SCIENTIFIC ABSTRACT YESAFOV, V.I. - YESAKOVA, R.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001962920002-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: March 15, 2001
• Sequence Number: 2
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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114411 kfati%kirf ill f1mi'll.1 11m.40'"m 14A 9. ;vmi Al 0
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cacbm with IrmJuptird doublit be", slid h, 14wim.
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wills. Hydirovabom deAlm with wpowed ifindsic brindo
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w1m. a# bisluvra ", The mWilvity Limits of the No-
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1% 44 thr tollry, whilt, h* noills. 64 SAW. hysirlmoube".1
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Wall; the samit remit was obWated wheme MvWCO w*4
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for dko" cA wemal aml twatichc4 x4rAcIam W thim are a**
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It 17J% of crude acuAkaes, cantMall of
C
thyi-l, didwl, b. It 1-1121- Ill" 0.75M, mV 1.4424,
and an a dd. sM. of rctl~ -wmc Awnw. Tin
t of Lhe - 104 reactim wax atba 4110011:1
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it d." 0.760. aV 1.4M. The kouctum of tU wmldl.
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0* irtvc4lon of ii(rtw(utC-% at the qUILIMIAry C StOol basting ft
00 gi jdauble bond, such mus in ofelins or its dienct. Tbc amt. of
such hydrocArImm-t in liquid-plume Lrackiaig ltimfucts k
00 %h4Mn IU hKIM-C With fi%ing b.p. 44 the firactiont. A
ms~wv file halogenation and hypaujitiltuation Of
00 tall is lw(4K*Cd ISOCIA1414111 10 Which the MOCCILAtillil
00 mol. is firo fixed to the double bond, then the atm*
sea bitinds are ckaved. And the hatogent are trandonned ftst* as*
Itaftj majemai: this esipuills the txmibdity wo the high
reaction fate of utch lukigras with other milerWi present
intherractirprimixt. Iviantylenr (1.011 g.) and RMUMS.
keftjqcnrftacikiavoithitxlittcno.t;)?"ctirmixkdiind4.70%3 gee
it. e4 life r-An, siva- treated (tw 0.5 fit. with 2.3 1. freshly U09
004
90%0 Iffelms. Cl Willer, AM llw fog, layer waf, iselill" WVUW W1411 coo
'Id "i1 NA49.. flik'l. anil isnalygird got Ci and ustdim.;
0011 197. a the i1mmy1cut Cliff not etecr Into n=ti=, thus 00,
Aj iihowing direct chlorination of imAiny1coft; extemom of
A
lL
the reaction to I hr. gave unreacted bominyleve. 600
71W suptm%ition that hypochkirittation is occompartled by coo
AAA
fumt chlorinat'w" L"I aho -led by the higher CI Coss-
tent than cakd. for all Im, giradict. Sc=t--. fee
UM
gee
04-2,0 htji. thoweil that SA-29X~ of trillat tailived at is, ve 0
for transfortrution into liar.. %9. Kosorm I
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Pmnyukova. J, APOW Chm. (111.9
(1945),-The oil from wds of L, ukixwa can be umul in
fonmuutbm C4 bish-r'nuit Irying vilv Among Ov vsm-
Stitucuts them w" wnd a ucw form of lin.;Uvi~ iwid,
whom kdjwbfvmid#, ai. 232-C. obtained by ctin. IA the
mj& belauumida with ether. G. %l.-K.tr"Ajx,*A
OCTALLUM"AL WCRAIW4 CLAW FWAT ON
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Ed 9;949M off ifissuhli; mr"etrt, I
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40, (111154 jovt14 Isil"Atily Ism trillp'. Idth is"Itisr 44 mpAilp folacts ill
IV 10
!
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.1wiff, h0mooftmons %t$0 1-4110 its Wi4i. 0U 4, 11 In Ifill
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~01111 fly IhAn lit lovit."CO, so 141 a. thr mailluil Ivactim is min. '?
fly
1*0 clornest, Arixuatic Gfirtard Ivagrut's f4low OtMind 1.4432 whik it do"Wrof sunt, a mit" I v 5,1 .
we too
ii, caurste of the reactions to a C"Ater evolut than He or Et Ifulf Plo-I.-AM,11 Adduct W 1114641 ,,
. : ills tuA15* . r,4vr a
0 'rignmol trolzointol. In mutfudkikon tit Kohler (CA' a, AS Wit, Coasts. 33.01~, Af, ("U"t-opts is to the asiduct
0 G 11,1111 v 0
00 -3 PC41). 194 1411h, (from 3.8 g. &tj moss! 31 C. Eliths) its 40 cc. cif the qIjuter or to Iso I-..0 V. I'VOIXIMOme In
V1.0 wisol Xi sovir (I It". r( - I V tit All C. 3-awthyt'l- 1011ce. RIM.C0*11 W -10" to -11% Milit(flklit (froxti a 4.
43 lei 111111 cv. lifill.). After warklag up Ai -it-- M11 olmt X14 g. IlIttlit) to #0 (v. 1410 omr-La sidyed linivir d 104. 000
so TtImml in C.A. JS, MKIA1. 62.91'~ to yicM. ulm dchyilmlimi as about, but at foskic"I 7 moo,
kepi4idoomr, dl* 11.77,10, at' 1.4441A was M-uttat distTi. ovcr Na. WO 11milly a
provourv. Knit toot.
ro 44) ji 4-osviern-34mv. Into 1711:?J11.~14 0~111441, alp &-nin. ovrr Na, 2.2 C, :+I,.j4-I,34rjeoBmw, b# 234-7 '. -00
. '11* 0
44", in 1W rv. WOO, vqo" to litmoIltor (tmm tht tu.1"r alshilitritle sioldret
1
lit [10 In a) cv. Kst.0 sea,$ A-Mvil "we 211") Solve it AS vill. quittgs. 40.9 AS.
11.5 G. Mg mad dO
it"; After StAtitfiltif UrVII'Might 4114141, dOCOMiM. With 1417111 211.11
0 fly Clow 10 K.
ext.. trillatclif mi krittissimi Alualam of friv-4titit
cm. dista. IN M Over 2 W. KH304 W4 a C. mmyd. CW4464 Go Immoyfoutso. VcrIc A. JJUkr Wkneral Momm
N4.*&, And flosAlly purifiled by rptirtlited olmn. tover Nat MIMI. htivh.). 1. Amo, CArms. Sar. 69, I;G"
this tdl'. it" 0.70-47. UM VIK4110 Of Cliff, h b-IJIMMI 1010 1 Intilt
jr&m; the fortfoscattism 0 1.) " 3.3 C. Tmakir Ara- fitilf-RoU (1) joust 2 sq. Al." at -34% fill assets fit rato thist Age
l'. hydritio. ht-Atcd tit to cc. Md'h its a malcoll toilat to f(W fba atliods - JERI if, nmil-5-tv, it" C.14.
pkift off its,
2(1 hm. gxve on owid formium an AN asit with 2-4. 74% Ag. jk451 urr rectwAvilif and ZW41 Of it hitalsol 011(wilk too
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a of, q 4-ft cc tt IS t to Itit still 4 1 0 no 0 #6 of I if N 0 a go-Ser ~f
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IWO-1 t-P. &s-1 qmmliv td catalpt. Atmit 45% W
11 Is mmtxwd of It" tv-
"cuk-t Is twiticqVultY With
A mrAU qtuatstity of tbt 3-t1 *ma, Thm wctt Wait-
fied by mc6in with thip Wgn&W magmt w4 tompoiwo
fnKTOM and *tivs. With knoon knimikh.
of the PhY%- rx
The int I frWOM of tk hightf4miging ritist. ON.
n
falimm =twowl chiefir 4 4K~Vl chb"Ivt 06-11 *"e
imp himber Metiff". At bishrr rcwomi frinpoi. and
whels inner ratillya wit *Md. Ifiv frAtIss"I W4L* 11"We svio.
14%; the witt, cd H th-t-tratni and the 1winwy #Atti,
Iwolut-I WAV CtMIMIM Witiciat extifely 40(o the MuTvASLA
mitiort; the quantity ill highimi-bouitts PCWIK-t abiduchl
the trutity 4A toovs-boili 9W-ccActkm
ft
prixtu"s bicimmm ftom a hV00W to a st"Itkut qt*Ln.
tity. 2.3-DiInCthYI-3-pCnt&*A IWO A PAtMjd*TffAdM.
tn. 49," Ad (tvin 4,4-diratthyl-2-Matatitif m. M-j
C. Wf%f
0 0 0 0 a a o 0 0 0 0 0 0 0 0-0 0 0 a 0 0 0 0 0 0 111 0 0 0 0 0 0 40
OL a 0-0 0-0 0 0 0 0-0 01 0, 0 0 0 0: 0 0. ~O 0 0 0 0 * m
00
0 41
so
00
00
09
0411
00
00
09
so
00
00
00
00
00
00
00
0 0 0 0 0 0 a 4) 0
0.0 0 a a 0 0 111 0

4
lie
ve
000
wwx
Cost
11 4: 4

oft Ifthmadoft Of the VW4 .tarl(w Hydr OCRIrum V.
i (in RUASIan.) V. 1. Eoafov. Zhurptal 0(johchei KAi_
a*-,3 inii (Journal of Ge6ffkl Chemistry), v. 17(19),
Aug. 1947, p. 1453-1447.
Prysents results of an experimental *nil thromd.
Cal vestiration of the bromination of mono- tind
!n
djo flnx a the aliphatic wries and of tho stnijility
of the products.
via wa
4.v oat
S.44
Alij __446052 .4
-ts to, 10 is M, too 4;
a LIP
WIF qv WIG 0 0 0 &-a 0_4b_Q_0 40 4p q1 so
At -Cis ; ,a I I-a 0 __ '
claw 1C.LTY
xt -1% so of to A P a a cl 3
00640
G 411 el'o 0 0) 0
M;W'O 0 04
j
4:041
"00
off
coo
4x 0 0
coo
&00
z*O
we*

