SCIENTIFIC ABSTRACT YERSHOV, V.V. - YERSHOV, V.Z.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001962910011-1
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: March 15, 2001
• Sequence Number: 11
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

L' WM6-6!(,
ACC M AFOOM49
of 6000 km. The oil cooling eyatem"wid memauring oqullne-af; elre~~ deac;titbed and a ftagi-m
is given showing j6fd-Cs of ij'a~zur~Fent. The oil templa-ratu .re 'Aliermcl-
l
couples mounted in the oil lines entering and leaving the engfrit.,i. T1.9j! re-ading,~ Vere
recordedby an automatic potentiometer. Provision was made for cont)-olling the flow o!
water and oil th-rough-the cooling. systeri ead for control-ling and mon.~toring the, oil
pressure. Results for the MM-468 ~~fteF-operating --- at 2200 r1p shcre an increase in
cheat transfer to the lubricating oil from,1250 Kcal/hr un.der Oling ~Ccfnditions to 1500
Keal/hr under full load, i. e. 20%. The corresponding inicredsei in guel consumption:wpu
frcut 2.0 kglhr under idling conditions to 6.4 kg/hr under full load, The relative head.
transfer, i. e. the ratio between the heat transferred to the.oil end the %total heat
generated during fuel c.ombustion, is reduced fraz 0.06 under Idling conditions to 0.02
under N11 load. The relative heat transfer for the ZIL-13G engine varies from 0.012
to 0.024. Thus the experimental results show that 1.2-2.5%,0).' the, hest generated
during fuel combustion is transferred to-the oil ia~automobllel engines under load. A
reduction from full load to idling conditions Increaves:.tbilri, ~~eat tritnafer to 4-6%.
TIds indicates that most of the heat transferred to, the: oil- bt due to friction. hbout
80% of the heat fr= gases in the combustion chadber is trainferred to the cooling syEs.
tem, and only 20% is' dissipated into the Ubric;atin'g oil. Tibia canponerit, represents
only 203-25% of the total heat transferred to the oll. or.fg.:~ art, has: 2 figures, I
table.' -- : .. r; .I- .
SUB CODE: 13, 21/ SUM DATLE; none/ ORIG FM?: .005
ca-d ~,jq afis

III-AII VA 1 311 JI H11111111 IVI'11111"
KATSNELOSON, R.S.;.YIMSHOV, V.V.
Studying the microflore of virgin and cultivated soils in the
Xorelina A.S.S.R. Report No.l: Microbiological characteristics Of
soils in the Karelian A.S.S.R. (with su6mary in English]. Hikro-
biologlia 26 no.4:468-476 Jl-Ag 157. (MIRA 19:12)
1. Inatitut biologii Karel'skogo filiala AN SSGR.
(BOIL. microbiology,
virgin & cultivated soils in Karelian ASSR (Rua))

Hilo, hll
KATMLISOW, R.S.; YERSHOVt V.V.
Studying the microflora of virgin and cultivnted solln of the
Karelian A.$ s R: Report 11o.2: Biologicnl acti'TitY Of goile in tbe
Knrelinn A.S:S:R with sunmPr7 in Znglishl. Milcrobialogiin 27
no.1:82-86 JEt-F '58. (MIRA 11:4)
1. Inatitut biologii Karel'skogo filiAla AN SSSR.
(KARELIA--SOILS--BACTERIOWGY) MUMS)

TYAGNY-RYADNO, M.G.; VIZIRs A.?;; I~V~V V ; SIN'XMKAYAP N-A..;
Prinizala uchastlyls FILMNOVAq N.A.
Microbicfenosis of the solls of win forest ~.ypcm in the mlivach"
Preserve. Trudy.KarIM.AH SSSR no.34*93-112 102. (MrFA 1631)
(gondopoga PAstrict-Soil micro-organielm)
(Kondopoga 4striot-Forest soils)

YE?sHOvq V.V.
D19tribution of a onifiera In ealls of main forest types it
the "Klvach" Preverve, Trudy Kar.fil.Ali SSSR noa34:147-154 162.
(',IaPA 16x1)
(Kondopo a Dtvtrint-4ollo-Baotoriology)
~=nif icAion)
17
F.

YERSHOVp V.V., kand.tekhn.nauk; SHVE7S,, V.V., inzh.
Development m1ning vith a large diameter borehole. Oor.zhur. noo
1261-62 D 63. (MIRA 17:3)
1. Institut gornogo dela im. A.A.Skoohinskogo.

ACCESSION NR: AP4043415
incompressible in the direction of the normal and that the tempera-
~ture varies linearly along the thickness of the layer. The Kirchhoff-~
OC~_~!s of preservation of normals is applied to
Love hypo the faces,
:and the Neyt (?) hypothesis of"stralpht sections" to the core. A basic
,system of differential equations for six unknown displacement com-
:ponents witli.boundary*conditions i& derived,by using Lagrangelt. varia-'
,tional priaciple. Orig, art, hast 35 formulas#
tABSOCIATION: None
iSUBMITTEDI 27Feb64 AID PRESSt 3088 ENCLi 00
.1SUB CODES AS No REP SOVI 002 OTHERS 000
:Card 2/2
:1

ACcrsSION NR: AP4043415 S/0147/64/000/003/0019/0028
PTHOR: Yershov Ut U 0
,TITLE: Equations for sandwich plates of varinble thickness
'S,OURCEt IVUZ. Aviatuionnayn toklinika, no, 3, 1964, 19-2B
TOPIC TAGS: sandwich plate, variable thickness sandwich plate,
.sandwich plate bending, sandwich plate buckling
'ABSTRACT: Sandwich plates with a core layer!of-variable thickness
rand face layers each. of which has a different but constant thickness ata.
tdiscussed. The flexuiii'and /'buckling, under normal loading; of a
!rectangular plate with core/and facos -nade of orthotropic materials
bare analyzed by conventiona:1 variatl,:jnaL-, methods taking account of
~the compressibility of thelcore. '.ne law of core-thickness variation'
js arbitrary but there is ~o-inVLal curvature in the middle surface,
-It is assumed that tha normal cjt~,ponent of the core deflection varies!
linearly ever its thi'ckness, that the material of the faces-is
tard 1/2

Rm
2-6~
ACC NROAP6018595 SOUR E!COD UR/Ci3'?9/(~t;/,002/002/022iO/O2lI
C B:
AUMOH: Pokhodenko, V, D.; rhiz~M, V. A.; Yershov. 1_yj
ORG: Institute of_Physical Chemistry im. L. V. Pisaizhevski AN IrkrISSR, Kiev
(Institut fizicheskoy khimii ALI UkrSSH)
TITLE: EPR spectra and behavior of subatituied indophenoJ-51 radi~&Is
SOURCE: TeoreticheskVa i eksperimentallneya khimiya,. v.~2~, no. 2j 1966, 24o-246
TOPIC TAGS: hindered phenol, oxidation inhibitort eltictrarA,!,rittrahiatlnr-stic resonance
ABSTMkOT: A study has been made of the EPR spectra and the~idtructure of nubstitated
(wM CH3s iso-C3H7, tert-C4H9, tert-051ill, ay;johexyl)~. ind43ih,enokir radicals
R8
R,
formed on oxidation of the indophenols. -IJ-is*~ -n-oted that hiildered~.phenols are widely
u-ed as oxidation inhibitorl3f-o-r-
po =ymersi It was found thitt the.1,Lmpaired electron

