SCIENTIFIC ABSTRACT GRAFOVA, Z.M. - GRAIF, A.L.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000516520006-6
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: March 13, 2001
• Sequence Number: 6
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

GRAFOVA., Z.M.
@- , " &@-
Deter-mining nickel as ammoniate. Khim. i khim. tekh. I-
219-224 162. - I .
Reaction of nickel and dimethylglyoxime interaction. Ibid.:225-228
(MIRA 17:2)

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t - - -.Z 1 1- @ - :i --

ZHHMOI A.Tj--QBAFMykt-2@.S.; CHERNIKOVAJ N.V.
Produaing "pure" vitamin D deficieney in rats. Vopipit 21 no,4s
71-74 Jl-Ag-162. KRA 15:12)
1. Ix..Nauchno-isoledovatellskogo instituta vitaminologii
Miniaterstva, zdravookhranoniya SSSR, Moskva.
(DEFICIENCY DISEASES) (VITAMINS-D)

iggi
t4
TV
ask
ER

YUDIN, Ye.Ya.;. CIL -I.A.
Investigating the design of anechoic chambers. Prom.
aerodin. no.l4zlO9-127 '59- (MIU 13:6)
(Acoustical engineering)

. - - - -1 ......-
-GRMKIYj I. kva)
Instruments for the meamwement of noise. GigA oan. 25 no.9:50-53
S 160, (NOISE-MMUMENT) (KMA 3.3:9)

LYCHKINV V.M.; GRAFSKIY, N.I.; POKOYEVA, P.S.; RAVIN, V.M.
Proposals of .the efficiency promoters of the Saratov oils and
Fats Combine., MEtal.-zhir. prom. 29 no.800 Ag 163.
(KIRA 16: 10)

GRAFTER, Te.L.
. Improved synthesis of di- @j@ -chlorce0ql enter of (S-chloro-
othylphosphinto siaid. ;hur. ob. khim. 28 no-7:iqo8-lqdq n 158.
(MIRA 11:9)
I.Nauchno-iseledovatellskiy institut plasticheskikh was.
(Ethyl phosphites)

MAVLYANOV9 G.A., akademik, oty. red.; KENMARIN, N.A., sam. otT.
red.; KRYIDV, M.M., prof., sam. otv. red-; jOjR4nRqV,
V.G., kand. geol.-MIni nauk, red.; KHASANOV, A.S., kand.
nauk, reC; KHODZHIPAUV, N.N., kand. geol.-
min.nauk, red.; IVANOVA, M.F., kand. geol.-miner. nauk,
red.; ISLAMOV, A.I., kand. geol.-min; nauk, red.;
SULTAN-KHODZHAYEV, A.N., red.; ASTAKHOV, A.N., red.;
GORIKOVAYA, Z.P., tekhn. zed.
(Conditions in Uzbekis@4n from the point of view of hydro-
geology and engineering geology] Gidrogeologicheskie i in-
shenerno-geologicheakie usloviia Usbakistana. Tashkent,,
Vol.l. 1963. 194 p. (M RA 16: 8)
1. Akademiya. nauk Uzbekskoy SSR. Tashkent. Institut gidro-
geologli i inzhenernoy- gwl*gU. 2. AN Uzb. SSR (for Maylyanov)
3. Chlen-korrespondent AN Uzb.SSR (for Kenesarin).
(Uzbekistan--Water, Underground)
(Usbokistan--Engineering geology)

B.
CHERNYSI]EV) V. V.; ERS.H=o
BYAKOV, V- V@; GRAFLITIN, V-
boiling liquid."
Nest transfer in a
anef6r, Kjsk, 4-12 W
report submitted for 2nd All-Union COnf on Beat & Tr
1964.
:rnat 'PeriMental pllysiCB.
f TheoretiCal & Ey
0

GRAFUTIN, V. I. ;_ SUBBOTIN, V. I.; SUVOROV, L. Ya.
"Heat transfer in liquid-metal-cooled reactor elements."
-report submitted for 3rd Intl Conf, Peaceful Uses of Atomic Energy, Geneva,
31 Aug-9 Sep 64.

BYAKOV) V. M.; GRAFUTIN) V. N.; SUVOROV, L. Ya.
"Dynamics of boiling steam-and-water mixture.H
report submitted for 3rd Intl Conf, Peaceful Uses of Atomic Energy, Geneva,
31 Ai@-q Sep 64.

JillI

0 rZ
95

FALASHIVSKIY, A.M.; SYPCM, P.P.;
High-speed recording device. Vop. rasch. I konstr. elektron. vych.
mash. no.1:123-i3l 160. (MIRA 14:1)
(Electronic calculating machinee-Input-output equipment)

GRAGEROV, I. P.
USSR/Chemistry - Phanols Aug 1947
Chemistry - Hydrogen
"Hydrogen Regrouping, in Phenols," A. I. Brodskiy, Corr Mem, Acad Sci USSR; 0. P. Miklukhtn;
I. I. Kukhtenka, I. P. Gragerov, Inst Ph)s Chem imeni L. V. Pisarzhevskiy, Acad Sci USSR,
3 pp
I'Dok Akad Nalk SSSR, Nova Ser" Vol LVII, No
Ird icates that certain reactions in aromatic compounds may be expressed as follows:
and studies the special case wnere x 0 and y = H.
PA 5M

GRAGMOV, 1 - P -
Iu. K. Inrtev, M. G. Voronkov, I. P. Gr@.Ce_rov and G. Ia. Kondratleva, The re@,cfion
of/ -bromo-fumnidine with the Grigmrd Roagents. 1. @_ 18,-)/,
The tetra-hyiro-furane-halides in which a halogen atom is in a /J@Po2iti-3n
Uo an oxygen atom, reacts with the GriEnard reagent to form very sluggishl-, mixed
magnesium-organic cormouns which for the most part rearrange with t--e 0-.ening
of the cycle into magnesium-halide-alcohol' 'Les of 'r -unsaturr-ted pzlirnary alcolnols
and react in a part on ti-e normal type as Grigard, reagent.
The Lomanosov 3tate University in Moscovi, Holder of the Lenin Ctcier
The Zelinskii La'. of Organic Chem., September 22, 1947
SO: journal of Gereral Chemistry (USSR) 38, (80) No'. 10 (1948):

GRAGMOV, I. P.
Iu. K. Iurlev and I. P. Gragerov, Synthesis of /alkyl-furanioines. II. P. 1811
This work gives a general method for the synthesis of /4-alkyl-furanidines by
interaction of lithium alkyls with Igbromo-furanidine. It is shown that the re-
action of lithium on/9-bromo-furanidine causes the opening of the ring of the
latter to occur with the formation of allyl carbinol.
The Lomonosov, Moscow State University, Holder of the Order of Lenin
The Zelinskii Lab. of Organic Chem., SeDtember 22, 1947
SO: Journal of General Chemistry (USSR) LB (80) No. 10 (1948):

