as a rosult of disturbancos in tho
rogulating action of tho CtM upon tho highor contors
of VIM (dioncophalic portion of tho brain).
Card
121

USSR/Human and linimal Physiolo&v Nervous System. T-10
Abs Jour Hof Zhur - Biolo, H:) 7., 1958s 32126
Author Yiirlyeva,, L.A.
Inst ----------
Title Condition of Some Unconditioned Reflexes During a Tetany
Attack.
Orig Pub Tr. Chkalcvskogo med. in-ta, 1956., 5, 316-318-
Abstract Attacks of tetany in children were accompanied by retarda-
tion of the CNS down to its lowest sections. This appears
in the disappearance after the attack of some undonditio-
nod reflexes both orientating (on sound, on stimlation of
the skin) and defensive (blink-ing, sneezing) and others).
Reflexes were restored in 5-10 minutes.
Card 1/1

GOLOVIN, YeAl YIJRIYEVA, L.A.
s a,!tt-,,,It- of
ore
zcne. mo. 15 sf* 87 1~

w'~ =7 = I
NOVOS=TA, A.T., otv.red.; TOLMOTICH. S.I., red.; GMUSIMOT, Ya.l.,
red.; YURIYAT, Tu.K.., red.;','MR-.'Y3TA. L.P., red.
(Department of Chemistry of Moscow State University] lhini-
chaskii fakmlltet Koskovakogo ordena Lenina i ordena Trudovogo
Irasnogo Zuamaui goeuderstvwanogo universiteta imeni K.V.Lomonoso-
Va. Koskva, 1955. 39 P. (KIRA 13-.6)
1. Koscow, Universitat,
(Kqecow University) (Koscow-Ohamintry-Study and teaching)

l,
Ye

f4
177'1-

X. vie 913)
.
'
ilo

87406
B/020/60/1.25/006/022/037
Bo16 Bo6o
AUTHORS3 Pereva7o,.raq E. G. IFeva, L4 P., and.33aukov,, Yu. I.
TITLE3 Direct Cyanation of Ferricininm Salts
PERIODICAM Doklady Akademil na,.ik- SSSR, 1960, vol. 135, Rc. 6,
pp. 1402-1405
TEXTs The authors report on ths-substitution of hydrogen atoms in ferzi-
cini", ferrichloride and ferricinium ferribromide. As had been expected;
the ferricinium cation was passive itt the electropbilic substitution,
since the-positive-charge, no matterm.whether localized on the iran atom
or distributed over the whole moieoixiev prevent's,electrophilic attacks.
Thus the authors did not sucosed in performing any electrophilic sub-
stitution in ferricinium. They there~tore attempted uuGleophilic sub-
stitution. Notable yields (over 50%) of n1trile of the ferrocene carbe-
xylia acid were obtained when using the solution of liquid NCR in anhydrous
tetrahydrofurane A yield over 80% was obtained when feTTicinium salt was
replaced by amixture of 11errocene and anhydrous FeCl 3& By this method
one may also obtain the hitherto undescribed nitriles of substituted
Card 1/4

Direct Cyanation of Ferricinium.Salts S1020160jI 35/006/022/037
B016/B060
(metbyl- and ethyl,,) forrocene carbo'yyllc acids. it waa observed from +Ihe
infraTed spectra of these nitriles fliat thoy contain a nonsubstit-ated
cyclopentadienyl ring. It was concluded that the nitrile group enters such
a ring as contains an electron dono.- subutituent. A nonsubstituted cyolo--
pentadienyl ring was missing in the other two compounds produced by the
authores in nitrile of-heteroannular-chloro ferrocene carboxylic acid and
in dinitrile of heteroannular ferroaan~i di carboxylic- acid. This was-
spectroscopically confirmed (Ref. 14),Electron. acceptor substituents
-efore believed to renier the cyanation of the cyclopen-ta-
(C1, CH) are thei .1
dienyl ring with which they are linked more difficult, the CN group ente-_z
the free ring. The authors doubt their original assumption of the ferri-
cinium oation being capable-of a nuclepphilic substitution, since the
effect of electron donor and electron :acceptcr substituents was found to
be as strong as In the electrophilic substitution, The material yielded by
their experiments is -regarded as being insluff-licient to establish the re-
action mechanism. The only certain fact is that the reaction does 13-ot begin
by an attack of the ON an.lon-against one of the carbon atoms of the cyclo-
pentadienyl rings. Two assumptions are put forth concirning -the reaction,
Meehanism- I
a bond is formed fir9f between the CN anion and the iron
Card 2/4