ESSAFOV, V. 1.
"On the Attempt to Synthetize the Ketones of the Cyclopentene Series. IV
(P. 1518)
SO: Journal of General CheM13tT'.Y, (Zhurnal Obshchei Khimii),

xj~~/che-fia airy - B!"ne 87nthssis Jun ~ 49
chemi0try - G-rig=d React-ion
%g-ew"In ting ancl Iodinating H4'Dlene 1~ydro-
a&-bons Vith Conjuga-ta Do-dBlo Bl=ds,' V. 1.
lab of Org Chem, Ural State U,'!
ZZMsk, 14 pp
mr Obahch Vol Ito 6 - F-"Obtp
Far) W,11.
3-mathYloataaleae-2, 4; 2-tortiirv-butjyl-4J.
A 2, 3- 4-
... .... . ..
isiAnta ot 2, 6-d1=etbyloota&iene-4,6 are
LU aare prec-i", &..a yleld. of 2~
e Synthesia
_,p=E hemigqa-y Dien Tun 49
-4,L---)t-"IYlpecttuUene--I.,.3 la improved. Studies'
& redeticin of throo, fbUcving eystema:
4
.113 3-zetbYlhoptana-3-ou-5 and CZ~W~* (2)
criboa toridary alcohols, 2, 6-motbylo~tauv-:;
~-0-1-6 and 3, 4, 5-irimethylheptone-4-ol-3.
iftova that in the 464dration of4~, in the
Oik-tirateii tertdaty alcohols, baving
1*osenoe of carbinol the groups and C2
activity Is Oblefly cauml by the A-at=
Othyl. SWm-1 a 9 Sop 47.

C.4
The charactarladca of ale-wasstwated botmos, IV-4
V--I--FA-JUV. f- Gtll- CIMM. U-S-S-R- J9, 1100-1h
(1049)(Engi. trgmJAtloo).---Sm C.A. 44,5703a.
- E. J. V.

of 0.0-ita"ttirawd kowm, IV.
V- L RftfOV- ZANO. ObSkAell Nkin. (I. Gen. Chem.) 10,
31WO(INO); cf. C.A. 39, 91 8I.-Summarliat ion of the i
privious data (C.A. 33. 3Mt. 40, t4tys), 44, I(Iolb)
ah*" that the depre of conjugation of C:C and C:O
Unb &U. the reactivity of unsaid. ketones; iocreased
num ON R bound to the CO group decreases the extent of
owlagatitio. and the same takes ptwe with the R attached
totbe terminal C tif the C:C link, Two said. radiculs an
the letter C Atom decTe2ft the conjugation even more,
Md the action of a %fe-Et combination is greater than
that of di-Me at ---' Me And kri-Bu. Introductiozi of a
1~14. R on the 2n4 C Atom. with 2 radic*6 on the Ist C
atotti. givell the max. lowering of the conjugation. The
iodicatim cf tL- unsaid. ketones may serve to show the
SU'acturd types by incrmse of the Wine no. with inemAsed -
so. of dde chains from the C atom, of the conjugated
in, a '~tj I!n CC14 CAII Alto be used stmILU
tot
In. derrrtats urith an inm4q*d no.
of nulicals bound to tbt conjujultd system, The tipper
oceJuption licult to Sivtn toy vinyl littonu and the Ituver
Umit Iles with the rooropilp. Itavin; 2 quattroi4rit C atoim%
41thec:clink. Tlic koput-I 11*0 (the methoolsoftorrim.
win be give" in Lttr papet) wele: limlyluffam(flopir (1).
No 163-5% d:* 0331). Of 1.4124; I-slyhdrmetnethy? ethyl
kekw (0). by., 175-7*, d" O.M113. nt" 1.4471); balylidend-
welAQWtopyl helow (11f), forts IIU4* 114 O-PZ40 ~V mif
im
1.44 0;
MI, h" IM-10" 41,0- 0,M73. Ri~'
1.4480; ijoj=y4JrsrneLinr (V). lot., IN -h', d:* 0.347 .0.
XJ? 1.4w9; mesityl olkip IVD. t)r,i UN W* d" 0 8,;d.)
nV IAM; (VII), bns'164 d'*
0"1, V 1.44"1; (VMI.
bw 157-8 . d1o' OAZM. esir 1-411S;
he mo-2-ow RX),*b,. 1117-91'. dJ* 0.954.1, mi.' 1.44.151);
M, Imu 21Y.1 31,
0 0.11M. nAP 1.44411; licnitylieltnewrione IXI). In,
5
4 45'. and beasyWrilennithyl ttlivI kittitit (XII). in
40 The Inclination wai run by midn. of the ketont to
10 ~). EtOH, rinsing with 10 ml. MOILaddii. of 25 nil.
EtOll-Wine soln. und, alirr shAinit, 21A ml. 1W).

(0(10*W by 11141killit RILd letting stand 6 MfU. CC Woof.
Will titntiots of The etcen iodirse with wt&
III is ctled. from the reaction with 10 mi. 2% 910~ and a
2nd fivnUm with thioaWate, beoralwAtIous orwe 4ow in
CCI#. the lubta. allowd to $"ad 30 min. Alta mixing,
OW dw IIBC pnerated Caw. similarly flow the reaction
withmandictch. InAmIa.1pveankxfiwvo.oI3.S-
3.9 with 0.9-6, 117o III formistion, Whitt a 1370-ada. reft-
Um pve VA-M.2 antil MIA& resp.; U Its 5 tain.
pve 6.4-4.1 Mine no. and 3".31401 [it while Man
ado. Vtve 23.7-10.7 anti 07.3-78.817.. Wv.. hi I,, a tulm.
Ove 3444.2 &M JOZ~18.07.. resp. (tortm run oat
mittle); 11 in 5 * . pvc 3.1-3.0 ladift no. (HI not
While 1350 min. gave 15.1-18.6 and 133-
IM In 5 min. pvt 8.8-6.9 ant! 35.6-7116/0.
gap-; P" in 5 min. 3.24.5 kpdtm no. and a* HI
cited,-u . 1740 min.-gave-105.4 and 40.9% Hf._F"P.;
a &M a am. gave 4A--6.1 towne no. am au.1-44M-k Ki-
VU In S min. cave 36.0-4.6 wine no. and 92-".4
MuNk 17MIntin. pv* 136.7-3.5 and 50.2-66.0%. mp.;
VM to 5 mia. pvc 95.3-0.2 and W 0-6 441 White
In 1410 Mo. It pvw 1198.11-114.4 ' 'A'
IX In 5 min. pint IC9.7-5.7 wo 92,11-72311o. in
3 min. Vsve 3D.6-93 anxi 40.2-2.01%. . 71 .
tion cipts. pvc the following tm. Of gubwsUtutim
Md S&M.. Mg. - I 17-n and 194 -4. a 21-7 MW I
M 404 and 167-41: IV 17-14 ai;J 162-M. U -%an
161; IM 64 aM IM-6; VI 11-10 and 219-6* X 23-19
sall 114-16; VU 179-87 antl 119-141; VM 36-M and
19-18; IX 223-13 aM 50-64. The yl" of CIrlemard
rowlim with the ahm ketow, died (
dO.O. #A eba, al='d Vy It'.
the mults tattat bo taft pit
1111th w4 Slow IA4dft. is do pa"ek, dithavo tbd
GOMM11 hkAff rkib am xMoL wM #no= bilifug a
low degree with 1611,1walwev Iffliag mAde tor
t1W tam of Ittlalitatitin. V, V. L R#qFOv And V. V.
Sergo"Itars. DO. lidedeRvio"t (1) has
the highest detim of Conjuguloll ~ notate. In the RCII:
CHAc seeks, Le.. hocrease of R kuTexAft the indePrAdOnct
of the ethylene band. I does mot teact in aq. a1c. Sain.
with 0.1 N Iodine, Whitt Oith 02 ,y "n. the iodine 00. is
but IA7% of the"Y'. and e- a 0.5 V arjln. aims but
.2,W, Iodine Ito (a! theory), the butifidtfle ama?g tivro
and i71V~ .1 & thtorelical iodine no. -det
the *vnso 0004ftims. Hot of I &JO ffd Merco
and 700 of. 1.4% aq. SaUl'umted 'at 0' wil 121) .
AcH 11% 20 ad. 111.0. VC000011till to -2- Om 6 brO-- let
o gt&" "itraillbt at 01. atutrifirt(l with AcOH. will uld.
With NaCl gave on exta. swith Flo and ditin. in the
a crystal of Wille. I4,A7, 4 the product.
M.19-21 *, d$1 0 M14. RV 1.4319. firofnin-thm' -1 1
-at 0* in CCL ~10'98% of On theou-11021 uptake, rvvfl
wAh twice tbe theore4kul unt. at 11r; no IOU is evelytd.
G. M. Kosoiopoff