OWEROV, 1. P.
25401. GIRAGEROV, ll.@Pl V. 11".
Spel-try kcxnbinatsionnogo rasseyaniya t-lofana i e.go goxiojo@gov. Zhurnal fiz.
Khimii, 15048, VYP. 7. 783-86. Bibliogr: 6 Nazv. Sm Takzhe No. 25427
0
SO: Istopis' Zhurnal Statey, No. 30, Moscow, 1948

USISR/Cheristry Synthesis Furans Oct 48
"Synthesis of BeLa-ldkylfuranidines, II," Ir. R. Yurlyev, P. Grac-erov,-
A L;
Posco,d Ord of Lenin State U imeni. 11. V. Lov@,nosov, Lab of OrC Chem ireni
Acad N. D. Zelinskiv, 5 pp
I'Zhur Otshch 1@1,jrll Voi XVIIIJ. 140 10
Gives general. method for synthesis of betrL-alk~rltetr.,iiydrofurans 1,,, reacti,-.)n
alb-yls with beta-bronictetrahydrofur6. Hin" open3nL- occurred
of lilbiull
by action of Mg :,n beta-bromotetrahydro-furan with forr.-at-ion of 3-buten-l-ol.
Submitted 22 Sep 47.
PA 2/5OT68

-CA
is ij;j 04
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so
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Colo# or aft;
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00 k the D Rs LaA S S
cah(ou)% WkI by almost bftt- zoo
00 qwWwwooddil DK*M?% QW1110019 kh
00 at too Mier 10-4 006 us looked in
'Ref tin D, WKS 0% imod.0
7, goo
00 "dw tbw iisomm". CWW
goo WAIN dowill goo.
41 j*% the imp. moo
tlz DVON On p
god wor
gow didwab-Alp""Agow -a bro. fovi
140 aw
a tbw sm. ma do do. D va 6 too quismor.,
IW
41 do so tin VAUM ww-
tons, ar wed. th
&wIffA�.lb=wtI0 goo
0 (44.). Ilm w-
40 @rw
%
2 1 OW, u%btb= to the qw=.., 0
tw dDIIIIIIIIIIII M4W FA 70% cm Y
10 AtImi" 040. 1 --
ago at mwj;w CJ)A
be 4m so bwkme a goo
+ + thb uumitim
It atom b too =4 -
oppmd by a 140 MW ;1;;Wr.
620dom ~== (Owed - Pro, too
&To% a TWO-
44TALLURGIC&L wow,
SIA4114144 A I I I "d 6 9 A 4
Sam S too 4mv 99
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2blopbenep T*tr8hY&O--ASW 49
Fpr@up Totrallydro-
:*2M C=verslon of Alpha-Beta- and AlIqlAiranidinse
Mato Moir Corresponding 22ilophanes., 33;LU."
Ift. X. 7=27ev,, 1. P. Gragerov, Moscov Or4 of
@" State U Imeni M. V. Lamonosovp Lab or Org
am 1meni AcaA N. D. Ze3lnski7;, * Yp
'!Zbzr Obahch Shle Vol =1 NO 4
Alplha-allql- and beta-alkyl-thiophmwo are pre-
pared. by the subject reaction., vhIch gives a
S"ater yield (72-81% of the-theoretical) of the
beta-allql-thiophames than 8f the alpha-ccmpomde
65/49MB
#M/Cbemistry Thiophene.,. Tetrahydro- Apr 49
(Contd)
@(*bwm yield is 65-70 of the theoretical).' So
tomw also have higber boiling points,. B"Oifie
ipmvIties, and, Indexea of refraction tium the:,.''
latter. Ehftl 31 Jan 48.

6,-f
TraNdWINDO&M Of - And $4111111YVINIUMMI114,11 Will IM
cervespesilft a. and 41-alkylpynallidis". ZXV1. Vu.
K 'Vur'ev and 1. P. Gram (Lotoonomov State Vniv..
Kow"). ZAmr. ObAlw Khow. J). Own. Chem.) 20,
171-4(IOM)): of. C.A. 44. 14W.I. 44114th.-Alkyllmralli-,
y4frofilrall-A) %tvir 4-tollywiled to the rtw.
kylpyfrull,lillett If) by druppills theill 01-7
"trong Nits oitreant jacco an AltOo-fillott
Illive- at 31,W; frvih vat;jIv,t w.&% tvw,I (tit rach run. The
1#41,1willif I air firwrillrd, .1-Ale IMP', InIm J-Wlkyl-
j.p.saidlao,). I"I I(rj .11% 1-1 0.8kh). *If 1.44JOI It-110.
jjl@ 1141.11) 1.6"), J.P.1 11111; 1, b", 1:11'. Ill- 10 Mill, "I,*
I. MOI (pitrak, Ill. lol - J-pr In.4 158'. dl,
[e-mail]
Rill
4

The -br*"M bwd is. ow do ooom St.
W.. 1--himmmal G. P. miklukhin
rm. Is., Aw. ft. KUM. 24.
AM409W). d. C.A. 4A. 4&28,@-H -,ulm- (t) and
tb* isdi qminbydwm:
"WWI; i
quimm (M
) W
w SMoltim (w n@) R brtwmn tbc:'
wbo dw . abubm wm I "d c4DA (111)
4w hem U wd w(CON), (IT) im BW wwA mMiowd. the
WbNWAtO WW = (at W%) I ilk im fim OW IV'
in ibe 3ad knimm. ( imp. cd mhkmtkm was
varied ft@ 70 to 107*.) Wbm -
,,nd IT we. pptd- ,h ...COH,.r, itt'nakof -ifthle,
quhmw obtak" eMaind 21@@ M drpmd6g - the
AV. Kidily ad MW. qj tk Sda, IV wo p"d. by
hming I Ah DoO iwd NOOK at 170* OW ti-Ift tbr
pFudwt okk IW; k m. 173*. M wm pmpd. frm IV
+ NaQ ad m. 1130. PftwmmW OW in Otb- in-
rH bmW, H bW a Pch IW Wim.
J. J. 4.