87406
Direct Cjanatlon of Fevricinfum Salta 8/020/60/135/006/022/027
B016/Bo6o
atom of the ferricinium cation, and the proton then attacks one of the
'hydrogen atoms of the cyclopentadlenyl*rIngs.. This hydrogen is split off
as a hydride compound and may be used up for the reduction of the ferri.
cinium cation, while GN binds with -the carbon atom of the cyclopentadienyl
ring. Possibly, all these stages take place simultaneously within one
single reaction complex (or a c7clio transitional stage). 2) There occurs
a specific electrophilic (or homolyti1c) substitution, and ferrocene and
CN+ cation (or CN* radical) are involvod in the reaction. In this case,
the role of the ferricinium cation (or of FeG1 ) 'Would consist in the
3
transformation of the CN anion into a t~ation (or into a radical). L. A.
Kazitayna Is thanked for having taken the spectra. A paper by Ye. M.
Shustorovich and fl. Ye. Dyatkina is mentioned (Ref. 8).
There are 17 referencesi IG Soviet, 4 M I Go=an, and 2 British.
ASSOCIATICN-. Moskovskiy gosudaratvenr~yy liniversitet im. M. V. Lomonosova
(Moscow StateUniversity imeni M. V. Lomonosov)
Card 3/4

3/062/62/000/010/002/003
B144/Bla6
'AUTHORS: Nesmeyanov, A N,j Petevalova, E, got Turlyeva, P.9 and
~Grandberg, X. I.
TI TLF.; Direct cyanidation of ferrocene derivatives
PERIODICAL: Akademiya nauk MR. Izvestiya. 'Otdeleniye khi.micheakikh
nauko no. 10, .1962, 1772,-11771
TEXT: Bromo, nitro, acetyl, phenyl, p-iaitrophenyl fe rrocenes (FI) and
phonyl ferrocenyl sulfone were cyanidatad;.ferricinium borofluoride (I)
aAd ferricinium chlorol-platinate (II) were spitheisized and I was
eyanidated. Bromo, phenyl,. and p-nitraphenyl-F1 were oyanidated by a
method given in Dokl. AN SSSR, 135, 1402 (1960).- The oyanidation of
phenyl-F1 yielded 88.5~ phenyl-ferrocene carbonic acid nitrile, C 17 H1.3 NFe,
.a reddiah-brown, oily substance with the composition G 71.06t 71-05;
H 4-971 5-00;g and 14 5.191 5-300. The, IR absorption'bands at 1004 and
1106 cm- I showed the homocyclic.atrual ure of thia nitrile. The substance
Iras converted into the amids~C 17H 15 NO,'ie by adding KOH and H2 2(yield 32~;
Card 1/3