USM/ChemistU - A-1COhOI9 49
Synthesis
"The Synthesis of Tertiary Alcohols Using, Campbor
Aqe, I'll vy. 1. '-V'esafov, N. I. -Novikov,
Lsb- of Org Chem, Ur&I State U? Sverdlovak, (4 pp
"ZbAir Obeh-ch- EhLi-m" Vol =- No T
d of tert-lax-I me-thylb-orneo1j, synthesized by.
a n
In"tte-raction of campbr vp =6
high temperet-ares chiefly ecause of enol:Lza-
#- hp
Y" C=Tnp -'r- At 160C, enoll-zationn of camkthp.
7
1_11-accozDaw-Led by fbimasttbn of secon cu -.,
cout#lr-lng ca=z~hcr, latter reaction biing-chler
ceI yield of tertiary alcohol
of r. redu
2/50TV
Alcohols Jul 49'..
Synthesis. (Contd)
Iftet ayntbevie is carried out at -150 C. At,b4;h
4,
chief secondary reaction Is redue-
ttou of camphor into borneol. Submitted
29 Mar 48,

Charaterflation of m.11-ummitura0d ket;0":-im.
V. 9. EsaVjUral State Univ.. Svtrdkmkl. ZAmp.
ObykbrK lm~m. (I. Gen. Chem.) ZO, IWO-7(19W); cf.
C.A. 44, MI0d.-vrJt-Vnsatd, ketones with nornul
"Fucturr me more trAdily hydrolyzed mith 0.01 N thin
.ith 0.1 N NaOll; ketones similar to mesityll oxide be-
have in the reversemanner. SibeligradAllonotreavivily
way be uwd In the cbaracteritation of ketmes. Ketones
analogous to trialkylvinyl ketatte, i.e. R%C:CCOR, Rre
even more resistant to hydrolysis, In the Ist Wries
0,1-0.2-1. samples were heated In munpuls with JfjO, ().Of
~w OA N NaOli M ml.) 2 lits, at l(W. and the C1111
resction on 10-m1. aliquots uml as the relative measure ig
iodine cvmuinpt Ion. cmled. on the star t Ing rnalcti3l. Inn
2nd scrics the alk. Wine satn. was allowed to react with
the W-ml.aliquot for 15 sec., 1. 6, or 15 min. so 4-4 to give
a measure of the An. Amts. of the reacted ketnum. The
results follow. INCII:CHCONfe: in Itif) 01,331"; re-
acted, in 0.01 X NiOlf 93.9117a. in 0.1 X 73.5%. C61118-
CII:CIICO.Nfe,64.3.$IA,717117,,.reip. hiesity1mitle,
44.C.4, 75.43. 90.78%. EtChleX11CORt, VIZI, WAfl,
92.16%. EtC.Xfe:C]6feCOMe, 37.08. 31.0. 46.4411'0'.
71C Imtones with normal structure have a higher degree (4
conjuralion than acclum In branched-clumin analogs and
thi-o is held it) be the reason for their mogt easy cleavage.
#1 %1 V-1-fr

ak
use 61 tas, Wo(mm mcuan in the analysis of somt or-
k CNIPOW41., " V . I. V #A Io v tj I Id N . 'NI . ftlhv~ ;6 1 A . It,
lIff 00, StAt"06 ''''!WCAMMIA,
C
Aut. Aim. 61 11A ANXI11411). -Th't Woftwill traC11011,
i.e.. the reactkm tit ccmqodi. contS. the group or
CII.CM0111- with ' followed by ltyclrolygi-i and Mimi-
fialk of Cliff Was Imm. MAO with a,$-unwd. ketoste% wid
their timmpontlius krials 11.11 hAvi"t thr4r Xfoulm Ism ca-
rblejoi,yielcift Amaltichysle tw sattP. mribyl krimm 1110m)
avillt Irm, e.g., aml 4-morcer4i-
IHIV. mvffAwr the drill, Imi'M flit C1111 [Torthm 44 41,0-
111owid, 111okJ161011w,4 al"I fit lbell if kP1140 'Ally 11 111i'm
hVilr4il"It YkIll 2 iftl4c of ImId. ult-1110 6,11411. 1w ithif Ivilt
111111 itICINTI k0twe If I(Samitate. W 11-~Wh

~SSP,,;M-emietry - Diene Hydrocarbons Apr 52
--,rAtjon ard Iodoxidation of !,I-Dialkylbutadie-
,Sri-, 1.
Me-0-7 ~'
?art VIII"' V. 1. YeGafov, Dab of Org
Cb-em., Ur-II State U
*'%h-1Z.~: Obsh-ch KbAm" Vol XXII, No 4, pp 6o4-6il
of dialkyl allyl carbinols in presence
procc--~dr in 2 direetiu.-E vith the forma-
tA'c= of diene bydrocarbons both iilth bQ .-
4M;~ vith :4 canju8ated system of double bonds. Vhe-
vie~~4 or the 11;~tte-r is the !over, the lower tbr deg
cC tlyd-rogenation of the allrjl group to 4,Ite
c--'t4pol C-atom-s. In 1,1-dimet4lbutadiene-1,3., in
224T36-
c6nl-~t to dl-isoprophemyl and berxadieze-2,4 the dbu-
IbU -bonds are- less strongly conjugated, and the brami-
MUI -,m or iodotidatian proceeds more fuI3,Y. Tertlj:ary
ales vith an aLlvl radical split at the bond betvpeen
423-j-1 radical and the C-atom of the carbomyl radical.

UUFOV, V. 1.
Hols, of Russian chemists in developing methods of synthesis by
m4ane of zinc or&nto compounds. Trud,- In4t.1st.est.l. takh. val.6:
318-346 '55. ("M 9
(Zinc organic compounds)

IIPA. I T
T. ~.T~-
I A I ~ 11,

li-11 j-
IIE-

ILLU
RM

I i t . I : ! , *,, . i ii t, I 11m:
i ... h?, , k'-- 11: 41,11,1111111111 INI: 111 1h.11., I li"i. ~11;i
I ; I . I : :

YESAFOV, V.I.
Chemical structure of C H and synthesis of new -phanylated
12 14 1
diene (1,3) hydrocarbons. Part 7. Zhur.ob.khim,, 27 no.10:2667-2675
0 157. (MIRA 11:4)
1.Ural'skiy gosudarstvenny7 universitet.
(Chemical structure) (H7drocarbons)

AUTHOR: Yesafnv. V. 1. q

T! ME': investipal'icn of' tte Thermal Peecmpos;,L:t!,n 71"

1. On thp Ch~-r?-jstry of Oxoniu!n Compourt,J!3
(T, K kbimi4 oksoniyevykil snyedineniy)
PPMT,'A'rP~'! 7hurn!il -`~r-oanev K),..-mll, 195.8. Vol,~~ 28~ Nr 9~-
P P,~,
AMTRACT: Th,~ pver~,TO- investigation aimed at determining the
degrep of the binding stability of the 0.1hor mriltickilen of
.he w(in,ann,-d compoundsl for this n1so, th,~ method of
th,~zf-tialt &.tcmpnei~lon was used which h,3,t3 t,) bi- loreferred.
-'n ;n,? q-iven case to other purely cheirf7?-1 mF-thodci T a fi
fc-urd tn.-ts the ethers form dietherr wtth mi3pnep-Jurr,iodide
t~vrl rihim A-!vti f, viefor. binding of thf,. ivigne-o-im with tho
r,f tne etw:-., mol.eculeo whereby into
7.0 MPjrne.I~:.,jm lnti-,e3e and v"he r,
,qhowed 1;hav trie ethers wl*~h Capabi!.ity 1.~,
va-ic-,us kinas rF
Vard etnexe I,r.!.In oni-- the !.:.-,;M,iodide

Invi,-stip~atirr h-i Tri-rma, Tecompocition of Mr-.pr.P!7,. - un 7
Todidn,
!. On tiie (`heir.*~~,-., r-1: Compounds
eventhough -it vas formed-from magaesium. iodide
yipld!i rr,,4jrnwqLtw Jodide of
I I"f is obtwined of
roi i
the other ,) mixture of iodine rind mat,?ri_-:;[uin by
from
d-i ro'iacement -7,- th~, it ethew 'rom Mg,". V 11 V th e r c
--.1i lipht primary
nihorv wi it or ;;71., i .1 111,A).
dec,-jmuw,31t!cn of the magries.1% iodide dletller6 of the decon-d
ir 1- n ai,
10dide il, -o- etber,~l and ioA-ine
b, C'M t,~.-,,tct:Lons.. The secc-id
strorik4,jy hound to the mq-resium, It wal
flir"her ;3ho;qn that :.n.th!: thermal. I , _,rn -
he magnes-
of thp second kind w i ~ it ft i,;' Aiatic ethers
I!--- alkyls Oienoia and resinous form, One moiecill.e
fat, ether separates in free state, *he
Card 2/3 :,O~Iiv chemical bond of magnesium to the rxygen

T n ve 9 t 1 za n - F 1 h f ~ Th,~- rma I rics c a fn r, r) s i t i o n na p-i eri
lodi-i(.- "Lher'S.
On the:
of th
- -:., eUrt I.n rht- rnpi-neriinv iodide diether of
the wic.-or i p raves f tm. oxnnjum .j8tnvt,. Ir
fc,r !.vo decompmiltion W thil maqw,~,:um iodide diether
fir r.." #w: p.opr):f,!qj . Th", ZIA 1) fll! i%
A S 8 C, 0 1 i~'!N-a :!j,. ari n! f. v i I r ;,I e rv 1 t F. t
L9