ASSR/Chesistry - Isotopes Oct 51
"Heavy Water," 1. P. Gragerov, Cand Chem Sci
"Nauka I Zhizn"' Vol XVIII., No,10, pp 12-14
A. I. Brodakiy, Corr Mem, Acad Sci USSR, and his
group were the lot to obtain heavy water and
heavy water concentrates in the USSR. They de-
veloped a method for the sep detn of deuterium
water and heavy oxygen water in natural waters
by measuring sp wts and indexes of refraction
in pure samples. Geochemist A. P. Vinogradov,
Corr Mem, Acad Sci USSR, et al did interesting
vorIr on the origin of minerals by investigat-IrS the
213T24
IsotopE compn cr water prepd from the oxygen con-
tained in the minerals. Heavy water and
deuteroparaffin are the most effective moderators
in atomic energy piles.
C-D

jiftw of 6=0 POMMMI barrier in as 106cof
dl*
A. 1. Wdsion .@'
1.
Onwerov
ItM- Ploys, C111013. Aced &4-.VkW-
S-S It- Met) Dakinify AW. Aak, @.S.S.R`. ". 277-
fate Of "wributiou of D between quinow
Ond bydfOquinme Ott ning In the decompil. the
qmWb,rdrone, CD40IIh-C#IIQ,, was ed at I
I ISIX), anol 119 A , Jibe rate 6 Ism, top to 0 t
X - 0.1 (z - fraction of 13 pas"'i h
WMIrl to
lluinom- at Mud. it Is atioutned that x. . 0.5). The "
r-CliM r-Poltuble for the deviation from the Idordcr
kkwfkz at Wer -11axes Is no clear, that it is not osoidatkon
fallenst loreen the fact that vieptacement of sk by N, don
so th"" a- In the Ist-ader range, 10% - ON. S.W.
" 7.08 sec.-J, resp., at The 3 tcorops. This gives log k -
2COM - (11.10 X ioa/n. hence the actitation twu
R - 50.314 cal./mok. This 6 low" than the true value of
A wbich should be ceded. to@h - AI(EaRLZ@0-11(4
I)IIA-010t. whom as - no. the vibrat degrees d
freedom entering Into dw activation enemy. TDA $IV"
for the UM activatim coma E - M4 + R?Xn - t),
On the am tion that the inimial viLwaiWas am lowely-
bound witIsIntg: werval vibratloon, quinhyd.ooe may be
considered " a system of 8 owiltating centers whiA c - 18.
We gives A - 63.3W cal./mole. and A - 3.2 X 10's
we.-' The value 8 - 03 kcal./inde is e"ImInIT elm to
the upper limit. It being very probable that the P~
of the 2 hydroogenbooded H atoms in quishydrone takes
piece simultaneously (which Is bome out by the - ofa
kuimooocs). the height of ma potential
buriw..7g. the 2 min.-coemy equil. positions OU ... 0.
and 0. 0 Is R/2 - 32 local. /mole from the sem vibra-
tioasl level or 37 kcal./awk from the bottoin of the paten-
tial wall. This high value is 111dusible in view of the derp
MM" bon4le Involvoil In the transition C#D.-
10100= 01 C.11A.C.114011h. The Its valvat of
Aisexplaiwdbyactivai6mthfuu#btmmfw vibrational
energy in the crystal lattice. as contrasted with the trans.
fer of trauslatimal khwtk energy in collisions beta pose.
ousmob. Possibly the reaction proceeds by stchain mwba-.
06M In the lattice. 14. Then

GRAGRWV,,I.P.; BRODSKIT, A.I.
Mcparimental determination of the degree of the potential barrier in
hydrogen bonds of benzoquinhydrone. Zhur..ob.khim. 23 no.7:1193-1199
J1 153- (MLVA 6:7)
l..Institut finichaskoy khimii Iment L.V.Pioarzhevskogo Akademii nauk
Ukrainukoy SSR. Mrdrogen) Npiubydrones) (Blectromotive force)

ussn/ Chemistz7 Analysis methods
Card 1/1 Pab. 151 9/33
Authors Graferov, I. ps
Title Exchange of radicals between orgWz compounds in a solution
Periodical Zhur, ob, khim. 24/8) 1321 1326, August 1954
Abstract The exchange of mtb;yl, etbyl and pherorl radicals between a number of
organic compounds in a heated solution., was investigated by the isotope
(marked isotope) method. The data obtained are explained on the basis
of representations.concerning the exchange of radicals with intermediate
forim;,tion of onium compounds, A parallelism between the easiness of
of interchange reactions and all7lation reactions., was established.
Elevon referencesi 2 USSRo 3 USA, 4 German and 2 French (1867 - 1951).
Table.
Institution s Acad, of Sc. Ukr-SSR, The L. V. Pisarzhevskiy Institute of Physical
Chemistry
Submitted Febroary 15, 1954
77

0
,Chemistry - Exafianke reactions
card 1/1 Pub. 151 - 11/42
Authon j,'Grdgerov.! L., P.
title Uchange of bouhd radicals into free radiccilb and ions in solution
Perlodlaa ',ihur. ob.,khim. 24/9., 1542-1547.. Sep 1954
Abstrast !the possibility and conditions leMing.to exchange reaction of D2 mark-
od, free phenyl,- methyl mid etVql radicals and phenyl positive ionq and.
i-,he very same radi6als.included in the composition of canpounds were
3.nvestigated. The isotopic.investigation method made it possible to
observe the exchange of identical radicals, to study the laws governing
the exchange and to distinguish the reaction products. Exchange reac-
tions were observed only in the case of the free metbyl and ethyl radi-
cals of photochemical origin. Ten referenceez 7-USSR; 2-USA and 1-
German (1888-1954). Table.
Institution A.cadenV of. Sciences Ukr-SSRJ, The L. V. Pisarzhevskiy,Institute of,
Phys.-Chem.
Submitted February 19,,1954

'E" R
oi
SM
i 1 -01, Oil I I I
-rT

lissn/Chemistry Phyalcal chemistry
'Card 1/1 Pub 151 - 112/37
Authors ...t Gragerar, I. F6
Title' Mobility of hydFogen.atoms in hydrogen bonds of phenazhydrine
Pdriodical Zhur, obo khima, 24/19, 1769-17710 Oct 1954
Abstrac@ The obtained
mobility,of hydrogen atoms, in hydrogen bonds of phenazhydAw,,,'
'from heavy-phehatine and.ordinary dihydrophenazine, was investigated, Split-
ting of.phenazhydrine into components yields phenazine and dihydrophenazine
containl=
equal amounts of deuterium This phenomenon is exp13,ined.by the
origination in the solution (durin@ the preparation of phenazhydAne) of an
oxidation-reduction equilibrium between the negative double charged-dihydro--
phenazinB ion and phenazine The structure of phena:zhydrine with. localized
hydro en in the hydrogen bonds is descrited. Two references': 14SA and 1-
USSR F19.34-1953).
.Institution t Academy of Sciences Ukr-SSR, Institute of Physical Chemistry
Submitted February 15, 1954