S/00/62/000/010/002/003
Direct cyanidation of ferrocene... B1144/B186
m-P- 155#5 156.5 G), as it does not crystallize. A heterocyclic nitrilei
~c 11 UNFe waa,.obtained by cyanldating~.bromo_F' (yield. 701 m.p. 91-920ci
C 45.62, 45. .921 I'H 2.88g 3.091 Br 27.83p: 2T-167; H 5-00# 5#001 Fe 19,321
'19.46~.). Cyanidation of p-hitrophenyl..Fl. yielded dark redg.resin-like
'crystals of a heterocyclic nitrile, C I H 12 NO 27e, (m.p. 1341- 1350c; c.61.42,
61-40; H 3.55, 3.74; N 8.21p'8.37; Fe 16.54, 16-46%).,,,Cyanidation of
-only 3-and; 18% by heating for 2 and 6
nitro and acetyl-FI yielded .5 hrs,
respectively, even with a considerablet excess of-FeCl 3 and HCN. Treatment
of 1.5 g phenyl ferrocenyl sulfone wil ;h 4.6 g FeCl 3t 60 mg tatrahydrofuran,
and 3 ml liquid HCN, yielded 52~6 he-te-rocyclic phenyl sulfone ferrocenyl
carbonic acid nitrile, C NO S?e, (m-~P- 141- 141.5'C; C 58-30, 58-51;
17 2
H 3.38# 4.111 N 4.17# 4.39; 3 9.02, 9.131 Fe 15-97# 16.10~). Cyanidation
of FI-carbonic acid nitrile-with-a considerable excess of FeCl and HCN
3
added to it, increased the yield in dinitrile from 27 to 621~4. PI was
also cyanidated immediately into the dinitrile of 1,11-ferrocene dicarbonic
acid (yield: 68~6). Experiments withan equimolecular PI-mononitrile
mixture showed Ithat cyanidation into mononitriles is much easier than into
Card 2/3

s/o62/62/000/010/002/003*
-Direct cyanidaluion of ferrocene...
BUVB186-~
dinitriles. I was synthesi.zed by passing BF3-:thr ough.a. tenzene solution
of 5-58 9 F1 with 1.62 9 quinone. It is a dark violet crystalline
substance, C 10R10 BY4Fe, which is easily solu-ble.in H.20, acetone, and
-.nitromethane (C 44.06, 44-16; H 3-65t.,3-75; F 26-15,'28-43~)- II was
obtained from aqueous ferricinium ferrichloride solution and chlproplatinic
acidi.it is a bluish black, crystalline substance, (d H Fe) Ptcl which
10 10 2 6P
is moderately soluble in H20 and, when heated, decomposes into methanol
and nitromethane forming F, (C 30 39 30~ 221 H 2.77t 2.73; Cl 27-42, V_~
27-06%). When cyanidating I, 2(C Hj Pe BY +.HCN--*C H Fee H CH + Fe(C
2 4 5 5 5 4 5 92
+ 2HBF 44A of the initial compound.:wao, convorted into nitrile, and 45A
was reTuced into V.,
ASSOCIATION:
SUB.I,IITTL'D:
,dard 3/3
Moskovskiy gosudaretvannyy universitet im. M. V. Lomonosova
(Moucow State University imeni H. V. Lomonooov)
March 7, 1962

2/000/012/005/007-
_5/062/6
B117/BIOI
AUTEORSs Resmeyanov, As ~E., Perevalova'i, .9~ G., YurIyevg_t__b-,_2A.*_ and
,Dcni'sovich, L. 'I.
TITLEt Aeac'tion.between~ferrocene carb.oxylic acid nitrile with
organometallic compounds and'prod,uotion.of di- and triferro-..,,.
cenyl-methyl 'compounds
PERIODICALs Akademiya nauk SSSR. Izveatija. Otdeleniye khimichoskikh
nauk, no. 12t 196?p 2241-2243
TEXTs Reaction of ferrocene carboxylic acid nitrile with ethyl magnesium
bromide yielded propionyl forrocene 0-4-p- 38-3900) and the camo roaction
wit). methyl magnesium io6ide yielded abetyl ferrobene (mlIP-8-5-860C).
The.ketone y ield was found to be 70 and 80~ at a considerable Grignakd
reagent excess. Diferrocenyl ketone (m.p. 210-211OCi Yield 55-60~-) wac
obtained from reaction between forrocenyl lithium-and ferrocene carboxylic.
acid nitrile. Differrouenyl ketone 4as used for,syntliesizing compounds
of the triferrocenyl methane ucrius' not hitherto described. The reaction
of diferrocanyl ketone with.ferrocenyl lithium yielded 060~, , triferrocenyl
Card 1/ 2
----------