FMM
AUTHOR: Yesafov, V. I.
TITLE: Investigation of the Thermal Decomposition of the Reaction
Products of Dioxane With Magnesium lodide-Diether Ua6nesium-
Iodide and the Mixture of Nagnesium, and Iodine (Izueheniye
termicheskogo razlozheniya produktov vzaimodaystviya dioksana
s diefiratom yodiatogo magniyap yodistym, magniyam i ameslyu
magniya a yodom )II. On the Chemistry of Oxonium Compounds
(II. K khimii oksoniyevykh soyedineniy)
PERIODICAL: Zhurnal Obahchey Khimii, 1958, Vola 28, Nr 5,
ppA 1218 - 1221 (USSR)
ABSTRACT: After it was found that ethers with magnesiur, iodide yield
compounds of the formula NgJ 2' 2ROR which on heating decompose
again to their initial products, it was of interest to in-
vestigate analogous compounds containing dioxane. Above all
it was found that in the action of dioxane on MgJ 2' 2(C2H5)0
and RMgHal.2(C2H 5)0 (Reference 2) a complete analogy exists.
The dioxaqe displaces equimolecul'arly the ethyl ether from
Ca--d 1/3 these compounds. Different from the ethers/the compound

79-26-5-16/69
Investigation of the Thermal Decomposition of the Reaction Products of
Dioxane With Magnesiur Iodide-Diether , 'Magnesiur Iodide and the 1.1,ixture of
Magnesium and Iodine . II. On the Chemistry of Oxonium Compounds
Mgj2 with di oxane, MgJ 2' 2C4H8021 on heating separates only
half of the dioxane contained in it, the other half auffering
decomposition. Thus the oxygen atoms of dioxane have a greater
capability to form oxonium salts than the ethers, and they
yield more stable oxonium compounds. The most typical oxonium
compound of dioxane in obtained in it:n reaction with a mix-
ture of magnesium and iodine. This product must be regarded
as oxonium salt of symmetrical (formula I) or asymmetrical
structure (II). The question if these salts form at the same
time, or if first salt (I) is formed which then converts to
salt (II) remains unsettled. It is only clear that in salt M
if it remains unchanged on heating the P,P'-diiodine-dievher
would have to be found among the docomposition-products, which
was not observed. The experimental results speak fully in
favor of structure (II). Among the decomposition products of
Card 2/3 this salt there were found: dioxane$ ethylene, ethylene iodide.

79-26-5-18/69
Investigation of the Thermal Decomposition of the Reaction Products of
Dioxane With Magnesium lodide-,DL ether j Magnesium Iodide and the Mixture of
Magnesium and Iodine. II. On the Chemistry of Oxonium. Compounds
ethyl iodide, acetic anhydride, iodine and mapesium. After
all zhe results of the reaction of dioxmne with the mixture
of magnesium and iodine prove that'the latter as well as the
ethers in this case do not react according to the scheme
C4H8O2+Ugj2___;:~C2H4J2+C2H 4Yg
as a high-melting dioxonium salt is formed here instead of
the low-melting ethylene Aadide. There are 2 Soviet references.
ASSOCIATION: Urallskiy gosudarstvenny universitet ( Ural' State University)
SUBMITTED: May 3, 1957
Card 3/3

i1gliff JM
5 (3) 3 07/7 9 -- 29 -20/6
AUTHORS: Yesafov-, V. I., Stashkov, L. I., Sirotlr-Ln,- L. 3.~
9u--v-d-r-ov-,--1-.L., Novikov~ Ye. 0.
TITLE: On the Characteriation of the %,P-Unnaturatod Xot3nes,. VII
(K kharakteristike a,0-nepredel'nykh ke"Yonov. VII)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, 1Tr 3, pp 845-849 (USSR)
ABSTRACT: The present paper is issued as firat publication of experimental
data on the hydrolytic cleavage of the aliphatic aromatic
agp-unsaturated ketones containing an aryl radical ahich :.s
directly combined with the carbonyl group. Ketcnes of this
type were obtained by dehydration of the P.--kotals which had
been synthesized according to the method of Grignardl- V. and
Colonge, I. (Ref 2).
CH3 H IT(CH CH
1 C6 5 3)Mgj
(CH ) C-Cmu 4 CH
3 3 3k;uAr
0M.
Experiments with respect to the hyd:rolytfc c1pavage of t1he
P-ketols were carried out as well. The data of table 2 show
Card 1/2 that the P-ket-ols are far more unstable than Lhe corresponding

SOV/79 - 2 9-3 - 20/6 -1
On the Characteristics of the a;P-UnBaturated KetorL-,iB. VII
ago-unsaturated ketones and prove to be more sensi'live to very
weak hydrolysis reagents. Besides, the behavior of the 0-ketols
in the hydrolysis differs from that of the a&-unsaturated
ketones by the fact that a change of the NaOH-concentratior,
exerts a slight influence upon the cleaYage intensity of the
P-ketols whereas the hydrolytic cleavage of the a,P-unsaturated
ketones is considerably influenced. The rate of hydrolysff.s of
the aliphatic aromatic ketones investigated increases signi-fi-.
cantly when the NaOH concentration is increaued from 0.01 to
0.1 n. 8 P-ketols hitherto unknown were syntliesized and dz--.
scribed. It was determined how far the hydro' "ytJ _- cleava-ge of
the 0-ketols and at the same tim. that 4)i thlb a,P--unsatnrated
katonon dovolopa and it waa provod Oiat the It~%Lor b,j"
little HBr on bromination. There are 2 tables and 4 refer(-.-.-.3es,
2 of which are Soviet.
ASSOCIATION: Urallskiy gosudarstvennyy universitet (Ural State Univ6raity)
SUBMITTED: February 18, 1958
Card 2/2

50)
AUTHOR: Yesafov, V. 1. 30r/79-29-7-5/83
TITLE: Synthesis of the Phenylated Lx,A-Uneaturated Alcohols and the
(1,3)-Diene Hydrocarbons.V1II (Sintez fenilirovannykh a,P-
-nepredellnykh spirtov i diyenovykh (1,3) ujrlevodorodov.VIII)
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 7, pp 2129-2132 kUSSR)
MTRAM In ordar to nolvo tho problomm oonoorti-Ent?, the oopi4rittion of
HOIAgX from the fording magnesium halido carbinolaten (Ref's 1-3),
the reaction of'2,2,3-trimethyl-5-p-arylpenten-3-ones-5
(Ar-C6H,, n= CHN H4, n-C 2H5U6H0 which may be present in cis-
and trans-forms with RMgX (Ref 4), are described here. The
experiments showed that among the three homologous ketones
2,2,5-trimeth3-1-5-p-tolylpenten-3-one-5 produces the best yields
in tertiary alcohols. These alcohols can be dehydrated only with
difficulties. In the Grignard reaction the other two ketones
mainly yiblded diene hydrocarbons 0,3)- This particular behpvior
might be explained also by the influence of a spatial factor.
The phenylated diene hydrocarbons (1,3) of the siructure (III)
and (IV) obtained show, compared to the similar aliphatic
Card 1/2 compound kV) ~Ref 3), a stronger stability of the double bond

IR "'LA1,19011, 19-1011WILUMIM1141111 1.16W41 .11A 1111 ui` 14161 '.W!Li.'.~ WON-A
Synthesis of the Phenylated a,~-Unsaturated 307/79-29-7-5/85
Alcohols and the (1,3) Diene Hydrocarbons. VIII
in pooition 3,4 and may be broininated t1iorerore only with the
separation of a high amount of HBr. The following ob,tlunaciturated
tertiary alcohols were newly synthesized and oharacterizedt.
2,2,3-trimethyl-5-P-tol.-flhexen,3-01-5 and 2,2,3-trimethyl-5-p-
-tolyihepten-3-ol-5 as well as the phenylated diene hydrocarbons
(1,3): 2-phenyl-4,5,:5-trimethylhexadienft-1,3 and 2-p-ethyl-
phenyl-4,5,5-trimethylhexadiene-1,3. it is assumed that the
stability of the halogen magnesium carbinolates formed by Grignard
reaction depends on a,A-unsaturated ketones. There are I table
and 4 Soviet references.
ASSOCIATION: Urallskiy gosudarstvennyy universitet (Ural state University)
SUBMiTTED. March 17, 195ts
Card 2/2
p
HIP

TAUFOV, V. I.
---------------
On the history of the origin of the stereocbealml. tbaery R%d
the attitude of A.R. Butler and some of his contemporary West
Xuropean chemists toward It. Trudy rnsta3t.eata tskh-3Ck-4-;-
135-174 160- (Stereochendstry) (MIRA 13:8)
. (Butlerov. Alexandr Mikhallovich, 1828-1886)

86499
S/079//60/030/011/004/026
B0011 /B066
AUTHORSs ly~ lsafov~,V- wI. and Yakunina, G. I.
TITLEs Chemistry of Onium. Compounds. III. Investigation of Thermal
Decomposition of the Reaction Products of Te'urahydrofuran,
a(-Methyl Furan, Pyrrole, Thlophene With (;he lUethorate of
Magnesium Iodide and With Magnesium lodide
PERIODICALs Zhurnal obshchey khimii, l1q,60, Vol- 30, No- 11,
pp. 3572-3576
TEXTt V. 1. Yesafov (Refs. 1,2) showed in his papers that the etherate
MgI2.2(C2H5)20 is a very convenient agent for the re4tive estimation of
the degree of aromaticity of the five-membered 0-, F- and S-heterocyclic
compounds. These heterocyclic compounds may be arranged in the followIng
order on the basis of increasing difficulty in the release of the un-
shared electron pair of heteroatoms with formation of "onium compounds";
and for silvan, pyrTole, and thiophene with respect to the degree of
stability increase of the electron iixti~t of heterocycles:
Card 1/4