Ji
V@s g IWdy of irstdiw in
birly by the 1"to a method
AD
P. Gr'agmvi
Daklady U . 1N'4Uk S.S.Tft, 99, Ibf!T'
cortinututicatiuns weit found in the litera-
tute on the dotible demulm, ft-actiolls of ulkyl and dryl
ihOlleab that give direct infomiation on the pro1wrties and
'n'ct imedwi-syn 4 org. substances. Reactions be-
tweett free railicab and carbonium ions are also of intemst,
5. they are --ned to p-
C re" 4 or .th the
=Itdol'y ati
d sornewliat 1,
radicatsi. In the present investigation the 2 reaction types
were studied by ingjiu.- one of the reaction particip-ants with
-,s foutidnot to interait with phenctole,
Datoms.. C2D&Brw.
!or with MOAc. @CJIJ does. not interact with ani.@ole'
@wherr'e; (Cj)j)jSOA !at acts readify with AM and with
'AWAc, but not with fie niethyl ether uf p-toluciimulfouic
acid. The difference 16 behavior 6 explained oil tile ae-
mptor-donor theory, and tile dOUIAC CXCIM11gi! Of the radicals
EkTreases in the ordalli:1504 -# Et2F,04 - phenctole. No
doubit! exchange mactions were observed with tile Pit, Me,
--aid I
A riulicAi, tir with the pos. pheny] ions, the phenyl
milicals being obtuined by th(anal dminjul, of the heavy
pheny1diazonium chla6le, or the ph6tochein. decompm. of
the heavy iodubtuiene. CD, and C,D. radimL. obtained:
photoehemic;tIly, tin interact with anisole, phenetole, Me Bu
ether i
and Qt',t).U, but slowly, in conintiliction of results,
obtuisi4!dbyK]iar.L-,Is,etal.(C.,1.37,307il). Th@,mcthuljl.
of production of Ileavy-hydrogol t)Tg. compti". ii de,5.-@bcd"
W. M. St"11Wrg
mal.,
VQrr-@A! ='.i-; Q.,
g.M.M. W,

V Exchartga reactions of free end bound radicals Iii solution.
I. P. * Grage
-rov Vaprosy Khios. Kincliki, K=M V i
Oixalfil AV-
him. Nauk loss, 30-O.-Istur t 64UII ;S74Wt-IoCOS'IrkO'E-
tr
r
exchange Rt radicals even at 1950 with EtOPh cc EtGhc.
similarly, LibcIed Pit I does not exchange radicali with NUO-
Ph. Appreciable exchange (25%). occurs between labeled
and unlabeled EtI, but not between Etl and EtOPh or
bet'.'ceu- Mel and McOPh. Exchange between EtBr and
EtfsOa occurs ireaAily -at 15.1)*. D-labeled MerSO, ex-'
changes Me readily with Wel or McOAc itt 125-55', but
not with P-?,leClf4SOjINfe, but the latter "changes rcadily,
withMclatI55*, In the presence of AcOll, EtBr exchanges -
Et 'Aith IROAC at 1950 . but AlBr. does not cause (at 60*)
an -exchange between EtOPh and EtDr. The resnits are,
attributable to intermediate formation of onium compds..
A parallelism exists betm\-a the ease of radical exchange
and alkylating ability. With Pit radicals either from ther-
mal deconipit. of D-labcIttl PhNjCl or photo-chent. cleavage
Of labeled Phl no "change was detected in solas. of MO.
Bloph, 111111C. or Pill; similar lack of exchange with these
solvents was found "ith Ph+ ions from decouiptt. of PhNv.
B PI., . D-labeled Me or Rt radicals from photodecompn. of
the iodides exchange moderately readily with 'MeOPh,
FtOPh. Afe0fle,and.rit. However, Me or Et radicals
.0.
formed from reaction with EtMgBr do not exhibit such ex-
change. The results contradict those of Kharasch. el at.
(C.A.-37, 30787) and Shaw (C.A. 45, W42c).
G. M. KosoLALOI.

Abstract I Experttents-ware conducted for the purpose of obtaining more-positive
data@on
the isotopic oxygen exchange in various bydroxybenzenes and
nitrophenols as well as in acid and alka4,media. The exchange process
was investigated after reduction of the 0-11u content in the heavy-oxygen
water then enriched 4-5 tinies with the very same isotope and freed of
any excess deuterium. The entire work was carried out by mans of a
conventional flotation method and the resmlts obtained are described.
Four references: 2USSR and 2 English (1938 and 1952). Table.,
Institution Acid. of Be-- Ukr-SSR. The L. V- Fisarzhevakiv- Inst- of Phvn- Chpm-

GRAGEROV, I. P.
"Rapid Mass S-pectrometric Method for the Isotopic Analysis of Oxygen in Organic
Substances."
W-To
p.,objeW Zj=tIc-a end C--t-,Jr-i8y V- 9, 150tO
= SSOR, 1957, 44-11p.
Ltw& CT tho purrs In th,10 ec@uertioa V,-re Prom-mubi at the Cmr. COD
to
uotcrzza tn C%ta3zmin ifmieb tc;@ rln=, im Mcn-1vu., ',*= 31- ArT 5P 1956.

SOV/20-121-2-28/53
AUTHORS: Lbramovich, T. I., Gragerov, I. P., Perekalin, V. V.
TITLE: The Isotopic Exchange of Hydrogen and the Capability of the
Methyl Derivatives of Nitrogen Containing Heterocycles to
Enter Into Condensation Reactions (Izotopnyy obmen vodoroda
i sposabnostlimetilinykh proizvodnykh azotsoderzhashchikh
geterotsiklov k reaktsiyam kondensatsii)
PERIODICAL: loklady Akademii nauk SSSR, 19589 Vol. 121, Hr 2, pp. 295
298 (USSR)
ABSTRACT: The heterocycles mentioned in the title which have a methyl
'radical in an cc- or r-position to the hetero atom, as well as
their quaternary salts enter into condensation reactions with
aldehydes, nitroso-oompounde, diazo-compounds, nitroolefines
(Ref 1) and others. These conversions usually take place in
a.a alkaline medium. These compounds can be arranged into a
series as regards their activity . The opinion (G.gG as
mentioned in Ref 2) that the velocity of the condensation
reactions as well as the possibility of their course at all
Card 1/4 is determined by the easy cleaving-off of protons from the

SOV/20-121-2-28/53
The-isotopic Exchange of Hydrogen and the Capability of the Methyl DeriTati7es
of Nitrogen Containing Heterocycles to Enter Into Condensation Reactions
meithyl radicals, is widely spread. As the said easiness is
quantitatively characterized by the velocity of the isotopic
exchange of hydrogen in an alkaline medium it was interesting
to compare the velocity of the exchange of the compounds
mentioned with their tendency to condensation reactions. By
doing so also the factors could be explained which determine
the mobility of the hydrogen in the methyl group in dependence
on its structure. In the present paper the authors investig
@ated
the exchange of hydrogen between the compounds of the series
(1) and the methylalcohols CH30D in the presence of triethyl-
amine. The ratio betweqn the substance investigated, the
alcohol, and the catalyst was about constant and amounted to
0,007 : 0,03 : 0,001 moles correspondingly. Figure I presents
the results obtained as the function of in (i - z) versus the
duration t, where z denotes the share in the exchange calculated
in relation to the three hydrogen atoms of the methyl radical
subjected to the exchange. The points obtained in the experiment
may satisfactorily be located on the straight line describing
Card 2/4 the time course of the reactions of first order. The mean