S/O~;2/62/000/012/005/007
Reaction between fdrrocene0,v., _B117/B101
carbinol C31H2 OFe3 U."P. 20 ~2050C (f'
4 rom benzene), molecular. weight 617.
It is a yeilovi crys-tallin.v substance showinG'in its, infrared spectrum a
5-556 om band, -c harac t cri s 1416 of the hydroxyl group, It J8 easily z;oluble
in-benzene and carbon-totachloride, poorly Soluble in other,and insoluble
in e thyl alcohol . If.cancentrated hydrochloric acidis added, it tt;,rns an
rr conyl carbinoll quite stable at room temperature, V
intense igreen. Tr,lfe 0
cha ges to a carmine-rud substence of unknown structure when heated in
benzene, malted or when chromatographed on Al 0~~overa long period.,
2
Triferrocenyl methane C P~ Fe (59~,) was synthesized by reducing triferro-
31 28 3
cenyl carbinol with zinc dust in acetic acid. It is a yellow infusible
cry3talline substance which-deGomposes at 20000.
~ASSOGIATION: Moskovskiy go'sudarstvannyy universitet il m. hl. V. Lom,-inosova
(Moscow, State v
University imeni )6. Lomonoso
SUBMITTED JulY 13 1962:'.
a d' 2/2
C
r

milt.
b,,,-, their IR absorption ap tatra.
MT-RM AN 88SA. Deki-gay. Vi 156, no. 4. 19A i 873416
TOM TAGS-, ferroceM, d,'-subs3titaited ferrotene, atvwture, IR spectrg., alkylferro-~.
cenyl=ide, PnCzqlg,--MCenyl=lAej pheAylfervewylaltrilso,
Gbzorptioup riagim.. la= r, .6vatial b1ndrancm, spectral
-IR eb-Orptl ij;ebtw6 6f -Ph
aml P-Ilqv3terrocanyir-itri-les war-- e--amined ';~,D dete=ine the structure Of tm
liomrz. Then~ are, allfff zvmre,3 In thti abF;-n.-PtAcm :Ln the 910-920 =--I ree4on La
and in pairs of dieub-
ntltut- I t -v%-~ ra b~j 1; am,-5rl Of dIff In ident-Ifin-ationa Im tlia regian,
a,a la~.4E.zudva :'r,-~querey and intaasity abzxwtAjx-jatjc of
Vie C-no fmd IM2 e-mup-8. !a tl2e 1;2-;LG=eri3 tbara mm diffaremen in tle 1600-1.700
Card

M666-65
ACCTZMM-.I ZIR., AS404U55
(K--H2) regions: the barA, for the defomed vibrations of
(C--O) and _UOO-3F'O
'n' litting if Ile bands
t
he y er.11tas ManiltaneouOq with a de-crewe 1n the up
:La ta~~ r' tf thin! N-- vllrat",.on~ ; the Bps--tra tmtsin absorption bands
for b~otb free wd 'n 1,3-ismers of met*Lftrracenylamide
=d phP-nvUe-xTGcewla2Djd5 '=-ere 1z' not s-'rplitting of the 44R2 bdad (!a ;,he corms-
pondiug ethyl derl vati,ra the aliebt D'plitting is explainea by the eff ect of the
et, nvllca-! no the azzile gro-m.). -'rbe ap~ctra of the 1,3-isO=rs Ix, CCI.4 are
swawnat similar to apectra of voj-u6~~" corres-poundir.6 1,11-ditrivativez;
they hava no bands char~gteriziag bonied wa-gmupa. ne isomers dlrj.'er In t-hc-
1AUngra intensity m~ W ~e The ethyl group Iii the ill
and !j3-Inogn6ra increaslis the iatec~ra-,I iata4slt son to th % C) th Un
U4..c= - t f e
flubatituted fe-rMceny1wLide. 1.4 the 112-lacm=,? atAbl-I t6d etbyl subsUituenta do
rea
"j;not - COWS-: tftio: InV- ae# appapp-atly due to load of cvn~ugpAicn of the anide group
I -Ath the eyelopentedlen t1 ring benausa~ "of 'a cee The e coualusiorls
14
J
kblmii prLTcduyMx)x-- wyedloWy AkrAcmii nauk WEIR
Card -
2/3