111HP 'Ywripup .. .....
j,29342-66
AP6018595
A-cc NR,
reacts with the nitrogen and vith the ortho and met& hydrogalls ov'boith benzene rinva
The reaction of indophenols with benzoyl peroxide to form indophedo:qf radica.1s, was
of the first order with respect to indophenol. The a=ihilation of indophenoxy radi-
cals in benzene was a second-order reaction wIth respeot to,-~the ritAlcal. From the
values of rate constants of the annihilation 6f radicals haVine (IJITerent 511bativuentol,
date, weve obtained on their stability. This stability dropped shfirply on going from
radicals vith o-tert-alkyl substituents to radicals with lasir,--bran6hed groups. Orig.
ext. has* 7 figures and 2 tables. Sm I
CODE: 07, 20 SWI DATE: 19Jtin65/ ORIG REP. 0061 1 (,19H RMF: 013/. ATD PRESS:
Card 2/2

J[ III
KUDRRI, A.N.; KOSTP A.N.;..YERSllMLll.Y,j TROSHINA., A.Ya.; POLYAKOVA, N.B.;
USPENSKIY., V.A.; TLRENTIYEV, P.B.; YAKOVLEVA, I.A.
Pharmacology of new P-dialkylamino ketones. Farm. i toks. 25 no.4:
437-444 R-Ag 162. (141PJ, 17: 10)
1. Kafedra farmakologii (zav. - prof. A.N. Kudrin) Ryazanskogo
meditainskogo instituta imani Pavlova i jaboratoriya apetsiall-
nogo organicheskogo sinteza (zav. - chlen-korrespondent AN SSSR
A.P. Terentlyev) Moskovakogo gosudarstvennogo universiteta imeni
Lomonosova.

LZUKA, R.Ya.; YERMV, V-V.; SHABAROV, Tu.S.
Synthesis of h7drocarbons. Part 41, Diisobutyl"etylana and diiiso&zyl
acetylene. Zhur.ob.khim. 2) no-7:1124-1128 J1 13). (HLRA 6-7)
(Acetylene derivatives)

KOST. A.N.; YMMHOV, V.V.
Reactions of h7drazine derivatives. Part 3. 3~-aryl-pyrazollaea.
Vest.Hosk. un.10 no.12:115-117 D '55, (ULDA 9:5)
1. Kafedra organicheakoy khImli.
(Hydrawtue) (Pyrazolins)

ivi- ~ ),!, #(
MgNTIYBV, A~P*; XOSTO A.N.; SALTYAKOVA, Yu.V.; TAMOVI VeTp , .,
~,
S.untheate with help of acrylic acld aitril. Part 29: Oyanoothylation
of sorp ketones. Pair. ob, kh1m, 26 noslos2q,2,54928 0 156.
(141RA Iliy)
1, Hookovskly Gosudarstvannyy iwiveraitet.
(Ethylation) (Katones)

P11 fill,
f b ri;
xvR.C-Z-q wylu
ft7LAr--aA-R- M- 27ml M." ~~, 'm. as I
41 !LM I
A111- Knit" Ir-
TT
'oil
-pill T-"
Oks
hit
i:A4 A0 a
R L11 A`L~4!
Mc
ULIN
If,. tit
tA
IQ:
:ij
U-j L~
F ;-~FAHAIJ

Ul J N
L L L

YERSHOVI V.V. Cand Chem Sci (dias) "Reactiono ofhactive amino
group# in the synthesis of pyrazolineall. Mos, 1957. 8 pp 22 cm
(Ylos State Univ im M.V. Lomonosov)t 100 copies (KLI 10-57, 102)

BMZ IN, V. 14. ;TUMMIROV, S.M. (br. 'Pladimix); VIKOLAY17, S.D.: GRITSYMC.
I.P., MIAZZ7, F.V. (g. Shakhty Khmenskoy oblasti); -BOCH&OV,
V.S.: YERSHOY. T.T.: SHUMILOV. D.
Useful advice. Fiz. v shkole 17 no.3:62-64 my-is '57.
(MMA 10t6)
1. Gorodskoy institut uao7orshenstvt;~antya uebiteiv, g. moskye,
(for Berazin). 2. Klyuchovelaya sentletnpya ohkola Saso7skogo
rayona, Fqrazanskoy oblasti (for Nikolayev). 3. 27-ya 91-kola, g.
Khereon (for Gritayuk). 4. Dokshukinskaya erednyara sh1cola
Kabardinakoy ASSR (for Boaharov). 5. 10-y& ahkola, g. Chelyabitsk
(for Yerabov). 6. Goroaskoy institut ueoverBhenatvovaniy& uchi-
"lay, g. Chelyabinsk (for Shumilo-t).
(Physics--.R"rimonte)
Hill i 11111! iI111.
I II H 11 IH il~ IN MII

488
AUTHMS: Yershov, V. V.; Kost, A. ff.; Terentyer, A. P,
TITLE: Reactions of Hydrazine Derivatives. Part 12. Reaction of Beta-
Dialkylamino-ketones with hydrazines (Reaktsii proizvodnykh
gidrazina. XII. Vzaimodeystviye beta-dialkilaminoketonov s
g1drazinom)
PERIODICAL: Zhurn&l Obahchey Khimii, 1957, Vol. 27, No. 1, pp. 258-261
(U.S.S.R.)
ABSTRACT: The reaction of hydrazim derivatives was eoctended to a number of
alkyl-aryl ketones for the purpose of investipting its rules and
to obtain pyrazolones W%ich cannot be obLained by any other method.
This reaction was found to be easily adaptable for beta-airdno-
propiophenones which have various substituentu in the nucleus and
in the alpha-carbon atom in the side chain. Xn this case the
reaction with hydrazine resulted in the formation of 3-aryl-4-
alkylpyrazolines. The presence of alkyl- or alkoky groups in the
A nucleus was not seen to affect the reaction processj the *lds
were high and decreased somewhat only in the presence of branching.
ca Card 1/2 The pyrazolines obtained from the hydrazine reaction, when exposed

THE
11; 1 li;iihil

qP

f ill

-EIMM~,

!i
i I ! .: ::! :1 1 . !. !
I -
! I I . :! , 1, 1!:l lcl~l"i 11 1
; i 1 1 i: I i Y 1 1111 mr! -; ;; 1

Al

1
NOR$
~
KOSTNA'N,, rzynisou.s.B. PA - 2714
O
0
1
,
4
:2 LZ
1 1-
-we S
1
L; of ;;;;sollu* Rings by the Aaylation.
1
W
Plasehhobelenlys Vivesolinevogo kolltea pri, atollirovanit' Ruel")
I
PRIZODICALs llokl'a"Y Akadeall Fauk HSBR, 1957t Vol 113, Itr 4# pp 813 - 816

13 ~R
,U
c;
veds 6 / 195T Reviewed# 7 / 195T
A33TRACT I IM* pyracollaosp which laak a oubstitutent an the nitrogen atom
qasp under the InfIlleaso of the aahydrides of acids or of chlorineg
be transformed lato corvespoadlag 1-mayliracolize. Howvverp acylation
As sometimes "onalcuso It was found to b6 posvible-to-direat re
action between beAsoyl chloride wid pymoOliuep according to their
Aonditionsp either la the dirtation.of a o'omplate dirruption of the
j azine-or in the
Wrocoline ring with fonwilon of d1boasoyl hydr
.
.41rection of a norsal.benscylatiosto It pyracoline Is-introduced
'Uto the abundance, of bevzoyl chloride in the presence of water
4U14, dibensoyl bydasla* aloas Is produaodo In the.case of an
XAY~rs* order of mixtures or of a ecuploto leek of walers benzov;-
pyjacoline alone Is produced. in the case of acetone usine the
reactioa is the sans.'ByLthe splitting of acetone azints acetone Is
Orodueedq which in Ideitifted-as.s, saslc4rb4zolo wherote from pyva-
9oline aesitylsze orAds'w" produie4p which was also tranctormed
into stilearbasole.. The ability of ;gracolize to disrupt the CH
Caft 1/2 binding corresponds to the arAlogous properties of ite structural