SOV/20-1121-2-26/53
The Isotopic Exchange of Hydrogen and the Capability of the Methyl 'Derivatives
of Nitrogen Containing Heterocycles to Enter,Into Condensation Reactions
values of the velocity constants K (Table 1) were found from
the slope of this straight. The exchange of the above mentioned
expe-rimenta.conoerne only the hydrogen of the methyl residues
be:Lng.inEn a- or j1hposition to the hetero atom (the hydrogen
of the N-Hbindings.is not included). The consecutive order
of the exchange velocities reflects the differently easy
cleaving-off of protons from the methyl radicals. The comparison
between the series (1) and the data in table 1 shows that the
activity in the condensation reactions does not correspond to
the tendency to the cleaving-off of protons. Thus the ionization
of hydrogen, at least in several cases, does not represent the
limiting stage of condensation reactions.
,rhere are 1 figure, 1 table, and 11 references, 8 of which are
Soviet.
ASSOCIATION: Leningradskiy pedagogicheskiy institut im. A. I. Gertsena
(Leningrad Pedagogical Institute imeni A. 1. Gertsen)
Institut fizicheskoy khimii im. L. V. Pisarzhevskogo Akademii
Card 3/4 nauk USSR (Institute of Physical Chemistry imeni L. V.

SOV/20-121-2-28/53
The Isotopic Rxchange of Hydrogen and the Capability of the Methyl Deriyatives
of Nitrogen Containing Heterocycles to Enter Into Condensation Reactions
I?isarz.hevskiy7AS UkrSSR)
PRESENTED: Harch 18, 1958j, by A. N. Frumkin, Member, Academy of Soienc*st
USSR
SUBMITTED: Harch 17, 1958
Card 4/4

/001/904/067
BI56/B101
AUTHORS: Brodskiy, A ii, Grageroy -?-, Franchuk, I. F.p Sulima, L*V.,
Kukhtenko, . Ama:--@ A., Fomenkoq A. S.,
Aleksankinp M. Lt.
TITLE: Mechanism of oxidation reactions investigated by the isotopic
method
PERIODICAL: Referativnyy zhurnal. Xhimiya, no. 1, 1962, 60, abstract
1B439 (Tr. Tashkentsk. konferentsii po mirn. ispollzovaniyu
z.zomn. energii, v. 2. Tashkent, AN UzSSR, 1960, 327-334)
TEXT: A reviea of work done by the authors on studying the mechanism of
certain oxidation reactions using isotopes: the oxidation of organic
compounds with chromyl chloride, the mechanism of anthranil regrouping, the
process of oxidation of aniline, o-anisidine and p-nitroaniline with Caro
acid. The mechanism whereby hydrogen peroxide and certain persulfate-type
inorganic peroxide compounds are Xormed and converted is examined; so also
are the kinetics of isotopic exchange in substituted benzoic acids,
Card 1/2

S1081V621000100110041067
:.'Lechanism of oxidation reactions ... B156/B101
18
benzaldehydes, alcohols, naphthalenes and nitro compounds with H20 .
18 references. [Abstracter's note: Complete translation.]
Card 2/2

GRAGEROV, I.P.; LEVIT, A.Y.
Mochanism of the oxidation of womatic amines and nitroso
compounds by Carols acid. Zhur. ob. kbim. 30 no-11:3762--
31131 N160. (MMA 13:11)
1. Inetitut figicbeekoy kbimii Akademii nauk USSR.
(Amines) (Nitroso compounds) (Peroxymonosulfuric acid)

MIKLUKRINO Gleb Panteleymonovich [deceased]; Prinimall uchastlye:_%j__,
,I-P-, kand. khi . nauk; REWBEVA, A.F., dand. kbim. wil ; POKHO`V-
SLUA9 Z.S.j red. izd-va; RARIMINA, W*P*j tekhn* red,
(Isotopes in organic chemistry3 lzotopy v organicheskoi kbimii. Ob-
rabotka, i dopolneniia I.P.Gragerova i A.F.Rekashevoi. Kievj Izd-vo
Akad. nauk USSR, 1961. 730 p. (MMA 14-- 7)
(Chemistry, Organic) (Isotopes)
1*

GRAGEROV., I..
"Isol;ope exchange and substitution of hydrogen in orpnlc
compnindo in the li&t of the theory of acids and bases"
by A.I,Shatenshtain. - Favieved. by I.Grageraw.
Ukr.Ildm.zhuro 27 no*6-.831-432 161. (MIM 14:3-1)
@ffydrogen-lsotopes)
(Shatenshtein., A.I.)

,,"@EROV, I.P.; REKASHEVA, A.F.1 TARASENKO, A.M.; LEVIT, A.F.; SAMCHENKO, I.P.
Syntheses of certain organic compounds labeled-Vith 018.
Zhur. ob, khim. 31 no,4:13.13-3-U9@ AP 1.61. (M@ 14:4)
1. Institut fizicheskoy kbizali imeni L. Pisarzhevskogo
Ake.demii nauk Vkrainskoy SSR.
(Oxygen-Inotopes)

ABRAMOVICH, T.I.; GRAGEROV, I.P.; PEREKALIN.. V.V.
D!qtopic hydrogen excban&o in connection with the tendency toward
condensation reactions* 'Zhur,ob,khi-, 31 no*6:1962-1968 a 161.
(ML 14;6)
I* Iustitut, fizicheskoy k4im" im. L.V.Pisarabovskogo AN Ukrainskoy
SSR I Leningradakiy.podagogicheskiy *titut imeni A.I.Gertsenao
" (Condensation products (Chemistry)) (Deuterium)

ALFXSAINKIN, M..M.; GRAGEROV, I.P.
Mechanism of the oxidation of aldehydes by oxygen in an aqueous
zedi and of isotope exchange of substituted benzaldeh@des with
H201r* Zhur.ob.kbi-., 31 noolO:3167-3170 0 161. (KMk 34:10)
1. Institut fizicheskoy khi?nii imeni L.V.Pisarzhevskogo AN
Ukrainskoy SSR.
(Aldehydes) (OXYgSll--I8OtOPSI3)

GRAGEROVY I.P.; TARASENKO, I.M.
Isotopic method used in studying the hydrolysis of salts of
methylstafuric and othyloilfuric acids. Zhur.ob.khim. 3.1
no.l2s3878-3880 D 161, (MMA 15:2)
1. Institut finicheskoy khimii imeni, L.V.Pismhevskogo AN
Mcrainskoy SSR. (Methymilkwic acid)
(Ithystafuric acid)
(Hydrolysis)