Nl~: kF 4-04 5 5
A,,adenq of Sciancei, SSSR).,
Imspit'ut a L&_mf~a trio rgani,_,hF~ t~'&L-h F Ak&-Ie%L-L
~.Tnst,.tute of-
ER, TZ,,F,, = Z 0a)~Feb64 IZCL: 00
01~4 Cm- M: 003

P7-4/1).r-4 /F' -4 R P L
AC( 1 S3 1014 :.',R C) 15 90 UP: ')0 2 6 S O(JO/X)5/0-907/0909
9 i ~-4 7. 13+54b. 7 2
A L, P,
jj~.C -V j, a p
h n
h,,)kava nc Pi65, '107 -14('9
T
TL -I] tde q v r t ~-;-q ti ~xy 1i c ic ron organic CO:TDOUrld
I? C J q y a na r. r r g -a n i c r) r c , c o I urw~ c h r av-- L o
g y
A 11 S F -A mix ,un, Of 1~eq :-jrenecarbo,-~y I ic ac ids , chta t -,ed b,
T-,~, t i e ny r r 0 n e w a v z U in the present of ~Ydr :,gen
p id fl D a m x u rr f e co r - pon"; :i,;, i-rldes , from whtcn rhe amiaps --f I , 2-
n ~n v e r r- c i~ c P e1 Wo~rE se.:)arated by chro-matogr i pl- y c,,a
t, mt P. g po t n t 9 , a nc~ a I u e i.
L-- -'T a r a b"! 1 a e~ the au,.iL i, kls~
~i ~i t tie a truc r-urf.. o f
w3'-4 ~-Jd .:f 'U'V, aa"~' ik ;3pr-c 1, rp and late on Lhe relatfve Idsor-, -
, I No Fe-i r~~c it~tv c-~-1:xamide waa found in t.ha teac, Lon

L ~ 1 i -; ~,-,-
ACCE~-S IC! A P 5,'-'! 15 5 0,01
-,I C whefi pheny ted, the n I trli I e group eniern
x ~A 8
ac I'd by ~he succasa-vz 4~:1,1-on of thionyl chlorid-e and arawnl-a:
0
Ij j. V
G
Nil,
p - " e-z C.-C any 1 berizam i d,, ('T,' ~,,--z t rum redox potential"; Jfffe-,
5 1 T nv, Ez' ~I '3f tt~e am-ides of -Oll-locellecarboxy lic acids. The. pro-
9,riit~'Iei3is is orig. art. haa: I table a-id
2 at.
AS CA elezmenroorg,a-iic: Foyedineriy A~zademii naLk S;-F,
t I 'D - '- a nrrne- f. a I I iC CO-zq,,C uad,5 AG4 (I i! -- o f Sc i enc e sS S SR
SUBM1,71 !-,T) 9.3 164 fx) SUB CODE:
NQ RE., ~.Yl iE R