AUTHORS: Kost, A.11., Yershov, VV. N03cow) 74-27-4-3/8
,TITLE: Synthesis and Properties of Pyrazzolines (Sintez - svoy3t-4a
pimzolinov)
PERIODICAL: Uspekhi Khimii, 1958, Vol. 27, Nr 4, pp. 431-458 (USSR)
ABSTRACT: DurtIng recent years cyclic hydrazine derivativea bave been sub.-
particalarly Intense investigation. This inclules
jected to a
I
also the A --pyxwolints Yrith binary binding between the nitropn
atoms as well as the not su7Dstitutad A 2_pyrazolineq vith binary
binding between nit-rogen- and carbon atomv, and 1-aub,,3t'1.tW"ed
,n, 2-pyr-azolines. Thi present report deale especially with ni-
trogen-sub,stit-a-bed L2--pyrazolines: The mothod!i of aynxhetization,
the reaction of lWdrazines with unsataratea 0~-, P -aldehydt.,.q w.-.3
ketones, as P, 'r, - or r, S-unsaturated aldebydes ard ketone_~
under the influence of hydrazine produce oay hyar-azones and
azines. The report further deals with the reaotion of lhydrazllne5
with A-subst4t-atei ketones, witq the reaction of hydrazines ;nh
-halide ketones, -the reaction of hydrazines with A -aminok._
tones (in Which connection i-t mist be pointed out that recently
Card 113 varioas ~ -aminoketones, owing to the further development of -:he

Synthesia and Properties of Pyrazolines 74-27-4-3/8
Mannich reaction ( re&kt!q1ya Mannikha) ham-a been coanted among
easily accessible comporands). Uention is made of the works by
Nisbets (Ref 92), Babayan and Gambarywi (Ref 99), as well as by
Kost and Yershav. Thire follova a description of a compound of
aliphatic di&zoccopounas Trith pyrazolines which are formed ~by a
binary carbon-carbon linkage); furthemore, a 41escription. is gi~rlr.
of the "duction of nitrogen-oontaining compoux0s. The following
chapter deals with the production of pyrazolines from nitryllz
(action of aryl h7arazints upon unsaturated nitryls). There fol-,
lows a description of the properties of pyrazolines: of their ox_:~-
dation, reduction, alkylation, azylation And arylation. Moreover,
the decomposition of pyrazolines is discussed (reaction according
to Kizhner-) . In conclusion the report dea3z with pyrazoline-au"'.--
stituted comrNxunds: 4--bromopyrazoline easily separates the bromd_n-~-
hydrogen molecule (during boiling of the sodium acetate solution) .1
so that pyrazoles with a good yield are obtained. Further po_95~:':b:'~'11_
ities are mentioned as e.g. -that 5-nitropyrazolines separate ni-
trogentous acid, on which occasion pyrazoles are formed under tht~
effect of hydrochloric acid; it is further said that in 5-bromtrj-
5-nitropyrazolines nitropyrazol and In acid media bromopyrazol are
Card Z/3 formed under alkaline action. Further methods of obtaining

Synthesis and Properties of Pyrazolines 74-27-4-3/8
pyrazoline derivatives are described as e.g. from 3-nitropyrazo--
lines, 5-oxypyrazolines, 4-aminopyrazolines in cio form, 3-pyra-
zoline carboxylic acids. In oonclusion a short nurvey is given of
the physiological effect proauced by pyrazolines: A number of
1,5-diaryl-*ialkylamincethy*L-pyrazolines have analgesic proper-
ties; I-PhenYl-3-aminapyrazoline retards the growth of tubercle-9
(in dilution 1 : I million). The application of pyrazolines ana
their derivatives in pmctice has hitherto not had the attention
it deserves. There are 227 references, 50 of which are Soviet.
L Hydrazine-Synthesis
Card 3/3

XOST, A.N.; PERSHIN, KILOVANOTA. S.M.; YEMINOVA,
B.B.
Reactions of hydrazine derivatives. Part 23: 1-acylpyrazolines
and their action on pathogenic micro-organisms. Veat.Mouk.un.
Ser.mat., mekh., astron., fis., khin. 14 no.1:211-216 159-
(HHU 1318'0
1. 14%fedra organichaskoy khtinli t Voesoyuznyy nauchno-iseledovatell.-
ski khimiko-farmatsevticheskiy Institut im. S. Ordzhonikidze.
fPyrazoline) (Micro-organisms, -Pathogehic)

AU7-1'1.-(0RS: Kost, A. N., Konnova, Yu. V.,
Xershov, V. V., ?ukhadze, Ye. G.
TITLE: I'leactions of Hydrazine Derivati,.res (Reaktsii proizvodnyk1a
gidrazina). XXII. 3-Amino-l-aryl Pyrazolinas a-d *P~*.cir
Salicylal Derivatives MKII. 3-Amino-1-arilpirazoliny i ill-Ai
salitsilallnyye proizvodnyye)
PERIODICAL: Zhurral obshchley khimii, 1959, Val 29, Nr 2,
PP 498 - 5o2 (USSE)
ABST2ACT: It was demonstrated that 3-amino-1-phanyl py-azoline M.
ahich was synthesized by the authors alrcady earliL
1r, dispos2s,
like some other hydrazine derivatives, of a bactericidal
activity, that is to say, it inhibits t"-.e growth of t!.e
bacilli of human tuberculosis. For this reason the authore
synthesized according- to Duffin and Kendall (!'.ef 2) se--efal
3-amino-l-phenyl pyrazolines by reaction of PA~-unsaturated
nitriles with aryl hydrazines accord.ing to tl-,e oc-,~eme
mentioned. On the basis of some reactiono the affiliation
of the unsaturated nitrile apparently ta!':,:-~s place in the
first ntar!o of reaction, while cyclization occurs afterwards,
Card 1/3

Reactions of Hydrazine Derivatives. XXII. 7-Amizio_l-ar~yl S(jV/70-2q-2-2':;//7j
Pyrazolines and Their Salicylal Deri,,ratives
Only small amounts of unstable aminopyrazolines resulted
from the synthesis of Duffin ana Kof,dijil (Ref 2), which ,-,rtfj
carried out Btrictly according to slieriMoulioiic, [t
follovis that it is more favorable not t0 CIL:rry Out the
reaction in ethyl alcohol but in the hi,~;her boiling butyl
alcohol. Accordingly, godium butylate instead of sodium
ethylate was used as catalyst. Theoe modificationo of reaction
Pormitf.ed an increaco, in tho yiel(I of arrinopyrnzolint-,! by
20-4V,- (50-80',I/o of the th,,,oretical onc).3-amino-l-n-tolyI
pyrazoline (VI) was obtained by reaction of A-dimethyl-amino
propionitrilo Yrith n-tolyl hydra7ino. The most intej-.ce acti-
vity against bacilli was exhibited by 1-phc!nyl-'A-aminopyt!r_-
zoline (I), The 3-aminopyrazolinco 5~fithesizcd readily cit(3r
reaction with aalicYl-5-bromo salic~-! aLloh,, do and 2-oxy
naphthoic aldehyde under formation of briGht-col6red sLlic,'l
amines. Their absorption spectra are given in t"ie fiLure,
Almost all saalicyl aminopyrazolines r__ffor preci;;itations or
a -green coloration with salts of triva-lent iron; man, of them,
Card 2/3 produce characteristic precipitations iiith thr, salts

ezROP-ctiono of Hydruzine Derivativem.
Pyrazolines and T;heir Spalicylal Derivatives
+2 +2 +2 +2 +2 +2. , ~ro al-ow, 3 fii~llres
cu , Ili 0 CO , Zn , Pb , Be I'lic
and 6 reCereLices, '/ of which are Soviet.
ASSOCIATIOll: Moskovskiy 7osudarstvennyy universitet (Moscow S!~ate Uni-
versity)
SUBIJITJED: December 16, 1957
Card 3/3