GRAGEROV, I.P.; TURKTNA, M.Ya.
Isotopic and mass-spectrometric method of investigating transfor-
mationF of phenyl, radicals in solution. Dokl. AN SSSR 140 no.6:
1317-1320 0 -61. (MIRA 14:11)
1. Institut fizicheskoy kbimii im. L.V.PisarzheV5kogo AN USSR.
Predstavleno akademikom M.I.Kabachnikom.
(Radicals (Chemistry)--Spectra)
d

BRODSKIYq A.I.; GOLIDEMLID,, I.V.; GRA R.-OVP I.P.
Isotopic analysis of oxygen in vater by the persulfate method,
Zhur.anal.khim, 17 no.12893-895 0 162. (KMA 15S12)
1. Institute of Physical Chemistry, Icadev of Sciencess
Ukrainian S.S.R.
(Oxygen-Isotopes) (Water-Analysis)

BRODSKIY, A.I.; POKEOIENKO, V.D.; ALEKSANKIN, M.M.;,GRAG WV, I.P.
Formation and deco"sition of cumene hydroperoxide in H2018.
Zhur.ob.khim. 32 no.3058-760 Mr 162. (KERA 150)
1, Institut fizieheskoy khimii imeni L.V.Pisarzhevskogo AN USS.
(Hydroperoxide) (Oxygen-Isotopes)

BRODSKIY, A.I.; ALEKSANKINV M.M.; @@EROV, I.P.
Mechanism of pyruvic acid oxidation by hydrogen peroxide.
Zhur.ob.khim. 32 no.3:829-833 Mr 162. NRA 15:3)
I.. Institut fizicheakoy khimli imeni L.V.Pisarzhevskogo AN USSR.
(Pyruxic acid) (Hydrogen peroxide)

GITIS, S.S.; GRAGEROVj GLAZ, AJ.
Reactions of aromatic nitro compounds. Part 13: Isotopic method
of'st,~idying.ddditioh'products*of alcoholates to trinitroanisole.
Zhur.ob.khim. 32 no.9:2803-2805 S 162. (MIRA 15:9)
1. Institut fizicheskoy khimii Aneni D.V. Pisarzhevskogo AN
UkrSSR.
(Alcoholates) (Anisole)

GRAGEROV, I.P.; PONCMARCOK, M.P.
Kinetic isotopic effect of deuterium in the Etard reaction.
21m, objrhim. 32 no.11:3569-3575 N 162. 1 (MIRA 15: n)
1. Institut fizichaskay khimii imeni L.V. Pisarzhevskogo
AN UkrSSR. . (Deuterium compounds)
(Etard reaction)

AUGEROV, PONW"HUK, M. Pe; STREUO, V. V.; GANIUA-,, L, N.;
VYSOTSMI Z. Z.
Free radical formation in binsbouiubydrone and pbonasobydrin
on solid surfaces 'studied by the oleatran paramagnetic
romonance method. Dokl.-AX SSSR 3.47 no.42867-869 D 162.
(MIRA 16 t 1)
1, Institut fizicheab3y khimii im. L. V. PiBarsbevokogo AN
UkrSM. Predstavlono akademikan M. 1. Kabachnikam.
(Quinbydrone) (Fbonazine) (Radjcals(Chexistz7))

GRAGEROV ask Pet--4-,%- TITOVA, N.M., red.izd-va; TURBANOVA, N.A.,
tekhn. red.
(Isotopes in the study of chemical reactions] Izotopy lzu-
chalut khimicheskie reaktaii. Kiev, Izd-vo Akad. nauk USSR,
1963. 65 P. (MIRA 16:4)
(Isotopes) (Chemical reactions)

-- GR&GEROV, I. P. I LEVIT, A.F.
Nechanim of coddation of diphenyl mlflde by Caro's acid.
Zhur'.A.Iffiis. 33 no.2043-5" F 163. (MMA 1632)
1-0 Institut fisicheskoy khimii imeni L.V.Pisarzhevokogo AN Ukr6SR.
(Phenyl milfide) (Peroxymonoeulfuric acid)

GRAGEROVp LEVIT, A,F,
.Isotopic exchange of ladaw--aM iodo compounds vith H20M*
Zhur.ob.khim. 33,no.2t544-U-163. (MMA 16s2)
1. Institut fWcheskoy*ktd:mJi imeni L.V.Pisarshevokogo
AN UkrSSR.
(Iodine compounds) (Oxygen isotopes)

GRAGEROVO I.P.; TURKINA, M.Ya.
....................
Isotopic and mass-opectrometric method of investigating the
mechanism of homolytic reactions in solution. Fart 4: Reaction
of iodobenze6a with magnesium and sodium. Zhur.ob.khim. 33
no.6s1901-1907 Je 163. (MRA 16:7)
1. Institut fizicheakoy khimii inani, L.V.Pisarzhevskogo AN UkrSSR
i Gosudarstvennyy institut prikladnoy khimii.
(Benzene) (Radicals (Chemistry)) (Deuterium compounds)

GRAGEROV, I.P.; TURKINA, M.Ya.
Isotopic and mass-spectrometric method of investigating the
met@anism of homolytic reactions in solution. Part 51 Thermal
deco!zOosition of diazonium salts and Gomberg-Bachmann reaction.
Zhur.ob.khim. 33 no.6:1907-1910 Je 163. (MIRA 16:7)
1. Institut fizicheskoy khimii imeni L.V.Pisarzhevskogo All UkrSSR
i Gosudarstyannyy institut prikladnoy khimii.
(Diazonium compounds) (Deuterium compounds) (Radicals (Chemistry))

GRAGEROV, I.P.; TMINA, 14.Ya.
Isotopic and mass-"etrometric method of investigating the
mechanism of homolytic reac:tions in solution. Part 6: Photolysis
of dipheny1mercury,.methyl iodide, and ethyl iodide. Zhur.ob.khim.
33 no.6:1910-1916 A .163. (MM 16:7)
1. Institut fizicheskoy khimi-i imeni L.V.Pisarzhevskogo AN UkrSSR
i GosudarstTennyy institut prikladnoy khimii.
(Radicals (Chemistry)) (Deuterium compounds) (Photochemistry)

GRAGEROV, LP LEVIT, A.F.; ZONOV, N.A.; TURKINA, M.Ta.
Benzene oxidation machanisa studied by means of isotopes and mass
spectroscopy. Dokl. AN SSSR 150 no.1:109-112 Yj 163. (MR& 16:6)
1. Inatitut fizicheskoy khimii im. L.Y.Pinarzhevskogo AN UkrSSR i
Gosudarstvennyy institut, prikladnoy khimii, Kiyev. Predstavleno
akademikom,M.I.Kabachnikom.
(Benzene) (Oxidation) ..(Csotopes) (Mass spectrometry)