L- 042-62-67 EWT(I)/EW,r(m)/EWP(j)/r/94P(k)/EWP(l) TJP(c) WG/R'1V/R'M
ACC NR, AP603bOiO SOURCE COM UR/0020/66/169/005/1083/1086
urlyevat L
JAUMUR: Dvoryantseva G. G.- Y P.; Portnova, S. L.; Stn~er, Yu;, N*.
Nesmeyanov, A. N. (Aca~e~mc
i0FG; Institute of Chemistry of Natural Ccmpounds, Acaden) of Sciences ;I (Institut
1knimil Prirodnykh soyedineniy Akademii r-kauk SSSR); Institute of Hetero-Organic Com- 1
pounds, Academy of Sciences SSSR (Institut elementoorganicheskikh soederiineniy Akade-
mii naux bbbx)
TITLE: Proton magnetic resonance spectra of disubstituted ferrocenes
SOURCE: AN SSSR. Doklady, v. 169, no. 5, 1966, 1083-1086
TOPICTAGS; proton resonance, ferrocene, analytic chemistry, spectrum analynis
ABSTRACT: The proton magnetic resonance spectra of 25 heteroannular disubstituted
ferrocenes with various substituents in both rings were taken and the rule of additi-
vity of chemical shifts of the ring protons was established. The structure of several
homoannular isometric amids of methyl- and ethylphenyl-ferr6cene carboxylic zicids and
nitriles of ethyl- and phenyl ferrocene carboxylic acids was defined on -the basis of
the PHR spectra. The PHR spectra were measured using 10% solutions in CV.14 and CDC13
and a JAMC-60 spectrometer with an operating frequency of 60 megacycles. In all canes
excellent agreement was observed between the experimentally determined chemical shifts
Card 1/2
UDC: 538.113t547.13t546.72

L ~ 042 62-67
for the ring protons and the chemical shifts calculated using the additivity rixle.
Orig. art. has: 2 tables.
SUB CODE: 07/ SLSH DATE: 1-')Feb66/ ORIG REF: 004/ OTH BEF: (03
Card 2/2 Ev

E I-; A c PC-4, ',--4.,/Ps-4
N-7,: ALP 3 0 15 5 9 1 J 00t, 2 5 1, 000 / 0 0 5 09 09 / 0 9 11
5,',,,-.13--:,4E-..72+c,43.422+537.561
A I -t i R A, N. Pereva izzlva-L P,
'111%rdviolet and vtaible, ablsorptioi
3 C. F I a in ho-roann''-, !,- r d i.,;,;b!3 ilt t.-! e rrocenes,
Va. ('14 -9),1
ro. 5, L9*15, 909
7' r-dox absorption spectrur~ ;;oix
nitr~le
AB'~ T C. -.7 :,.t- red-cNx potent,,41s were by oxidative potentiomet--ic i itra-
h i, 0-. -1 tile -mixture "W"') an,I were compared with va,( as
li k: ri r, i:z 4J I i Jev-'ations frolu addi A,.-i y
I-,
e me
D, '-,(v I - and pherivl-siibstitut ~c rzo-
F,-, n 7he e nn I na 1,)r. --D~ i-cox poz,-!ntials was shoun r b( a
v:v-.! ho- of of botwannuleir lioubst d I er-
u I Ell
-'r. W"I -it ~Ieaqt
-xie aubii- t-Lient ;fi conjuga:ed viLh the five-me-abefd
t:nd vij~iblc ab rbo:(y I I
aor-E)tio~i npecr-,u cof amidee of fqrroceneca
acti& -h~zl ~he abfiorpr4or, pepkT, altc):Let cotneide, butthe absorptto, irt en-

-rom one isnrnor
ty chang~-s another. As in the case of th,! re-
dox :)ot a the lowesc abso-pt ion ens Lt y, exhi-7)ited by the 6pectrum o : the
aci,_!, tadicares Ae presen of steric ~iin-
d arize Icatmed Dy Ll)t neighboring ethy", group) In the conjjillon etween thl~
a -iii d - gr~,,up and the f I've -membe ri!d a r o-m_i I C r III & , In contrast to ~he amide g--!)up,
t h t-- -, i t r 1 1 t- Z-; r ou p ha a a I ine a r .3 t r, ic t -,I,- , a nd, 1, 1, s cor, j u ga t ion w t t h t1fl. e a r ama - x
17 f rig 1 q ~Iul by tric rei.zhborin_G bulk-v nubscIt---aant; for this reason, I)
i~,pre( lei -It"Iev~nce-L Ar~: ~,-.),_nd -till
a of nLtrileB f isomeric met
acids, (_!-aa-.15 '.71 7ne SDectra if am-des of iso-a!ric
o - ~a-boyy,'r acl:,14 e Coap le~c and
.1 V . 4 C~ , . - - - ~ %n, _.'arround to another are mor
rzlquire inve6c i n7at torts. "We thanx L. S. Shilo-'Itseva fol providing thl-
v art. hAs: 1 tabla.
A _'~ S 0" 12- 1 -R i 'na-,ttiit ~ioye4inieniy Alwdemii nsuk ~Ssp
OT g AftOTNI ".9
Uc COrapo%indfi, Acadlimy of ScLencea,_SSSR)
r I) SUB CODE: OC
SUFRMTED: 2 9J u 1 (A
0 P, eff.-' S C. GO i-MVE'R: 0 5