IOW, A.R.. KUDRIH, A.R.; TWEBTITU, P.A.; YXHSHOV V V-'--
Hexamethylaninine kotonea. a now class of 100'al anostbetlea. vest.
Hook.un.Ser. 2: Xhim. 15 no.3;66-69 my-is 160. (MIRA 13:8)
1. Kafedra organichaskoy khimii t Wedra farmaVologii Ryasanskogo
meditainskago institata.
(letones) (Nexametbylenimine) (Anesthetics)
~ .: f , i - t

DOROGOCHINSKIY, A.Z.; NAKUPLTYANO L.A.; LAVRENTIM, VJ.; BOYKOVAI Ye.P.;
KOSTI A.N.; YERSHOV
I V.V!_
Antioxidant properties of some derivatives of pyrazoline. Izv.
vys.ucheb.zav.; neftli gaz 3 no.3;69-71 160, (KMA 14:10)
1. Ifookovskiy gosudarstvennyy universitet imemi 14.V.Lomonmova i
Groanonskiy nauchw-iasledovqtel'okiy neftyaroy institut.
(Pyrazolilie)

A. Z_ L A..

TIT Lr, 3~
!'ER I OD 1 CA I., j..hLkh 3-ft' I j~.. !,1t_
So. pp.

TEL?, 1. tT.4 of --'r

'
.- aa~
1
. I In Ih.tr c~pxz,
r
%;.
Ttv FYrl-l,n_
t, UC31 l:!rlre.t 10,.tit ... Is t t!-
~ll..I.l ..rv s5.tlh_t-I " PoAaml. -=ttItTr?"
Tb
f
I- I-rh4ayl zart~
:
b
ryratolins. pirazolino,
rt-il-5-thyl_
;jrr-lIrw. 7-p h b
l.k.5-tripL*nyt P7-.mm*'Itv.
c-d 1/3
of "-n" P.Tr-1in"

f
ttl., ryrulli-
In ~-Z. b. -C-round . or. ~btaa.ll fr- Cr.
r*spo=d%m4t rjrl~lz="t I -c%rb-l!--3-;h r.11 _d I
rrrr.11a. (R:r. 2). 3-aol,O -I
ph*
!
rrom, arylnlt~ilo, -4 Y_M!_
j
.-
1 114- -- -t-taln-d by Intors.%ion of binial a-41
I,;, fta lyljr_l...(~ 't Of tho, prop-I: On
wrawit..4 o,as el. co ;. 1't th-l~ hibt -, Ing fC.4t olth th,
sat
ch ..3 t.k-n .. a t.td.rd. .* -.11
ff
t! f ptra-v_, :!I h a
:
t
4
"
:
%
a t b %h. 4ff.-t of Is tyll" th M"' "p"'.
w
11
rt
of ~-a 3 ;or$ tsk-., tb-
"T -.-l & r a
'.1
lln 1.
f
p t
h g
I "
Tablo,"Z_VI- L - propar-A bj, r h
di.till.t r tt rsecrackIng And or Its temz*as 119"'In rr
o 'r
a ,-;.r.d t7 int.mi.ig in . r.-Io of
!,~; , a :s
th wsxql- .._ In4it1t.'I !,,y 7%rtcui '. th. fty of
30
I.:-%I- -to dd%tie_ ..?. 1. It. ~~-tr

ft-t of t.bility of ..Upl.s A srd B
Card 2/1
.-I ftrst. ?or thlo purpose th. sut"r~ 5tudiol ths Inhibil "I
'or ~ exid - `z" 1.
"s st"'Illy " stion by "t
rol""f -h* Lx4
lth_,z '
;
_.t.ftl
lhs"ll cis ofrOf.T 4039-Ae tr,)3T 4039
l
h.
I
l
T!
.;
.OtOr
f - so, do b,
'
;.
,
~
:
.
tI I - In I h:
:
.
,
th.t .00.
.Y"I
l In.d.rt IV Is' h.' ib~tttttc
.ffect t 't by th:
asxbauld o" prraz*llt-. In tb* 94-"p- Intl -Itb thly
..b.%"c
r.sLft* I. . ..n...ht,d I I L
I
I.
St
.,1 7
f.r.m...
r:j. -it.. Thor. art tabl.,
-
j
:
3 vI, n
.
'u . t
,n
r
yy
't~
j
..Mn
;
".roinyy Potralaum 1-vtit,sto)
3, 195P

c.rd

n, i
0 6, ,p -~-j Ki
o C~
IOIINQ~ el 0 0
0,N)
CQ
S>1

TO. Vl~
Sov,
S: Kost, A. N.,Suminov, I., Yershov,
FTLEJ.R-IS
TLE: Reactions of Hydrazine, Derivatives. )CKIIIII. C'yano-
ethylation of Pyrazolinei; With Acrylonltrilc3
PERIODICAL: Zhurnal obollchey Ichimil, 1960, Val '30, Nr 2,
pp 498-5oi (ussR)
ABSTRACT: Tile reaction between acrylonitrile and pyrazo-ILle in t`ie
presence of an aqueou2 solution of NH 4C1 was studied.
The.above reaction involve~3 the fl at N
Card I/it
j

s of Hydrazine Derivatives. XXVIII. VV37 8
SOV/7 9 - 30-2 -2
N
N
M R It 11 C 11,; 1 t I L 1).
I I ~) =,Hs = 11; ltlz- I'll,; It 1, 10~-
If - V ~, ;~, 11; It, -., It' :
(I V~ it ILI z~ It, ~ Its 1 11 : It- - kn -V,11-
It ILI It, 11 ; ILI It, .1
-C,11,;
I V1, 11 )it ILI It. 11 It, = C,J),.
(V 111 1, 1:411,; 1, 1, It' ~- It' - It.
There are 8 references, 7 Soviet, I Gemian.
ASSOCIATION: Moscow State Unive-mity (Moskovskly gosudarstvennyy
univer3ltet)
SUBMITTED: February 12, 1959
Card 2/4

Reactions of Hydrazine Derivatives. XXVIII. 77678
The obtained products and their properties are
below.
obtained Product bp/mm pr. yjald ri
D
I-A-cyanoethyl)-3,5,5-trimethyl 120-1210/ 1.4735 0.99A--
py oline M /10 71' 1
1-( -cyanoethyl)-5-methyl-3,5- 116-1190/3 14 1.4753 0.9586
dieghylpyrazoline (II)
1-( )3-cyanoethyl-li-ethyl- 121-1220/3 74.1 1.4'~43 o.956,[
5-propylpyrazoline (III)
1-()e-cyanoethyl)-4,4-dimethyl-5- 118-1190/6 59.3 1.4702 0.9422
isopropylpyrazoline (IV)
1-~e -cyanoethyl)-4-isoPrOPYI-5- .127-13o0/3 63.8 1.4703 O.W74
butylpyrazoline (V'j
Card 3/4