86499
Chemistry of Onium Compounds. III. Inveetigatiod S1079J601030101110041026
of Thermal Decomposition of the Reaction BOOI/BO66
Products of Tetrahydrofuran, o(-Methyl Furanp Pyrrole, Thiophene With the
Dietherate of Magnesium Iodide and With Magnesium Iodide
This order is further.confirmed by the experimental data of thermal de-
composition of the reaction products of the mentioned heterocyclic com-
pounds with anhydrous magnesium iodide. Tetrahydrofuran forms with the
latter a compound which decomposes on heating by cleaving the hetero-
cycle (Ref- 5). Silvan and pyrrole give, only on heating with magnesium
iodide, compounds which decompose at high temperature, also under
cleavage of the heterocycles. Also on prolonged heating, thiophene does
not react with magnesium iodide. It follows from thin that furan and
pyrrolo, no woll. nn tholr nompoundal PlatntitIn t)l~ otnt'o of
"If"C'U'Unri In the heterocycloij only tit low temperaturesi, with increfloing
temperature, however, this state is diaturbedt in wh1oh connection the un-
shared electron pairs of oxygen and nitrogen are cot fron, and otable
onium compounds are formed with MgI:
Card 2/4

8649P
Chemistry of Onium Compoundsp IM Investidation 60/0)0/0100019
of Thermal Decomposition of the Reaction 06TSO"
Produaii bf'Totr&hydrofur&no4t-Hethy1 Favah, Py e MoOme With Us
Dietherate of Hagnf stun ladidq~' and With, M4V45E slide
[ Q'f-
Me. Nei
which also explains the gooompa'sition of 0- and on heating$
It was thus shtvn that i) tatrahydroturaft &Opf4dds ths diethyl other from
X912s* 2HO to-foft'Hj;ItM060 which t9 ddaaajorsA under oloaugs of a
Oplecule of totrahydraturano that 2) silyth am pyrrold displAdo one
196196ul~'Of'othir f,~dm R#1242(
029')iOp and Stye adaysun.ds yfth-HpZg w1itch
depom
.pope under cleavage of the heterocycles; thot )), 1hioghone roaotm
neither'with M42020235)20 nor with X6124 1 is Ansumad t at tho',
partioiYaiion of hoterostami In the formation of hotoid orgles inorls,166
their: - capability of forming anium denjoundso This &P~%uhption is oupported
by the fact that dioxano and to'trehydrofuran give,With 111Zg statlor!som-
pounds than simple aliphatio others# Oo Zo gusnotoovas So Ve 8011ALF1
Card 3/4

Chemistry of Onlux casymdeo We 14'reoUldflob Ofsa 010 0041026
of The=911doompisition of ths'laa4fign, 94,6 /011/,
'Oofy ~i
4
Oroductis of TotishydiWimat ct-mothyl ftrant Fjrzrdlzfp DiOPWRO ft'sh Us
Dletherate,of Napieflux Udid* ad With mspef4uo lodide
and Of So felU srs, thafted for xakinatmiutls ths NAMPLOSS. IMF$ aim
11 referenaess 5 fiavisto 4 No 2 British# SM 2 damuss-
ABOOCUUM gralf ekty sm"reftsusly U"Veslattot (1142 0$640
valverfiltyr
wi=*-=$ AuPst I So ~ 1959
ftr4t 414

IMT
YESAFOV V.I.
Characteristica of dletertl=7 ~-glycolv. Pal-t 1. 7,bu--.,,b.kbJm.
30 no.10:3272-3275 0 161* OMA 14:4)
1, Urallskiy gosudarstve=yy universitet.
~Glpols)

PHOW11111 ,W11 11;h; A
3 ?0
-,/190/62/004/006/002/026
P'l (11
AUTHOPS Tager, A., Suvorova, A. I., Goldyrev, L. N., Yesafov,
V. I., Berestova, V. L.
TITLE: Effect of the chemical structure of the plasticizer on the
vitrification temperature of polymers. I. Placticizinc of
polystyrene withdiphenic acid and naphthalic acid eaters
PERIODICAL: Vysokomolekulyarnyye soyedinaniya, v. 4, no. 6, 1962,
803-808
TEXT: Thermomechanical curves were plotted for p6lystyrene (Pst)
plasticized with 25 moleJ;o of: monomethyl-, monoeth-y'--, and monobutyl
diphonatei'dimethyl-, diethyl-', ethyl-butyl-, d-.*b-,;-y.-, ethyl-octyl-, and
dibut~l napi.,,halate. The
diheptyl diphenate; dimethyl, diethyl, and
synthesis of ethyl-butyl diphenate (b.p. 167-168 C/1.5 mm Hg, MR 91-69)
and of ethyl-octyl diphenate NR 110-57), now produced for the first time,
will be Dublished. The compatibility of the plasticizer with PSt was
studied on the basis of the critical mixing temperature, which lay at
100-1300C with diphenic acid monoester, below room temperature (sometimes
Card 1/2

.,,/62/CO4/006/CO2/C26
Effect of the cheirical structure ... ~'l o1 /.B1 10
at - -50 0C) witr- of t-his acid, and at room temperature with
naphthalates. ..Js-uilts: (1) The vitrification temperature, TV, of
plasticized PS-. drops with increasing compatibility. Pure
PSt had TV = 1050c, PSt with monoesters had TV . 40-700C, PSt with
diphenic acid diesters yielded the lowest TV. TV dropped with increasing
length of the alkyl radical: ethyl-octyl diphenate yielded TV = -110 C;
the naphthenates showed & low effect (TV . 9-480C). /2) With increasing
content o0 CH2
J. links in the alkyl radical, T of diphenic acid dieaters
approaches a minimum at n CH2 a 10-12, and then rises again. (3) The
structure of the aromatic radical of the plasticizer affects T :
diphenates (and phthalates) plasticize more intensively than n phthalates.
There are 3 figures and 2 tables.
ASSOCIATION:
SUBMITTED;
Card 2/2
'M.R~
Urallskiy Gosudarstvennyy universitet im. A. M. Gor1kogo
(Ural State University imeni A. M. Gor'kiy)
March 21, 1961

)P'277
s/iqq/62/004/GC06/003/026
Tager, 'Suvorova oldyrev, L. N., Yesafov, V. I.,
AUTHORS Topina,Ai. P. A I `G
T II'LE: Effect of the chemical structure and z'-ie si"e of ~he
plasticizer molecule o the vitrification trilmperature of
polymers. 11. Plasti~czing of pol:fmethyl methacrylate with
eaters of diphenic and naphthalic acids
PERIODICAL: Vysokomolekulyarnyye soyedineniya, v. 4, no,'. 6, 1962, Bog-a14
TEXT: Thermornechanical curves were plotted for polynethyl zethacrylate
(MU) plasticized with 25 rlole~a' of: monomethyl, monbethyl, and Monobutyl
diphenate; dimethyl, diethyl, ethyl-butyl, dibutyl, and diheptyl
diphenate; dimethyl, diethyl, and dil~utyl n' hthalato. 1110oults: (1) The
n
better the compatibility between polyner area plastic-4zer, the Greator the
drop in the vitrification temperature, T,,' of pure (TV . 1600C)..
(2) TV dropped with increasing length of the Ikyl radical3 of the
diphenate down to a --iinimum (-90C). (3) ,on esters of diphenic acid and
e
naphthalates showad a lower plasticizing effect (T.,,,%j50oC)- (4) The
Card 1/2

V
S/1qG/62/V-G4,/G-C6/GG3/026
Effec-. of the chemical structure ... B101/3110
struc-.~;re of the aromatic radical affoct!j the plauticizing effact. The
better Dlasticizing of dip~enates is explained by the ability of the
compo-~nu to be turned round the C-C bond between the two benzene rings. In
the cLie of monoesters, the free COOR reduces the compatibility. (5) The
molar concentration rule does not apply to the polymer plasticizer systems
investi,zated. There are 5 figures and 1 table.
ASSOCILITION: Urallskiy gosudarstvennyy universitet im. A. V.. Gorikogo
(Ural State University imeni A. M. GorIkiy)
SUBMITTEM: March 21, 1961
Card 2/2

USAFOV V. 1.
History of the discovery of organic reactl=s in the presence
of anhydrous aluminum halidese Tmdy luste lst.esti tWrho
39tlO4-3.40 ?62,, (MA 1612)
(11riedel-Grafts reaction)

V-ZA-VIOV) VILL SHITOV, G.P.
Characteristics of prirz-ry-tertiary IFI-93-Ytols, ;P(Lrt 3. Zhur.ob.-
khim. 32 no.9:2819-2822 S 162. (MMI, 15:9)
1, Urallskiy osudarstvennyy univeraiteto
~Glycols)

YESAFOV, V.I.; ZHUKOVA, L.P.
Characterist-Jes of secondary-tortiar-,It-gi7cciiq. J'art
Zhur.ob.khim. 32 no.9:2816-2819 S 162. (111W. 150)
1. Urallskiy gonudarstvennyy univorsitet.
(QIYOOlv)
i,

Y-,-,SAFOV,-V.1s; DASHKO, V.I;.; 1-11A.FLEX, E.M.
~l racterlstic,!j Bricondary-tt-rtinry J."'17cohn. Part
.b. Aim. 34 no.12:4094-4Cf,6 D 164 OIIMA -8*.-1)
1. Urallskiy gosudari3fvenn-.Ty universitet,
A NINTIMIRIMI 11111 Irilill 131i~l 1111iii' MiliAll H,7: 11: 111i1 H