-ACC NR, - AP7012431, ~ I I I
SOURCE CODE: UR/00621661000!,)08, 'z467; 14-6Y
AUTHOR: Nesmeyanov, A- N- Porevalova, E. G.;__Xur~yeyaq_L* P.*, GosteMcks 0- N#
ORG: Institute of Heteroorganic Compounds, AN SSSR (Institut elementoorganicheskikh
soyedinenly AN SSSR),
TITLE: Synthesis of nitrites of.phanylforrocenecarboxylic acids
SOURCE: AN SSSR. izvaqtiya* Serlya khimichoskay4, no, 8, 1966, 1467-1469
TOPIC TAGS: organic altrile compound, chemical separation, phany1ferrocenecarbowile
SUB CODEt 07
ABSTRACT: The authors dekribe- an improv:ei~ent on bLd method for separAt-
ing mixturar. of amides of-isomeric phenylferrocettecarboxylic acids, prepared by~,-
rro ell
the hydrolysis of the reaction products of the cyanation of phenyMi cen
The individual amides of the isomeric phenylferr c'enecarboxylic acids were con-i
vertea to the correspondbg nitriles. The nitrile of p-ferrocenylV-Snzoic acid
was also prepared from the amide of p-ferrocenylb--nzoic acid and used as a
standard in gas chromatographic analysis of the mixture of nitriles of 1,2-,
.,3-,, and 1pl'-pheny1ferrocenecarboxylic acids,; obtained in t-be c_winati f
ihd 'I I:aole*- LUPRS: 40
phquy1ferrocenee' Orig- art., hast-,-Z formulas' 22
UDC-.. 541.91,.542.951+621.785.666
-,.C.ard 73

i
Yur'-,eva.14
7i
-A
all 't I I of I
1 ia t i (:!.,i alkt,
V 3 1 i f- I'l V
iarated n
v

n e n v Ka.-k m 1 1 a -I e,
r, .1 -1 e L a Sciences M cl s K c; s,,
owjf-l(!!~ A"e 7-ily- Of
r. S, Ile
r7.
O, T I I E i -D

Tan years of cesarean sections, Akush. i gin. 32 no.4:39-37 JI-Ag 156
(HLRA 9:11)
1. 1z akuoherako-;ginakologichaskoy kliniki (zav. - profeasor S.B.
Atuta,
Golubchln) Dabarovokogo maditainakogo Inst
(GRARM 11 SECTION, statist.)

-i
AUT HTR5 Rempel!t S.I.p and YuOy'evaj L.V. 32-841/61
TITLE A Rethod for Determining Interphase Tensions, (Ketcd IssledeyvaniY'%
mezhfaznogo natywheniya)
FMIODICAL Zavodskaya Laboratoriya., 1957.s Volo 23., Hr 8., pp. 934 - 936 (USSR..),
A.%'* M C T For the meas-irement of surface terug1ons; on Vnes bovaylary between -
molten metal. and moliten salt (or arlag) X-ray radiation. may be usedp
but this is not possible in the case of molten Id,711t, metal- whose
derwity- little differs from the densibr, of their moltpn saltq. Reaearch
work-R- in this- field by A*N*Frumkins member of the Academy-,, (elsqtroo
capi-Mary cliznra),, as well as the works by S*V.Karpachfyv and &4, stromm
berg (electrocapi Uary- phenomena) are hero caUed "uninteresting" for
industry-*
This paper givema method for investigating the dependence of the in-
terphase tension on current density-s temperature and structure of the
electrolyte (or the slag) at high temperatures* A disk whirh is systemw-
, is fastened on the boundary betip3en the molten
tical.4 counterbalanced
.
metal and the electrolyte, By-a rod the disk Is connected with the
meaanring apparatus, The material of vhich the disk ls Lnad,~ ha,:~- to be
adapted to every individual case. For a magnesium mq'Ltj esgej a porcen
lair disk
, f astened to an iron rodo can be used, For alaninum in a
.
cryolit,o-alumina melt a dierk. of moltAn magnqalum oxide or stUcan. car-
Card 1/2 bide is, recommended. For measurements in the movable part of the appa-