Reactions of Hydrazine Derivatives. XXVIII.
1-( ~-cyanoeth I)-5-phenyl- 175-i8o/8
pyrazoline (Vi~
1-( ~ -eyanoethyl)-3-phenyl- 195-205/11
py.-azoline (VII)
77878
SOV/~9-30-2-2- Ij
.~/7 3
v,4.8 1 -
70-4
Card 4/4

BOOI/Bo67
AUTHORS: Kost, A. X., Suminov, I0P qMjtullin B.,
Yershovp V. V.
TITLE- Reactions of Hydrazine Derivatives.XXIX.Cyanoethylation
of P-yrazolones
PERIODICAL: Zhurnal obahchey khimiit 19609 Vol- 309 No- 7,
pp. 2286 - 2291
TEXT: *The cyanoethylation of the pyrazoloneB has hitherto not been de-
scribed; there are even indications (Ref. 1) that 1-phenyl-3-methyl pyra-
zolone does not react with acrylic nitrile. The present. experiments how-
ever, show that pyrazoldnes readily add acrylic nitrilelin'the presence
of alkali lyes. To render the determination of the ture easier (ad-
dition to the hydroxyl group or methylene group in Position 4) pyra-
zolones were synthesized with a P-eyanoethyl group in position I or 4-
For synthesizing 1-(P-oyanoethyl)-pyrazolones-5 the reaction of P-hydra-
zine propionitrile was made with eaters of P-ketonic aoide. A German and
an American patent indicate that 3-methyl-l-(P-cyanoothyl)-pyrazolone-5
Card 113

Reactions of Hydrazine Derivatives.XXIX. S/079J60/030/007/012/020
Cyanoethylation of Pyrazolones BOOI/BO67
and 3-phenvl-l-(P-cyanoethyl)-pyrazolone-5 may be obtained by this meth-
od (Refs. 20). According to the data of the present paper the reaction
of P-hydrazine propionitrile~w_ith the eaters of various 0-ketonic acids
in alcohol, under short boiling, leads to the corresponding 1-(p-cyano-
ethyl)-314-dialkyl-pyrazolones---5 (65-W yield) (Scheme 1). The synthesis
of pyrazolones with the P-oyanoethyl group in Position 4 was based on
monocyanoethylated acetoacetic ester and the corresponding hydrazines
(Scheme 2). According to data by W. Kroho (Ref. 4) 3-methyl-pyrazolone-5
was reacted with O-chloro propionitrile in alkaline -medium under condi-
tions which permit a full enolization of pyrazolone (an equivalint amount
of sodium in tertiary butyl alcohol) with the formation of two products
(X) and (XI) which were separated by fractional crystallization. These
compounds had the same empirical formula which corresponds to the mono-
cyanoethylated product. With iron chloride they did not produce the
violet color characteristic of the enol form. They differed, however,
by their melting points and the solubility in water. A test melting of
a mixture of the two products showed no temperature depression. Com-
pounds (X) and (XI) show the same infrared spectra whose lines are
characteristic of CE-N and C - N (in the ring) whereas the lines of the
Card 2/3

.0I ~J-
Reactions of Hydrazine Derivatives.XXIX. B/079/60/030/007/012/020
Cyanoethylation of Pyrazolonea B0011boP
carbonyl group are lacking. On the basis-of these and further studies
the structure of the P-cyanoethyl ethers of 3-methyl-5-oxypyrazole
could be ascribed to compounds kX) and (XI), and their difference could
be explained by the presence of orystalline.modifications (Scheme 3).
There are 7 references: 2 Soviet, 2 USp and 3 German.
ASSOCIATION; Moakovskiy gosudarstvennyy univeraitet (Moscow State
Univeraity)
SUBMITTED: July 15j 1959
Card 3/3

I,, -
TMNTIT.U, A.P.; VIKTOROVA, Ye.A.; YBMISON. B.M.; XOST, A.#,;
Ms", T.T.
Inner.complex compounds as contact insecticides. Zhur.ob.
khtm. 30 n0-7:2422-2427 J1 160. (KM 13:7)
1. Mookovskiv gosudarstvennyy universitsto
(Complex compounds) (Insecticides)

V7
8107916C/0301008/002/o,a
AUTHOR31 Iro.t. A. R. T.r-t--, A.
TITLX: A441111, Of I -1' -1 Ph"ll 11 4r.,I.,Ito
?nl4DDZ=: Zb4 -4 'bob hey khISLI, 1960, Tol. 30, In- 0,
TIM rZrId1mv v-oL4 then )'"t*A Vith snilIDD in t~*
proe ban of mietallic aadi =d*r tte formattoz of 2-aethTI-5-~;-O~zZ L/
CIS3-yis-CU-m., . sasy~ -1, sis,il.r r.amt. -1
Occur, SIM Myl stitltsa, =-. -, =-- - &md
SI th p-cospo=48 ra"tAu more W.Lly. I 1" 7114 In
pr,044ot was o'", Sod with P~rhthjl =!to. it .- zot P.melbl. to
th; Ta &i.0 prad at -it7i dioalms. A dearv..~ ta the
tool
It7 0 th: union Snap "&.a.& the of VU-1.
card 114
..... .. ...
"Ph'"I an't", 0-n1truenill-9, dtftlo. .04tem-ides and phtbalini4e w. -T
set vitt, --TL241 pyrldizo, no roactim took plot. with ", p_jbyz
PYridinO used by the authom. War dId . rometta. take plat. vith ".:Z-
Scotto *star, othamaj. betka.1, Th-nol, and lcii" %I111fit.. A tl-
product I" a high uilirv
I to
-P-1 11 4":.Ik traCt.r.], ferauls 2) see ohoaj..4 sith p-tcl.1din.. ~-j,
stro= a d too proved, a) by the lacking 1-1 stmarptio. bmd la the
Infrar.4 s3.c%ruz, U) by the I.2-,o..tbIIIty of carrying out
fte I-wit"oo, compound vas, *k-laed fros, X with 00'. which conl't t.
reduced to the I-&.in* coapoma4 CS3C 333w-CzCR4-C6I 5 (3). C-7conet 3
1l2
we as* elt*lnfd by V~rvot odtLition of phonyl hydr.%i.. to Z-wst!tjI-5
-Y!41 pyrldimv. Corrss;,**AAW to a tjpLewl aryl hydrazint a
men% secardt t, ?I b tak I t I rc20box=*%:,un,4.r tb:,f.m.-
Una at 1- 1, -t.t ydr cart at* (4).
The ez"rizoattl part lints thh...yntbe.i. of the follo.ing c.tpcumls.
-"Lao@ tbjl) -pyridino I
cart 2/41
mominoothyl) -pyrl din*;
troto,.2-phanyl IoothJI)-;yTIdiaet 2-.. tbjrl - -Inv. ta:2)
I
,!rrIdIS4 and the roorso2tt'. I-acot1l ccapoundl th: torrompac, 1n4 - and
talylocaloo oamp.%ndst -Q.thyl-5.~2-0-ablwyla%in 0
tho respective and the corm.p.ndi.C p-antorl "ino
sout,vandal -Ito.thyI)-;rrId1aaj 2-.tbyl
(2-0-maPthyl &#Lnootby2)- yridinog salun-
taIX)-pyridinal
alrbasols. The asjority of the outstano 0 Ynthosized are highly 'I'-
san* *12m. Ezp.riments ms4v at the Intodrs, farmakologil Xlaakve~
uldittimakago L.otitut. (Cbir of Ptarmacol.gy of the Minsk
Institute) led to the fluding that part% .... I inj..tlon of the hydro-
chlorides of these companinds In It. leads to the ..ell.tlcmi of the
jarairapathatto nervous :jat;;O(=,vc;rIaw and nicotine offealt). The
11 axleity (LD,O,) Is t,.t.a an 00 *gAg live eight. I tmoo
groups In par& position Iner .. a the toxicity by Its lod-
a are more toxic then hydrochlorides. There are 4
r:thylat*n
foracom.
Card 3/4
10audarstvomyl ralvereltat (I
Vallor.ity)
SUMITUD: July 15, 1559