1WR HwoAn and Anizal. Phyalology (Nor
mal and Patholaglcal.)6 T
Lymph Circulation.
Abe Jour :Ref Zhur - Biologiya, No 13, 1958, wo- 60370
Author :Yesakov, A. I.
Inst I "o -j"Ir-
Title Investigation of the "Automatic" Action of the Center
of IMhatic Hearts
Orig Pub Zh- obahch. biologii, 1957, 18~ No 3, 185-193
Abstract The contraction of the pooterior lMh hearto (M) in a
frog waa recorded on a kywgraph. The warming of the
spinal cord with a thermode on tho level of the III
vertebrum, produced an increaeo in the contraction rate;
the destruction of the cord on that level did not
interrupt the rhythmical action of' IR. It was stopped
only when the spinal cord was destroyed at the VII
vertebrum. The rhythmic activity of LH originates in the
Card 1/2

tl:i ti 0~ Z";
-)-t) (7:os i-:rd-.,r of I~ciAn .-.d C;rdpr o" -bor
V.Lm-,ono!7ov) CG- ic;:7

YESAKOV, A.I.
- ---------------
Metabolic factors of automation (exe=pl!Lfied bv the cerebrospinal
center of lymph hearts). Zhur.ob.biol. 20 no.1:28-34 --Ta-F '59-
(MIRA 12:2)
1. Kafedra fiziologii shivotn7kh Kookovakogo gonudaretvannogo
universiteta in, X.T.Lomonosova.
(L7MMTICS) (SPINAL CORD) (PHYSIOLOGICAL COHISTRT)

SNYAKIN#-F.G.2 prof.; YESAKCfVp A.I., kand.biologenaWc
Muncular sense. Zdorovle 7 no.9:9-10 S 16L (MiA 14:9)
(MCUIAR SEKSF,)

YESAKOV
Metabolic nature of the automatism of norva"ceLlz as r-Aemplifind
In the spinal center of the lymph heart,, Zhur. 6b. biol. 22 no.2:
136-143 Mr-Ap 161. . (19RA 14: 5)
1. Department of Animal Physiology, Staliw University of Moscow.
(HERVFS)

YESAKOV, A.I.
Problems of the efferent regulation of recoptoriv; baivod qn on
crxWlo of lingudl chtmrooptom Mulokall- M01. I t',Wl. .51 110.3:
.1-8 Mr 161. (MIRA .14: 5)
1. Iz laboratorii fiziologii i patologil. organov chuvst7 Nav. -
prof. P.G.Snyakin) Institute normallnoy i patalogicheskoy fiziologii
(dir. - deystvitellnyy chlen AMN SSSR V.V.Parin) ViN SSSR) Mo.skva.
Predstavlana deystvitel'stva chlenom Mill SSSR P.K.Anokhinym,
(RECEPTORS (NEUROLOGY)) (STORA.CH)
(TONGUE)

YESAKOV, A. I.
%thodology of neurodynamic investigations and practical work
1n the p~qeiology of hwmn anal7soro" brr P. 0. Makaravo Reviewed
by A. I. Boakov. Hauch. dokI. vys. shkoly; biol, nauki no-3:
208-209 162. (14IRA 15:7)
(SENSES AND SENSATION) (PHYSIOLOGY--LABORATORY MANUALS)
(MAKAROVS, P. 0.)
fl j.

MAKIN P. G. irof.; YESAKOV A. I. kand. biologicheskikh nauk
.4 js P
Our habits are stereotypes. Zdoravle 13 no.11:11-5 11 162.
rMIRA 15: 1-0)

YESAKOV, A.I.
Effect of the sympathetic nervous 13ystem on the olectric,
activity of tongue receptors* Tnidy Inst. norm* i pato fl-
ziol. AMN SSSR 6:63-65 162-2 (MIRA 1-1-.1)
1. laboratori-ya fiziologii i patologii organov chuvsts (zwro-
prof. P.G. Snyakin) Instituta normallnoy i patologicheskoy
fiziologii AMN SSSR.

YESAKOV _,A,I,; ZAYKO., N.S,
.t~~
Effect of guanidine on the functional activity of taste
receptoro. Fiziol. zhur. 49 no.8:984,.989 h- 163.
'114111A V: 2)
1. From the laboratory for Phyajology and Patbology of Sense
Organs, Instituto of Normal and Pathologio Phymiology,
U.S.S.R. Academy of Medical Sciences,, Moscow.

YESIKOV A.I.
Rcf1ax regulation of mapontanscuo" activit7 of tongim cheno-
receptors. Biul, ekop. biol. i med. 56 no.8:7-11 Ag '63.
(MIRA 17-7)
1. 1z laboratoril fiziologii. i patologli organcrv chuvatv (zav.
pof. P.G. Snyakim) Instituta normallnoy- i patclogicheskoy
fisiologii (dir. - deystvitellnyy chlen AW1 SSSR prof. V.V.
Parin) JW SSSR, Moskva. Predstavleno daystvitellnym ablenom
ARN SSSR P.K. AnokhirWme

YESAKOVO A.I.
Efferent reactions in the hypoglosaal ner7e. Kul. eksp. b1:2. i med.
56 no.11:15-18 0 [i.e. 11 ] 163. (MIRA 1?: 11)
1. 1z laboratorili fiziologli i patologii organoy aknivotv (zav. - prof.
F.G. Snyakin) Inst-4tuta normallnoy I patologiche3kay Viziologil (dir.-
doystvitellnyy chlen AMN SSSR prof. V.V. Parin) M01 SSSR, Moskva.

YE,SAKO V.. A. I
Mpu-tr.)ph~rsialog-ical nnalys!s of the functional =b-;1ity and of
processes rpgulating t~e tAsta rocitptor appovF3tus. 7~-udy Inst.
norm.1 pat.fiziol. AM SSSR 7:0-44 'C'A. (Ia-RA !8t6)
1. Laborstorlya fiziologill i patoiciii organav chu-istv (zav. -
p-,---l. P.G.Snyaidn) Initituta normsl noy i patologicheskay fiziclogii
s ss R.

YESAKOV, A.I. (Moskva)
Role of different regulation levels of recepto:-.3 in the
perception process. Vest. AMI SSSR 21 no.1:62-68 166.
OmA 19: 1)

YESAKOV A. .; FILIN, V.A.
L___j I
Physiological characteristics of the functioning of the taste
receptor apparatus. Fiziol. zhur. 50 no).2:269-3.76 F 164.
(MIRA 18:2)
1. Iaboratoriya, fiziologii i patologii organov d*tv Inatituta
normallnoy i patologicheskoy fiziologi-.1 AMN SSSR, 14oskva.

YESAKOV, A.I.
Pocsible specific stimulus of the llautomtic" center of the
heart. Biul. eksp. blol. i med. 57 n.o.6#19-22 Je 164,
(MIRA 18.-4)
1. Kafedra fiziologii zhivotnykh Moskovskogo, gosudarstvennooo
universiteta imeni Lomonosova.
-14
El.

MIYEV, YU.K.; BAZAH, V.I.; YESkF0VA,-AjLN -~-SELIVWWA,, S.31. AND CM0YAKH0VM, S.I.
"The Catalytic Transformations of Haterocyclical Compounds" ftrt XV1. "Syntbesis of
Certain Pyridine and Quinoline Derivatives of Pyrrolkine" Zhur Obohoh. Kh1m. 10$
No. 21; 1940. Moscow Order To Lenin State University imeni M.V.Lomonosova, Laboratory
of Organic Chemistry imeni Academician N. D. Zellns)4~,, Received 26 1%7 1940.
U-1612j, 3 Jan. 1952
''IA :, :, ~ 1 . 1 i i
!I i I!li:,, 1~ Fi 1 11111k1 1;11,;

YZSAKOV, I.Sq YASHCHNIIKO, Z.G.
Interpreting vertical electric sounding curves b7 the T method.
Razved. i prom. geofiz. no,30:50-54 '59. (1,aRA 12:12)
(Blectric prospecting)

U04; I. S.
YASHCMKO, Z.G..; TL
Use of electric prospecting in studylag the elastic properties
of Igneous rockso Razved.i prom.potive 110 23-29 '59.
(61, 13: W
(Rocks-41actria propertlos) (111astialty)

TISAKOV. V.A.
; ;nc~p.
N.S.Bodnarskii; obituary. lsv.Al SBISR Si9r.geog. no.1:0-96
Ja-F '54. (WLRA 7:2)
(Bodnarskii, Hitrofan Sterpanovich, 1870-1953)

USM/ Geagrai~hy Education
Card t 1/1 Pub.-45 - 8/20
Authors t Esakov,, V. As
t3 at Riassi n ti- e
Title : History of the origireation or geoeraphy. fjeultin a Ur .'r 17C tiet,
Abatract
Institution
Sifbiritted
Izv. All SSSR. Ser, gt,.Oga ~4' 51 -!60$' ;Julr;- Aligblit JJI:54
t History of the establIahm-at of geovmphy taeulties 3t qu-svim-l uni vei-s i ties
sirce the second h0f of tba 19th centurys
Acad. af Sc. USSR, Institute of Natiiral History, and T'achnique

rK 1% ~IM I
USSR dphysics Moscow University FD-1152
Card 1/1 Pub. 129-16/23
Author Yesakov, V. A.
Title the history geography In Moscow University (up to the establish-
ment of the chair of geography in M)
Periodical : Vest. Mask. un., Ser. fizikamat. i yeot. nauk,, 9, HO 7, 131-136, Oct 1954
Abstract : The Petersburg Academy of Sciences, founded in 1725, established in
1739 its Geographical Department. Th3 author lists the numerous studies
and expeditions undertaken after this date.
Institution :
Submitted : may 22, 1954
;' I I-;i-.. i~ -

YZSAKOT, V.A.; SO=IYET, A.I., redaktor; VOIDDIM, N.I., redaktor;
- - --MMMVAg T.A.,- tekbnlchpskiy redaktar
(D.N. Anuchin and foundation of the Ru0nian academic geoe
,Taphical
chool.] D.N. Anuchin I sondanie imenkal univermitetskoi googTafl-
heakoi shkoly. Mookva, Izd-vo Akademii nauk SSSR, 1955. 180 P.
:
(Anuchin, Dmitrii Hikolaevich. 1843-1923) (HLRA 8:10)

TESAKOV, V.A.
,- -,
M.I. Veniukov's correspondence with N.M. Przbevallskii.
Vop. ist.ent. I tekh. no.1:207-212 156. (WRA 9: 10)
(Veniukov, Mikhail Ivanovich, 1832-1901)
(Prshevel'skii, N.M.)