GRAGEROV, Isaak Petrolodch, doktdr khim, nauk, otv. red.;
"!@'PWdorovna; LUNENOK-BURPAMIA, Valentina
Arsentlyevna; SHTULIMAN, I.F., red.
Aleksandr Illich Brodskii, Kievp Naukova dumkap 1965.
39 p. (MIRA 18:10)

GRAGEROV I,F,; CHIZHOV, B,V,
Study of the mechanism of homolytic reactior-.in solution by
.the isotopic and mass spectrometry methods. Part 7: Properties
ofgc -naphthyl and p-diphenyl radicals. Zhur.org.khim. I ro.3:578-
Mr 165,. (MI RA 18: 4)

-7-4 fTfm F(c/'
A :054 IM AP5015773
i LOV R
of ".he miechanism of hamG!,y+-ic macttors In G@,Ii 1 DrF '-e 15 t J4@e
-@,@zic c me 1,; h odB .o. ?roperties of benz,,11 and c7c!,.@hexyl radlcalB
ov6hGr, Zj2twnal cwganicheakoy khimii, V. 1, no, 5, 1965, 8-58-843
I TA CS :hcoalytic reaction, homolytic reacticti mecn i m, ot n,
ar- 5 Is c@x- solutio
berzy! radicaI property, cy,:Iohex-
aerie solition, hea ZYC on,@Xak,
ABSTRACT: The behwiorcC yl and eyelohexyl radical.- ir, solutions o-' hefk-.-f ben.*
cy'@Iohexane, a-deuteronaphthalezie, an@!
P(7
ted

ACCESSION HR? AP5013773
hyd-rogenate the ayclohexadienyl-type radicals formed in the procs-2gs, Rad M-,duce
vi, i ndi ca -
tolueres'. 2) the production of th,@ i;: qz
b,@u7.71 r-id-ica.Ls part@,,,i-,ate
f Ln the h2avy benzene med-ium of -Iiph-nyl-methane with a --haract-eristJc iso-!
topic composition, dependent cn the dispropartionatiort of isotoigtc Varieties CLE 1.
cjIscl, --;I\/-
--in the source of diri-,Pnyllmethanf@, the
tl%j
X.
T
"i -,.zK
iW
A
MUM, Q
R
IN - ill INIMARMWt P - -Mazi

Cc rd
gpa;g@,
-;3n4

GRAGEROV, J.P.; CHIZHOV, B.Va
Isotop.i,c and mass spectrometric D'OthOds for the study of the
mochanism of homolytic reaptiona in solution. Part 9: Certain
reactions of ob-naphthyl diazonium and p-diphenyl diazonium
chlorides. Zhur. org. khim. 1 no.7:1264-1268 J1 165*
(MIRA 1833a)
11 Institut fizicheskoy khimii imeni L.V.Pisarzhevskogo IN
UkrSSR.

ALEKSANKINP M,M.; CIIIZIIM"p B.V.; GOLIDENFELID, I.V.;z_qf@hGMZOV, I,P,
MuBs opectromebrio and Isotopic method of studying the
mechanism or hovolytic reactions in a solution. Part 10i
Reactione of iodobenzene, A-itdonaphthalhneo p-iodobiphenyl,
and benzyl chloride with magnesium* Zhur. org. khim. I
no.11:1909-1914 N 165. (MIRA 18112)
le Institut fisichookoy khimii imani L.V. Pisarshavskogo AN
UkrSSR. Submitted December Up 1964,

GELLER, B.A.; NEYMARK, I.Ye.; RUBANIK, M;Ya.; POLYAKOV,
M.V.; RUSOV, M.T.; DAIN, B.Ya. REUSHEVA, A.F.; STAAZHESKO,
D.N.; LUNENOK, V.A.; ROYTFR,.V.A.; SULIMA, L.V.; FOIENKO, A.S.
Alekeandr Illich Brodskii, 1895- ; on his seventieth birthday,
Zhur. fiz. khim, 39 no.6:1540-1541 Je 165.
(MIRA 18:11)

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GRAGEROVA, R. B.
"Mechanism of protective Characteristics of the skin in subcutaneous
tumor transplants." Medych.zhur. 20, No.4, 10,50.
Monthly List of Russian Accessions, Library of Congress, August 1952. Unclassified.

KCRINIVA-ZYIIKOYA, O.P.; GRAGEROVA, R.B., kand.med.nauk
Bffect of testicular extract on the growth of a transplanted
carcinoma in a rabbit following intradermal injection. Kedych.
zhur. 20 no-5:82-85 '50. (MIRA 11:1)
1. 'A" viddilu patofiziologii institutu klinichnoi fiziologii in.
ikad. O.O.Bogomolltys AN URSR (direktor institutu i zav. viddilam
chlen-kor. AV URSR prof. R.Ye.Kavetelkiy)
(CANCIOR) (TISSUX EXTRACTS)

r'y- ///g ('?'@@v co//' , /@" 1-5 @
KARCHUI, P.D., prof.; AR-AGIIRQYA&-A-..B., kand.med.nauk; KOROLI , S.A.,
)mnd.biol.nauk
Interspecies specificity of antireticular cvtotoxic serum. l4edycho
zhur. 20 no-5:94-98 '50. (MIRA 11:1)
1. 71 laboratorii Antiretikulyarnoi tattotoksichnoi eirovatki
(zav. - prof. P.D.Marchuk) rnatitutu skeparimentallnoi biologii
patologii im. eked. O.O.Bogomolltsva Miniaterstva akhoront
zdorovlya URSR (clirektor - prof. O.O.Bogomoletal)
(ANrIRETICUIAR CYTOTOXIC SHRUM)

@-,rhe limmunalogical properties of cancer nucle;jr-otet@s.,
It. B. GraKtrova.. UchenyeZapiski Kier. Manch. lisledova-l
MOW. i Omkoi. Imt. 4, 55-6000M); Referal.
Diol. Kkiffs. 1955, No. 62,11-1flood serums of'
rabbits immunized against nudeoproteins from spontan,!,ous!
ta@nnnary Slarxd canccrs of inke, rat -1,1rcoxnas, and Rous
&,trcoma -reacted in the classical antigen-antibudy inanner
with thc salt exti, of. corresponding cancers and nortual
1sitirs,
t
- - - howeytr, a considerably highc: coucn. of the scruln
was required for the lattcr reaction. Nuelcoprottini, of
Brown-Pearcesarwina of rats producf-d speTific anapbylactic
reactions In exptl, animals after 'hey had been dciensitized
_pM!qjL!is_ucnucIeoprPttins. B.5
------------
7 _7