ZHIRYAKOV,, Viktor Georgiyovich; YFMHOV, V.V.,, red.; $HPAK, Y0469
tekbn. red.
(Organic chemistr7l organicheokaia kbimiiao Lllosk7av Gos.
naucbno-telvhn.. izd-vo khim. lit-ry, 1961. 380 P.
(VIIRA 15: 1)
(Chemistryo Organic)
~~ ; t, :I
~-l _;
~

YERSHOV, V.V.; VOLODIKIN, A.A.
4,Bromo-2, 6-di- tart. lzv.AN SSSR
Otd.khim,nauk no.0730 Ap 162o (XlRA 15SO
1. Institut kh W chaskoy fiziki AN SSSR.
(Cyclohexadionone)

UMHOV, V.V ; VOLOOKIN2 A*A-
Hindered phenols. Report No./+: Ibnnich reaction in the 2.,6-
dialkylphenol series. Izv.,AN 8SSR.Otd.khim.nauk n0.7:1290-1292
a 162. (Iff-BA 15:7)
1, Institut khimicheskoy fiziki AN WSR.
(]Phenol) (Mannich reaction)

VOLCLOYM: A.A.1 YERSHOV, V.V.
Hindered phenols. Report NO,5: Q~dnobenzilia rearramgewnt
of quinobromic compounds. Izv.AN SSSR.Otd.khJm.nauk no.,7:1292-
1295 j1 162. (MIRA 15:7)
L Institut khimicheakoy fizikt AN SM.
(Phenols) (Rearrangementa (Chexiistry))
jilli MWII

YFH,qHrJV,--V.V.; VOLODIKIN, A.A.; BOLDIN., A.A.
Sterically hindered phenols. Report No.2s SyntheBIB of
2,6-di-tert.amyl- and 2-tert.butyl-6-tert.anylphenols. Izv.11H
SSSR.Otd.khim.nauk no.6:1105-1107 162. (MIRA 15:8)
1. Institut khimichaskoy fiziki AN SSSR.
(Phenol) (Steric hindrance)

VOLODIKIN, A.A.; aRSHOV, II.V.
Sterlmlly hindered oberals. Rpnort Hoj: Phenol-dienone rearrange-
ment in the bromination of 2,4,6-*rialkylphanols. Izv.AN SSSR.-
Otd.khim.nauk no.6.1108-11U 162. (KRA 15:8)
1. Inntitut kUmichookoy fizAki AN SSSR.
(Phenol) (Bromination) (Rearrangomanto (Chom.lntry))

VOWDIKINY A.A.; YERSHOVp M.
Sterically hindered phanols. Report Hool: Synthaoia of isome
3,,5-ditert-butyl-4-oxybenzylamines. IzVs AN SSSA Otd.
khim.nauk- no.2:342-345 F 162. (MIRA 15:2)
1. Institut khimichealtoy hziki AN SSSR.
(Benzylamine)

SIXIFOROV.0 G.A.; DYUKAYLTO K.M.; VOL609-IN, A.A.; YkMSHOV, V-V.
Inhibitors of free radical reactions. Report,F#.3: Hbrvlation
of 2,6-dialkylphenolao Izv. AN SSSR.Otdokbimenauk no.10:1836-1838
0 162, (MIRA 15210)
1, Institut kbimicheskoy fiziki AN SSSR.
(Phenol) (Formylation) (Bgnza2dehyde)
3R-

IZMHOVP V,V.; VOLODIKINp A.A.; NIKIFOROVY G.A.; DYMAYEV, LIL
Sterical2y hindered phenolso Report NO-6-- BrOmLmt:t--)n Of 2,,6-
dialkyl-p-cresole and 3j,,0-dialkYl-4-h7&oxvbenzOrl bromiden. Izvo
AN SSSR.OtiWim,nauk no.10:1839-1843 0 162. (miu 1-~:10)
1. Inistitut lehimicheakoy fisiU AN SSSR*
(Cresol) (Bromination) (Reawangownts (ChemistrY))

.YMSHOVI T-T-0 VOLODIKIN, A.A.
i
Sterically hindered phevolao Report Noe7s NacbmIm of the
formation of bromoquinone compounds* Izv,AN SSSR. Otdokhime
nauk no.3.1&2015-2022 B 162* (MIRA 15:12)
1. Inotitut khimicheekoy fiaiki AV SSSR*
(Phenol) Ormination) (Steric hindrgince)

VOWDIKIN, A.A.; YWHOV; V.V~
I
SterIcally hindered phemolos Report gooft Fb=ticu of cyclo-
hazadienonea in the bromimation of 2#6-dI,*&IkyIpbenols, Im
AN SSSR, W.khimnauk no.11#2022-2026 11 162o (ND-A 15112)
1. Uatitat, kbimicheskoy fiziki AN SSS&
(Cyolobexadionome) (Phenol) Ormination)

MSHD71, V*W; VOLODIMp A'*~L
StarlcaUy hindered phomolso Report T**94 Effept of acid rsaMts
on bromoquinone acmpounda* lzv. AN &M Otdlddn.anuk rloXA2026-
2031 N 062, (mrPA 3.5m)
1. lwtitdtj~~cheskoy fisiki, AN SM
Nuum) (MMBOMWC ACID)

-'ilk 13 IIUIIW 4.114.M."W""! 1
BOGDANOV,, G. N.,--TEMQTv V. V.
Steridalir hindered phenols. Reporf,No, 10: Oxidation of
phenols by lead tatraacetate, lzv. AN SSSR W. kbim. nauk
no.12.-2145-2150 D 162. (MIM 16: 1)
1. Letitut khimichaskoy fiziki AN SSSR.
(Pbenola) (Oxidation) (Staric hindrance)

YERSHOY V. V.; VOLODININ,, Ad. A.
Sterical3,r hindered phanols. %port No. III Aetlou of'bromine
oz_2v6-diallql-4-etbylphsnd'ls. Isv, AN SSSR Otd. khi-u. nauk
no,121k504154 D 162, (MIRA 161l)
1. Institut khimioheekoy fisiki AN SSSR.
(Phenol) (Bromine) (Steric hindrance)
hid I

ff 61TdMU'MI.~..~i.]-.i..--l
XMINO A.H.; KOSTV A.N.; p~!I!p V.V.
Amin ketones intensifying trophle processem in the organism#
Vest. Hook, uno Sere 6: Biol.p pochv. 17 no,3:26-32 My-Je 162.
(MU 15:6)
1. Kafedra organichaskoy khiTnii Moskovskogo universiteta i
Ryazanskiy maditsinakiy iwtitut imeni I.P. Favlova.
(NETOMM-PHYSIOLOGICAL EMGT)