3(0)
SOV/10-59-3-21/32
AUTHOR: Yesakov, V.A.
TITLE: Scientific Contacts of A. Humboldt with Russian Scientists
PERIODICAL: Izvestiya Akademii nauk SSSR, Seriya geograficheskaya, 1959,
Nr 3, pp 124-130 (USSR)
ABSTRACT: This i1streview of scientific contacts of A. Humboldt with
Riissian s,;ientists. There is 1 photograph, and 16 referencesp
of which 15 are Russian and 3 German.
ASSOCIATION: Institut istorii yestestvoziianiya i tekhniki All SSSR (the
Historical Institute of the Science of Natural History and "Tech-
nology., AS USSR).
Card 1/1

X 30 11/ 1C-~5-9 -4-2t'3/29
AUTHOR: Yesakov, V.A,
TITLE: A. Humboldt's Anniversary in the USSR
PERIODICAL: Izvestiya Akademii nauk SSSR,, Seriya geoGraficheslcaya
1959, Nr 4, p 158 (USSR)
ABSTRACT: The article is concerned with the 100th anniversary
of the death of A.v. Humboldt; in the USSR. The
followinZ- personalities and organizations partici-
pated in the commemoration of the great German scien-
tist: Academician D.I. Shcherbakov, Cor:oespondin~;
,Tember AN SSSR (AS USSR)93.V. Kalesnik, Academ4cian
_
A.A. Gri.-or'-ev, Corresponding Uember AS UISSR ~.V
.
Obruchev, the Akademiya nauk SSSR (Academy of Sciences
USM, the Geograficheskoye c,bshchestvo SSSR (Geo-
0 CD
graphical "ociety M33R)t tho Glavnaya goo.rizj.o~lorvaya

observatoriZ-q im. A.I. Voyeykova tral GeoplWsical
(COZL U
Observatory imeni A.I, Voyeykov), the Astronomiches-
Card 1/3 kiy institut imeni P.K. Shtevnberrra (Inotitute o_f'
0

SOV/10-59-4 -28/2-0,
A. Humboldt's Anniversary in the USSR
Astronomy imeni P.K. Shte:cnbero), the Vsesoyu--noye
botaniches.zo-7 re obshchestvo (All-Union Botanical
;:)Ociety), the Otdeleniye Ire o loGo-,,je o6raf iche s'l,-likh nri~uk
(Section of Geolo3ical and Georsraphical I-31ciences)
AS U3SR, the Institut istorii yestestvoznaniya i tek-
hniki (Institute of 11isto:7 of the N,,:ttural Sciences
and Technology), the Sovet-skoye natsional'noye ob"-
yed-ineniye istcrikov yestostvoznnniya i tuek-lani-ki
(Soviet 11,ational Associatfon of 1Ustorians of IsTiatural
Sciences and Technology), the Moskovskiy gosudars-u-
vennyy universitet im. Uolf. Lomonosova (Moscow State
University imeni M.V. Lomonosov) the Moskovslroyo
obshchestvo ispytateley p:?irody ~Mosoow Socie'ty 01,
Naturalists), Obshchestvo sovetsko-Sermanskoy druz-
hby i nauchnykh svyazey (413oviet-German Society for
the Promotion of Friendsh-11p and Scientific Connec-
tions), the Gosudarstvenniry istoricheskiy muzey
Card 2/3 (O)tal;o 11ii0rical Museum), t1io Gw:ii.tdiivr;t;v(,,j1rVy jatl,,ey

-007/10-59-4-28/29
A. Humloold-bos -Anniversary in the USSR
izobrazitel'n,ykh isleiasstv (State Muse-un, of Graphic
Arts) , the IMuzey zem]_evedeniya IJGU (Geographical
Liuseum IT.,10). the Gosudarstvennoye- izdatel"stvo geo-
graficheskoy literatury (,")tate PublishinC House of
Geo-raphical Publications)and the Ministerstvo svyazi
SSSR (Ministry of Comminnio-ations USSR). There is
1 Soviet reference.
Card 3/3

YESAKOV; V.A.; SOLOVIYEV, A.I.j FEDOSEYEVO I.A.v otv* red*;
(Russian geographical explorations of Em-opean Russia and
the Urals in the 19th and the beginning of the 20th century]
Russkie geograficheskie iseledovaniia Evropeiskoi Rossii i
Urals. v XIX - nachale XX v. Moskva, Naukav 1964. 177 p.
(MIRA 17:11)

f. ";i 1. I.L i .1 R H I! Hi
.!=2 0 h R!""! 1R I H I mA
.......................... . . . ..... . .................... .... ..... .....-
NAUMOV, Guriy Vasillyevich; FEDOS=, LA.,, otv. red..LYFUA -
6" red.; SOLOVIYU, A.I.p red. 211,
(RuBaian geographical explorations in Siberia in the 19th
century) Rueskie geogreficheskie 'Looledovanlia Sibiri v
XIX - nachale XX v. Moskva, Nauka., 1965. 146 p.
(MIRA 19:1)

V.A.; PLAIUIOTNIK, A.F.,- ALEKMEV, A.I.; FED0,13FUl-W, I.ik.l
-
red.; SOLOVIYEV, A.I.p red.
(Russian ocean and sea studies In the Ic,-Lh to the bagJr-
ning of the 20th centurj) Rusokia okesnicheskie I morskle
iseledovaniia v XIX-nachale XX v. Mookvap Naukap 1964.
158 P- (m:111A vtl)

_USAXOV,_,Vasiliy Petrovich~ PARFENOV, Eduard Yevgenlyevichl
Pfld~oAd,v;, -V -n-tin Alekseyevichj LERNER, D.M,p rod,
(Automated electric drive systems with regulated semi-
conductor rectifieral SisterW avtomatizirovannogo olektro-
privoda s upravliaemymi polupi,ovodnikovyini vyprlaniteliami.
Leningrad,q 1964. 35 P. (MIRA 1731-1)

... if xLzhaner.
;~~1044A -, ,. i
- - X
Operating conditions of electric winchad on ships. Sudoetroania
23 no.3:34-35 Mr '57. (KIM 10:5)
(Winches) (Blectricity on ship*)

TESAKOV, T.P., kand.tekhn.nauk
Systems for electric propelling units usine, steady current. SudoBtroenie
25 no.2:31-34 F 159. (MIRA 12:4)
(Electricity an ships)
'A R~

L 33115-66
ACC NRl AP6024083 s6Wci--,-* d6bi. 6144/66/0001002/o235/o236
AlIT110RI Zav alov. A, Set Qjtlman As 421 gllchanov Ve Del Fams Mk lie I'll
hue-r--,
Ar,ranwovs Borger, Ae Yae; Greyor, Lo K.; Yi-s&--kov. V. Pd;
Yoe V.1
Vya-tman, Ko- I.; Abr7utin VO flaf-G-Ubanov. V. Vo; OfAChoMy, K*--17f--Yov0eYov, He Yell
-ffo-rUn-, ld-.-Efe; 6fW1Df1 V, Yoe IF.;, Avilov-Karn love go Net 1159usli, A. Gel
Bolyayov, I-* P.; Pokkor, I. 1-.F~
ORG: none,
TITIZ-s 0* Do Bron (on his 70th birUiday)
SOURCF-t MZ. Elektrono~hardka, no. 2. 1966, 235-236
TOPIC. TAGS: aloctric onginooring porsonnol, circuit breakor
AWITRACM Osip 13orioovich Bron uns born In 1896 in 1C.Untai. In 1920, hn griiehiabKl
from thn phynics-mth faculty of KharlkovTochnological Inotitooo . lie bocano a pro-
fosoor in 1930s He defended his doctorfs thosid"in 194& Dii~~ tho second world
var. ho was In. tho navye After don. o*AUrAtion in 199),. Enginoor Colonol Bron iront to
work towilii-nr, at the Lonin;Eed Indu4trial Corresp2ndonoe School* Ho bocamo tho head
of thn Chair of Thoo ical Puns of Slootrioal Tsahn4loa in lio in olow)ly
associatod with scientific and development work, and has cooporaktod closoly in thin
area with the Leningrad "Elektrosils" plant sInco 194de His work has boon in tho
reas of spark-daEsi~~~-~powr~M ;xsalwrti. Ho hsa published over 1110
M
entific works and 19 inventionso f5hpi
SUB CODEs 03, 09 SUBM DAM"
SOL)
J,