A Method for Determining Interphase Tensions* 3Z-E~-21/61
ratus: the u" of an ion- or electron-tube with menhanical steering
ia provided. The paper gives a scheme of the propo!ied apparatus and
examples, of relevant research worfue (4 Mnatratiorm-)e
ASSOCIATION Foreat Eneineering Institute of the Uralo (Ura)!,#kV, 1-isotekbn1rh"kiy,,
institut)o
AVAILABLE Library of Gongressi,
Caz:d 2/2

YURIMO Boris NikolayeTicb- YUR'y MMTSOV, A.V.,
- ;_~~~~L31MYGVMj-C
retsenzent; SKO-ItOBOGACHZVA, A.P., red. i&i-va; FIATLid, R.M., tekbn.
red.
[Metbods of cajcu3.aUng.bIagt-furnace =eIting]'Hatody ranabsta domen-
noi plavk;~# Sverdlovsk, Goo. nauchno-tekbn. izd-vo lit-ry po chernot
J tovetnoi'metallurgUy 1961. 304 PS OPRA 34:8)
(Blast furnaces)

4i 'A ~ it V krImOir-, %J4 S =,;F-l P,,4 wdrv~.r
SALiNIKOV, V.V.; YURIYEVA, L.V.; MAKAROVAt F.H.; DRUYAN, Ye.k-
Regeneration of the cataly-tic properties of palladium black
in an-ultrasonic field. Izv.,vys..ucheb. zav.; khim. i khim.
tekh. 6 no.3:4,16-419 163. (MRA 16:8)
1, Ural'okly leaotekhnicheskiy institut, kafedra organicheskoy
i fizicheskoy khimii.
(Palladium catalysts)
(Ultrasonic waves-Industrial applications)

YURIYRVA, K,
157.
vatutino. Kast.ugi. 6 no.5:i6a-16d l'q
(Tatutino-Description)
(lam lo.?)

aM WAMM
YUR 110VA, M. X.: Motor Toob Sot (disc) "Frocluoing Cellulose :r.-cn hai*woo?,
bY the sulfite prooesavl. Leningxaa, 1%8, 13 pp Nin Higher msR, Lonin-
grad order of,Tenin Forestx7 Engineering Acad im S. M. Kirov), 1-1513 copies
(KL, No 4. 1959, lp-8)

X.P.; YURIYIIVA* H-K-. IKITIN,
TMTAYEVA, 44-- * -*~
jcAl conuosition of the pahuriAn larch
of the chem
Characteristics (KMA 11'.1-1)
L. Trudy InGto iesa, 45:22-30
wooi
(Larch) (wood-ChemintrY)

Nervous system complications, in antirabies inoculations,, Zdray. %deh.
6 no*6.
.32-35 '59- (KM 13;4)
1. Is Stalinabadekago Instituta epidemlologli i glglyeMr.

YMIYEVAN M.60
Provandofi of rabies.. Zdrav. Tadzh. 7 no. 3 46-4;7~ X749 160*
-(MIRA 14W

%I T
PRYIVAj- Ni. A.
Brain and its work. Kyiv, Vyd-vo Akademli nauk Ukrainslktii RSR, 10,51. 32 p.