SHOPENAKH, Anatoliy Ernestovich; I&RSHOV, V.V red - ALAVERDov,
Ya.G., red.izd-va; HURASHOVA, V.I.-;-i:i;;.,r,ed.
(organic chemistry) Organicheskaia khimiia; dlia atudentov
meditsinskikh institutov. Monkvap Vysshaia shkola, 1963.
337 p. (MIRA 17:2)

VOLODIKIM, A. A.-, YMHOV, V. V.
Sterically hindered phenols. Report No. 12: DibxvmodIal)qI-
cyelohexadienones. Izv. AN SSSR, Otd. khim. nauk no.1:152-157
163, (MIU 16t 3.)
1. Institut khimicheakoy fisiki, AN SSSR.
(Phenol) 07clohezadisnone)
(Steric hindrance)

YMHOV, V. V.; BOGDANOV, G. N.; VOLODIKINO A. A.
Sterical3y hindered pbenols. Report No. 133. Reaction of 2 6-
di-tert-butybenzoqainone with organamagnesium compoluids, izv*
AN SSSR. Otd. kbim. nauk no.123-57-161 163.
(MIRA 1611)
1. Institut khimicheekay fiziki AN SSSR.
(Benzoqanone) (Magnesium organic compounds)
(S*Aric hindrance)
P Wit., I
i 17,1.11M

YRRSHOV,'V.V.; VOLODIKIN, A.A.
Sterically, hin4ered phenols. Report No. 14: Effect of p-substitnnta
in 296-di-tert-butylphenols on the formation of bromocyclohexadienones.
Izv.AN SSSR Otd.khim.nauk no.5:893-899 My 163. (MIRA 16:8)
1. Institut khimicheskoy fiaiki AN SSSR~
(Phenol) (Cyclohexadienone) (Substitution (Ch=istry))

L 12726--'-13 -TFF(C)ATr,7(m-)/BDS l>r-4 M11fd
LCCESSION liTt-, AP3002290 S too 621,1631/01110 1006f1l, 0 84 1---(J, PPI
AU11HOR: Bozdanov, G. N.; Yorph ~V~ I -I., ~,-
TITLE: StericallZr-hindered phen.als. Report 15. Syntlie-sis ol' para-sub:F~tituted
2,6-di-tertiary butyl phenols
SOURCE: AN SSSR. Izv. Otdeleniye khimicheskikli nai*, ao. 6, 1563, 10P-1-101%
TOPIG UGS: 5terically-hindered phanols. an "ixidant, v:rntbimis
piien I
ABSTMOT.- A method for synUicizizing Z,6-dj-+Axt~JaL- I Z) S
t,-- z
based on reduction of the appropriate phamal Ath lithi%m alli.Jilm= hydrl
-worked out. 7.hus, buty-1-4-methyl-~ -; ,`-5'~
tolvl-; and -4-Alplia--naphtlWl- phen.ols wGrs p,.,eT'lnvSA. lbeil,
dantleffectiveness was found. to be about 3/4 that of lrwrwj:~
thanills to Y. 11. Em~?.,iyizol for (!Orll)tqrlt intAwafit in 1;ho wal-l-, 3:1-1~
or-ig. art. IL A,-:L.
utlon." tzble, 1. 11gu."e, and 1. foivr
ASSOCIATION: Instit-ut khimidbaskoy, fizik1l, Altademil mallh.,
cal- Physics. AcadMy of Sciences SSSR)
Card

BOGDANOVq G.N.- YERSHOV V V
Nov stable phenW radicals. Izv,AN SS&.,Ser.khtW, nr,.8.*1526-1518
Ag 163. (MA 160)
1. Institut khimichaskoy fiziki AN SSSR.
(Phenwq group)

YERSHOVV V.V.; ZLOBINAp G.A.
Formation of nitrocyclobAxadienones by the nitration of
2,4,6-trialkyl phenols. Izv. AN SS~R. Ser.khim. na.9:1667-1669
S 163. (MIRA 16:9)
1. Institut khimicheskoy fiziki AN SSSR.
(Cyclohexadienone) (Phenol) (Nitration)
vl!

YERSHOV, V.V.; ZLOBINA,, G.A.
4-Ch:Loro-2,6-ditert-butylorthoquinonitrol. Izv. AN SSSR.
Ser. khim. no.12:2235-2236 D 163. (MIRA 17:1)
1. Institut khimicheskoy fiziki AN SSM,

URSHOV, V.V.; VOLODIKINt A.A.; BMDANOV,,G.N.
-------
Phenol-diene regroupment, in the reactions of phemols, Usp.khim.
32 no.2sl54-194 F 163. (mrRA 16:4)
1. Institut khlmlcheskoy fiziki AN SSSR.
(Phenols) (Cyclobezadienone)

YERSHOVI V.V.; ZLOBINA, r,.A.;.NIXIFOROV., G,A.
4
-
Nitration and nitrosation of 2.6-41alkylphenols, Izv. All SSSR
Ser.khim. no.10-.1877-1880 0 163. (141RA 170)
1. Institut khimicheskoy fiziki AN MR.

NIKIFOROV, G.A.; YERSHOV, V.V.
Dakin reaction in the 4-hyd*roxy-3,5-dialkylbenzaldehyde series.
Izv.AN SSSR. Ser.khim. no.l.-176-179 Ja 164. (MIRA l7s4)
1. institut khimicheskoy fiziki, AN SSSR.
Tj

NIKIFOROV, G.A.; YERSHOVxY!11,-----
phenol-dienone cozwersions during the formation of 4-hYdrcxy-3,1
5-dialkylbenzaldehyde salts. Izv,AN SSSR.Ser.kbim. no*2:293-300
F 164a (MIRA 17:3)
1. Institut khimicheskoy fiziki AN SSSR.
-h

ZLOBINA., G.A.;_Ig~,RSHOV ~V.V.~
Action of nitric acid on 4,-brom*-2p6-dialkylph9n*ls. lzv.Mf SSSR.
Ser,khim. no.2071-373 F 164. - (MIRA 1713)
1. Institut khimicheskoy fizik:l AN SSSR.
- - ;:11 "f,:!:- -
I :: --~ . 'T.~,- ;'.
I ~.. , -P i ~ - ~.:

BEIDSTOTSKAYA, 1. so; YEMHOVI V. V.
Synthesis qf 4~..~Aaftoalkyl-2,&-di-tert-butylphenolB,, Iz-v AN
SWR Ser'Mdm'JW,4;765-?6'i Ap 164. (MIRA 1?: 5)
4.0 Institut 104#oheokoy fiziki AN S58R.

BYSTROV, V.F.; YMSHOV, V.V.,I_IEZINA, V.P.
Chemical shift of the bydroxyl signal of ortho-alkyloubstituted
phenols. Opt. i spektr. 17 no.4:538-544 0 164. (MIRA 17:12)

111-P qF.Fq11qrA lit 0
UL 1 1. i 11 1
A L__ I -
H ILI
T t I
I TEP
Hli ;l: f Of I will; I ii

YMHOV, V. V. ; ZLOBINA, G. A.
-: -
Electrophi.lic reaction of nitrous acid with 2,46-trisubstit-ated
phenols. Izv. AN SSSR Ser. khim. no.11:2082-2084 N 164
(MIRA 18:1)
1. Institut khimicheskoy fiziki. All SSSR.