5.3300 77094
S0'1/62 -12 -_-rd/43
L
AUTHORS: Zhuze, T. P., Zhurba, A. S., Yesalcov, Ye, A.
TITLE: Brief' Commun icat tons. Investigation o7P-V-t7n1elation
and Phase Equilibrium in Ethylene-Cyclohexane Syi;tei.~i
PERIODICAL: Izvestiya AkademLl nauk. Ot~,ele~nLye IdiLmicheskikh nauk.,
1959, Nr 12, pp 2251-2253 (USSR)
ABSTRACT: Inve3tigation ol' binary- systems of unsaturated Ca.'302;
-and pavafflno, naplithenes, and avorilatic hydrocarbons,
pl'00010,13 pl',10tical intevest; 111 vl.,-!Vt of the 11ij,:h
oolUbi -a
lity 01' 'GhC1 1U01' III C0111pV(33!3(3d U1.3atAllat,ud (:-a;_,,cL;.
P-V-i;-I,l relationship of' the ethylene-cyclohexane -,ystem
was studied by the authors in a modified apparatu:3
described by Sage and Lacey (Trans. Amer. Inst. Minin
Met. Engrs.., 19110, Nr 136, P 138). Isotherms V -- 1'(p~t
were traced in the range from 30 to 1.500 for ethylorie-
cyclohexane mixtures with 20 to 85 molar, % ethylene, at
pressures ranging from 10 atm to pressures somewhat
above the saturation point of each mixture. Saturation
pressures and the corresponding specific volumes were
determined from these isotherms, and dew point pvessu-2es
Card l/N were established in a series of separate experiments.
A1 1111111!111111"111 IT

Brief Corr,,run.tcat;1c.;nL,,. Irive-st;igzitlon Of 7 7
P-V-t-11 Relation and Pha:jc., Equillbrium S ov/0, -
in Etliylei-if-,-Cyc!loiif-,YLtii,-~ Sy:;teiri
Data thtw obtained, served to i, race i5otherly,,.~
P :~ f(N)t (Villeve DT 113 the i!i,')Lar share of ut-hylene
dis.,,olved In cyclohexane); i.3othermla of t.`ie
con3tant fov ethylene anit K
isotheviiie; of' rno1ar volurtiu:j VM of the binary sy,5t(!m
Plotted ai.,;ainsl. molar, share 14 of ethylaric at 50 at.-~,.
2
In this mannev, the composition of' the coexistinE,
phases, the equilibrium cons*~anto of ethylene and
cyclohexarie at pressureo Lip 1,;o 100 atmand the riolar
volunic3 of mixtures at their saturation pressures,
were determined In the tenipevattire vange fron, 30
1250, Molar volume iaotherm,,3 at low temporatuves
were practically linear tip to N,) = 0 65; at hif,
-hor
te.irtp~~vatUre,,3, the molar volume fiicreaoc~.; oharply
St"IrLing N'.) = 0,50. There avc 3 fiCupes; and
3 rcf'erelicco, l-U.S., 2 Soviet- I.J..23. vor,,L-ence is:
B. H. Sapl*e. W. 11. Lacey, Tvunn. Amen,. Iriz;t. Milnin~;.
Card 2/N - w~t'. Engx.,. , .1-,6, 138 (.19110).
L
,4,

ZHUZE, T.P.; YUSHHEVICH G.N.,- USHAKOVA G.B.;,,,:(ZSAKOV Ye.A.
Critical parazetera for oil and oil-gas pystemEi, Reft.
khoz. 41 no.6.*25-31 Je 163. (MIRA 17:6)

AFANASIYEVA, V. B.; ESAKOVA, N. 11.
Relation between the snow cover and G. J. Wangeaheim's types
of circulation. Trudy GGO no.151:77-80 161jo (MIRA 17:7)
F I
A 11 1!R

ACCESSION NR: AT4046059 S/2531/64/000/166/0182/0188
AUTHOR: Yudin, M.L(Doctor of phyeico -mathematical sciencer,); Yesakova. N.
Afanas 1yeva, V. B.
TITLE: Preliminary evaluation of the prognostic significance *of the Information obtained,
from meteorological satellites
SOURCE: Leningrad. Glavnaya geofIzicheskaya observatoriya. Trudy*, no. 166, 1964.
Voprosy* interpretatsil daany*kh moteorologicheakildi sputnikov (Problems In the
of data of meteorological satellites), 182-188
IroPIC TAGS: meteorology, meteorological satellite, cloud, precipitation, weather
forecasting, long-range weather forecastfng, snow cover, radiation balance
t~BSTRACT:`The objective of this paper vras to develop a method for the preliminary
ch"acterization of anomalies of cloud co~rer, the radiation balance of the underlying
surface and the limits of snow and ice cover for subsequent use of such characteristics
i in long-range weather forecasting. The authors establish statistical relationships between'
such anomalies and the characteristics of future weather (temperature and precipitation);'
certain direct characteristics of atinospherio circulation are also anitlyzed In relation to
future weather. Determination of the characteristics of w-lomalles of the cloud cover,
Card 1/3

ACCESSION NR.- AT4046059
the boundaries of the snow and Ice cover and the radiation balance was done using mean
10-day values, for the period Septeinber-Nuvember 1948-1957. These values were
i mapped, after which the parameters characterizing the fields of individual elements
i were determined. The method used for constructing the maps and defining the character-
I Istics-of anomalies Is described briefly. The state of atmospheric circulation was deB-
cribed using the zonal Index devised by Ye. N. Blinova, the M. 1. Yudin meridional index
--and-the A. A.- Rozhdestvenskly hydrodynamic indices... These parameters were used
to-sUpplement the 10-day means of temperature and precipitation for an analysis of these
value- determined for a grid of points covering much of the European SSSR. Synchronous
P
j..statidtioal relationships werci established between the 10 mentioned parameters;
..,,a0hbhronoua prognostic rolationahIps also waro detormined. The ton considered para-
'iaeters,were correlated with temperature and precipitation for the 10 daya which fo I I owad.
-T~0-jcbmputations of the correlation coefficients were performed on a "Ural-111 electronic
I.-,2'q-9~iputer. Most of the results of the computations were plotted on maps, and 66 such
maps wore constructed. In a considerable number of cases relationships were discovered
which are characterized by quite high correlation, coefficients and with a stable Identical
AIN

ACCESSION NR: AT4046059
4 1 f 1:
sign for the entire considered area. It was found that dio selected parameters generally
give more information for prediction of temperature than for prediction of precipitation.
Ilowever, an absence of prognostic relationships to noted on a number of maps. The
method described made it possible to establish a number of parameters of the state of the
atmosphere and the underlying surface which are quite closely related to the characteristic
of future weather for 10 days In advance. The greater part of the parameters apply to
-cept by use bf meteorological -
those elements which cannot be determined globally ex
satellites. This emphasi;es the great importance of satellite obs rvations for long-range
forecasting. Orig. ait. has: 2 formulas, 6 figures and 1 table.
Glavnaya geofizichookaya observatoriya. Leningrad (Maia Geophysical
ASSOCIA710N.
Observatorv)
Ix

AFANASIYEVA, V.B.; YESAKOVA, U.P.
Statistical relations between the anomalies of cprt&ia
weather characteristics. Trudy GGO no.1653105-113 '64-
(MIRA 17:9)

AFAlT!':_!lYViA) "T.B.; Y2-,SJ!KCVA) Ila,
Re laticn of' t!~e !i !~_if t of the bowndar7 of sucw atner. tti t~e G,
I
~rangen,_-itilrr typas cf circulation 1,ti the flpring litiriod. Trudy r,00
no. 168; 45- 43 165,

MURI, YN,;AF,()VAy 11.1'. A 1-7% It! A3V
U ~ .. 4' L niffc~ince of
Prelizim-ry evaluatior cf tio preUncstic slt-
information returned by ineteorolo'gical satellites. 7:1-L,,dy
GGO no.166:182-188 t64.
(14TRA

Objective method for deterodnation of the lixting stage
of aelatin stock. R. Gorodets',:aya., 14. Sheremet, 11.
Shakhnazarova, D. Virnik, V. Smirnova, and R. Y~esakova.
Myasnaya Ind. S. S. S.R. 25, No. 5, 52-4(1954). -The
procedure for detg. the atatus of the Liming of gelatin stock is
based on extg. a s.,,-,nple and detg. extd. gelatin colorimetri-
cally by means of the biuret readtion. 'Results are given for
extractable gelatin in bome stock ah 5-day intervals for LjO
days of liming. Total extractablo gelatin is dotd. for vari-
ous bones and other gelatin stock.
M. M. Piskur

GORMMTMYA6, R.V., kandidat khimicheskikh umik; SUMMUROU, H-Sh.,
mladshly nauchnyy sotrudnik-; SIMRIMM'. N.V.; YIRIrII, D.I.;
SKIRNOTA, V-Te. ; UWMI, t%lxf-
Reducing losses in gelatin production. Trudy VIFIIHP no-7:108-113
'55. (nu 9: 8)
1. Voesoyasan nauchno-IssledovatellftLy Institut mysenoy promyohlen-
nosti (for GorodetskVs, Shakhaacarova. Sheremet); 2. Hookovakir
zhelatinowyy zavod (for Virnik, Smirnova, Yeaskova).
(Gelatin)

GORMTMU, R.V., kandidat khinichaskikh aaWc; SETAXNAZAR , M. Sh.
mladshly nauchan sotruftlk; SMUaM, N.V.; TIOU, D.I.;
SHIBOVA, V.Te.; YMKOTA, a.
Kethods of determining the degree of liming in galatigemous tissuos.
Trudy VNIZIM Ao.7:114-122 155. (KM 9 18)
1. Vaesoyuznyy nanchno-inaledovatellakly- institut myssnoy prorq-
shlonnosti (for GorodetskVa, SMkhnaxarove, Shertmet); 2. Modkov-
skly sholatinovyy savod (for Virnik, Smirnova, Yesakova).
(Gelating)