Gragerova, R. B.
Experimental studies of the Dossibility of cultivatini, virus-R@-e
formations of cancer of the human stomach in chick emb-n-os.
H terialy nauchnykh konferentsii, Kiev, 1959. 2MDT)
(Fievskiy Nauchno-issledovatellskiy Institut Epidprmiologii i Hikrobiologii)

Grar?erova, R. B., and Barshteyn, YU. A.
Additional to the morphology of the chorio-aliantoic menbrane of chi@@k
oribryos while thro@uth the latter the extract of a cancerous tljmor
of the stivine;-1. 06
Mornhological nharacteristics of changes in the 14-v,@r of chick enbryos,
on the chorio-allantoic Tie-hranc ol -i-.,hich, extract, of cancer.-)us tuilor roil
the stomach was rcssagod. V-4 ---1, 6 @
"aterialy nauchnykh konferent@ii, Kiev, 1959. 28)6p-
IXievskiy Nauchno-issledovatel'skiy Institut -Epidf-@Aologii. i ;'.akrobiologii)

GgAGEgOyA, a..j. and BARSHIM, YU. A
Additional to the morphology of the chorio-aliantoic membrane of chick
embryos while passaging through the latter the extract of a cancerous
tumor of the stomach. p 262
Morphological characteristics of changes in the liver of chick embryos,
on the chorio-allantoic membrane of vhich, extract of cancerous tumor
from the stomach was passed.
Materialy nauchnykh konferentsii, Kiev, 1959- 288pp
(kievskiy Nauchno-issledavatellskiy Institut Edidemiologii i Mikrobiologii)

GRLGEROVAO R.B. (Hraherava, R.B.];' SHURIYAB, O.S.
Sixtieth birthday of Nina Borisovna Medvedeva corresponding member
of the Academy of Sciences of the Ukrainian S.S.R. Fiziol. zhur.
[Ukr.] 6 no..3:425-d*26 MY-Je 160. (MIRA 13:7)
(WMEMAq NINA BORISGVNA9 1900--)

GRAGEROVA, R.B. (Kiyov, ul. Pushkinakayaj, 11., kv.20)
Antigens from cancerous tumors of the stomach in man. Vopo
onk. 7 no-503-59 161. (MIRA 15:1)
1, lz laboratorii atiologii opukholey (zav. - deystv. chl,, AMN
SSSR A,D. Timofeyevskiy) Kiyevskogo instituta epideniologii i
mik:robiolo ii (dir. - kand.med.nauk S.E. Terekhov).
@STCMACS-CANCER) (ANTIGENS AND ANTIBODIES)

GIUGEROVAP R.B.; CHALAYA,, M.P.; ASHMLRINL, O.K.
I - ''.- I-'-
Detecting the oncogenic factor in human gastric cancer
extracts by means fo cultivation in tissue cultures.
Vop. virus. 7 no.3:316-321 My-Je'62. (MIRL 16:8)
1. Laboratoriya, etiologii opukholey Kiyevskogo instituta,
epidemiologii i mikrobiologii.
(STOMACH-CANCER) (TISSUE CULTURE)
(VIRUSES)

0 IN, i"%-. -%J.
RRAHIROVA, R.S.
. .
Possibility of nentraliving the uUk factor by a specific immune serum. Mdych.
zhur..22 no.4:30-32 '52. (PTAA 6--10Y
1. Instytut klinldhnoyl f1slolohlyi in. akad. 0.0.30homollteya AN UR".
(serum) (Kilk) (Tumors)

IMAGHICIU. 0.; POP, A.; GRAGRICIU, GI.; ANDDR, G.; KARGnUANU, T.; GOTARQ, K.;
Chronic dinitro-ortho-cresol intoxication in phytosenitary workers.
Rumanian M. Rev. 2 no.2:21-2@ Apr-June 589
(INSWTICIM, pois
dinitro-o-cresol, in phytossnitary workers, review)
(FMICIIM, polo.(
same)
(OCCUPATIML DL93ASIN
dinitro-o-cresol pols. in phytosanitary workers. review)

GRAGIC, Djordje, pukovnik dr.
Medical cadre and instuction under partisan conditions; considera-
tions based on experiences from the National Liberation War of
Tugoolavi&. Toj. san. pregl.. Peogr. 11 no.9-10:403-410 Sept-Oot 54.
(MEDIC M,'MILITART AND NAVAL, education
Yugoel., train. of personnel)

GRAGIEV, N.
"Biothermal chambers" (P-13)
(Ifinisterstvo na stro*ezhite
blagoustroistvoto, i 111aushria
APIMITIR- T MI I MnITEMSTV0
0
i putishtata, Ministerstvo na komnalroto stopanstvo i
teklmichesId.1a suiuz) Sofiya vol 3 "o 11 1953
SO East European Accessions List Vol 2 No 7 Aug 1954

1. GRAOINA9 F, C,
1
2. USSR (600)
4. Afforestation - Accounting
7. Improving shelterbelt forestry accounting in machine-tractor Stations and
collective farms. Los i step' 5, no. 1, 1953.
9. Monthl List of Russian Accessions, Library of Congress, MBY -1953, Uncl.

TEWAKINA, A.Ye.; RABINOVICH, M.S.; ZHDANOVICH, Yu.V.- STIRUKOV, I.T.;
KONDRATIYP"VA, A.P.; BUYANOVSKAYAt I.S.- SHNIYERS0112 A.H.;
f
GRAGINSKAYA, P.S.; LRUZHININA, Ye.N.
Alpha-aminobenzylpenicillin (&Wicillin) and its microbiological
studies. Antibiotiki 9 no-5:.@6,-392 My 164. (MIRA 18:2)
1. Vaesoyuznyy nauchno-issledovatellskiy institut antibiotikov.,
Moskva.

GRAHEK, Branko, Potpukovnik mr. ph.
Review of activities and function of Drug Control Laboratory
of the Tugoslav Military Medical Academy. Voj. san, pregl.,
Beogr. 13 no.9-10:477-480 Sept-Oct 56.
(LABORATORIES, MEDICAL,
Drug Control Laboratnry of Tugo9l. Military Had.
Academy, activity & funct. (Ser))
(MICINN, MILITART AND NWAL
same)

Gamics, Agnes 1933-1963
WEATHER FORECASTING DECEASED
lz
1964

GRUGS, Istvan
Climatic changes. Idojarao 66 no./+.-231+,238 JIL-Ag 162.

GRA TY, A. L.
Dilution turbidity test In hepatic d1seanas. Med.letopiali 41
no.10:1038-1047 D 149, (CLML 19:2)
1. Of the People's Hospital dedicated to Jews Fallen for the
Freedom of Bulgaria (Read -- T.Tranen, M.D.), Internal Diseases
Division (Head - Docent T.T.Tsonchev, M.D.).