11
YMHOV, V.T.; ZLOBINA, G.A.
-, 1,6- -
r*
Radioal interaction between alkyl nitrites and 2,4pt(r-trioub-
stituted phenols. Izv. AN SSSR Ser. khiia. no.12a2n'., 5-2237 D 164
(MIRA 18 el)
1. Institut khimicheskoy fiziki AN SSSR.

um, B&ItE: Et
hydz--xYP?
be
AN
e~,zjjeskoy
kh'
'V, . N . K an d r ay e v y m

ZLOBINA, G.A.;
Effect of tht nature 0: substituents in 2,4,6-trAlsubstitut-ed pllenoIB
on the reaction witti nitric acid. Izv.AN SSSMrzar.k-him. no.9:1666-1675
S 164. (MRA 17:10)
2. Institut khImichoskov flziki AN SSSR.

YFR-EIfi()Vy V.V.; VOIG--T)IYIN, A.A.
--r", 1-1,
........
Si3antaneous rearrangem-3rt of orthoquinobrotaic compainds. iz,,r.
AN SSSR Ser. khLm. no.2:336-3142 165.
(IA,TRA 18:2)
1. Institut khimicheskoy flzik-; -All SSSR.

YERSHOV., V.V.; BELOSTOTSKAYA, I.S.
.4.
Synthesis of hydroxyphenylacetic acids of 'he oeries of hLnAered
phenols. Izv. All SSSP Ser. khim. no.2:376-378 165.
. 18;2)
.1. Tn5tittit kWmIchookoy flzlki AN SSSR.

NIKIFOROV,, G.A.; YERSHOVp V.V.
." - 1 1.
Radical deamination of 4-amino-2.6-dialkylphenola, 127. fill SSM,
Ser. khim. no.6:1097-1100 165.
(1,1111A 18:6)
1. Institut khimicheskoy fiziki MI SSSR.

YERSHOVY V.V.; ZLOBINA, G.A.
--l --- .- ~
Oxidation of 4-i"thyl-2,6,-di-tert-bieylphenoI by pDr.-Atercus A~---Jd,
izv. A41 SSSR. Sar. khim. no.7sl269-1271 165. (MMA 18..7)
1. Institut khimicheskoy fizlki AN SSSR.

)MRSHOV,,,-~.V.; BELOSTOTSKAYA, I.S.
Di-tert-butylspirce,yel od len one B. jzv. AN S-SSR. Ser. khim. no.7:1301-
1303 165. (MIRA 18t7)
1. Institut khimicheskoy fiziki AN SSSR.
hid, 111111il 1 1-111"

Ylillsilov 9 V . .V.; ZLOBINAy G.A. f v/.
)~, .( ". i I , ~~ ~ ~, 4
I . I i ti, r,,:- r-m! '-, r,' I.,
Roaallon of " ` I - 01,*X*PA j.,,i ))
AN S,(;SR- Ser. khlm. 165o
1. Institut khimichesk,,y fizlk~- AN SSSR.

0,
,10
SOO C, Ce 6,et
Sqeoo!:~ - e
5to-" 0i Sol
0
a's to tgbb
Jo 7p
401
C,0%09 q.%Ao
:Vw10.1 OYS
e 0t es ekes
oy
es 0 -~Ss 0
'ase ce5s
he j4 eT e C*I. 'atz.,
Cal &I ,
610 OV
t
0'
'000
W 'hevo I '00S
"o DCt* 0 00 v a
C.- t Olb ,P09 re e Cool
to . \-).c . too 10
01.6 vat . to I
tile ~,he &~ -f e -D'o ix,
ttle
Oes" - 4e i. t -
SI'm o. 'V01:
0, 0) E~ aia Al 'es
a ot t
S av
J"e
St, 95 0 Oe b Cie,%
e I , OIC
0-f S. ate c-ilf,
6.f e
.0
t :e%'3`%b-je to i0te e
th YI, 0 est
-V'- &C 0- 1
eN X1 SfJjG oss. to'?'~ "Ols e
C.OTv'? O.V? i~he a
We I j b'3- - t'? st
tlae )Y-*i ,~es
vco~- 0 O:vLes J'a Ot e.
~-Oc~ 41co
e~IA elcL
TO . OiN
'k kls ','05A!C' ez-2,. ot all, tot
'09. Be
t ea6l oce tot - 2.
10 9
-0 e
b-f
O-ts v,42,
tO
,aelv t ola
to
WNS
""0
~,'o 5 '119 oiv.
B
v s '? ea's
0y
00
t'CO oce 'j-0 OY-W
? );~e t
~ts

L 369731-66
ACC NR: AP6008511
SUB CODE: 07/ SUBM DATE: ZOMay65/ ORIG REF: 010/ OTH REF: OOZ
c
z

VOLODIKIN) A.A.; OSTAPETS-SVESHNIKOVA, G.D.; YERSHOV, V.7.
Reaction of organomagnesito compounds vith
4-hydroxy-3,5-di-tert-butylbenzyl bromide. Izv.AJ[ SSSR.
Ser.khim. no.3.2:2188-2190 165. (MIRA 18:12)
1. Institut khimicheskoy fiziki AN SSSR. Submitted April
2j 1965*

for
cv.
C o
1 7 7
hi
1",av

:1 1, k~,'..rrd rhf- skcy 1'i L; ki AN

LEMEDEV, A.P., doktor gecl,-mina, otvo red*; YIRSFOV, IL-V -~ red.
[Characteristics of the fo-rrAtion of basic rocks ar-d ~of
the mineralization connected with them] Osobennost.i. for-
mirovanlia bazitov I. sviazannoi s nimi minoralizatsti.
Moskva, Naukap 1965. 226 po (14TRA 18:31)
1. Akademiya nauk SS,11. Institut geologii rudnykh rnoiito-
rozhdeniy, petrografii, mineralogli 1, geokhimill,

AL

LiLifldl I 11-IL -1-- 1 -7... j L"Ll,
it I I
LU 477
CIA, kAl
:1 ii I IT! NM,

YERSHOVP T.V,
Equations for sandwich plates of variable thickness. 1zV.
Vys, ucheb, zavo; &v, tekh. 7 noOrl9-28 064. (MIRA 17s9)

History of the Yaro-lavl Rubber and Asbestos Combine. rauch. i
rez. 16 no.11:34-35 N 157. (MIRA 11:2)
(Yaroslavl--Rubber industry)
(Taroulavl-Asbastoo)

LILL ~l Ij
Ildill"

YEILSHOV, V. Z.: 11.1aster Geolog-Minaralog Sci (diss) -- "Laws of tha
tion of coal-bearing strata, on the examples of the Donets and Llvov-Voljnf
black-coal basins". L'Vov, 1959. t6 pp (Min Higher ~,(Iuc ukr 8SR, LIvov SL;Its~
U im Iv. Franko), 150 copies (KL, No 13, 1959, 101)
. ; I I --- 11 -! . I 11 .; ";F-
1~; !,'f, ~ -, lj~- .. - .
1.. -4,5'- !: A,

YERSHOV, V.Z. [IErshov, V.Z.1
Some characteristics of the origin and development of the voleanic
formation in the Lvov-Volyn Bacin. Pntoi Irot. gool. kor. kcE).
All URSR 2s69-82 160. (MIRA .14:5)
(Lvov-Volyn Basin-Coal geology)