SCIENTIFIC ABSTRACT GITIS, E. - GITLEVICH, A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000515210016-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 26, 2002
• Sequence Number: 16
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KRAYMER, Leonid Pavlovi,:h; GiTIS, E.I., rettionzont; CNIVIII-A', A.F.,
rod.
[High-speed ferrornagnetic rrrem(,ry device.-] ByotroAeist"-
iushchie ferroniagnitnye zajomLlnaiuBhchle ustroist-va. Yo-.
skva, Energiia, 1964. 370 p. (M iA 17: 12)

GITIS, Ewnanuil Isaakovich. Prinimall uchastiye: SAPIOYLENKL), V.I.,
kand. tekhn. nauk; BALTRUSHEVICH, A.V.? kand. tekhn. nauk;
ZHDANOVY G.M., prof., retsenzent; 1C:AYZMER, L.P., kand.
tekhn. nauk, retsenzent; FLID, Ya.l., kand. tekhn. nauk., red.
[Automatic control of radio systems; electric and a,'ptomatic
control of radio systems] Avtomatika radioustanovol:; elektro-
radioa-vtomatika. Moskva, Energiia, 1964. 631 p.
(141-AA 17:11 )

!ACCESSION NR: AP4037467 S/0146/64/007/002/0082/0089
AUTHOR: Gitis, E. L; Pronin, Ye. G.
TITLE: Generalized characteristics of a multichannel semiconductor converter
of voltage into a code with digit -order coding
SOURCE: IVUZ. Priborostroyeniye, v. 7, no. 7., 1964, BZ-89
TOPIC TAGS: converter, voltage code converter, semiconductor voltage code
converter, multichannel converter, automatic control
ABSTRACT: The method of generalized characteristics pdrinits selecting'the
kind of converter for specific conditions of application. The characteristics axe
independent of the degree of perfection of a specified scheme or design. Any
converter can be subdivided into two types of generalized units. (1) amplifier
units (triggers, differential and piilsed amplifiers, switch controls, etc.), and
(Z) analog.units (voltage switches, saw-tooth oscillators. comparison circuits,
Card I

!ACCESSION NR: AP4037467
etc.). The number of units of a multichannel converter is given by:
N - N,,, (m+n+Z) + N.,(m+Zn+4). where N,. and N,,,, are the number of active
and passive elements in an analog and amplifier unit. respectively, m is the
number of input channels, and n is the number of digits in the output code. The
time of the full cycle of conversion of all-channel voltages is given by:
T - m -r [k(3n*-Z) + (7n+Z)j .where is the amplifier-unit time constant
1 and kT... The above generalized theory is illustrated by a numerical
example of a 10-channel converter of voltage into a 10-digit code. Orig. art.
I has: 4 figures, 3 formulas, and 2 tables.
!ASSOCIATION: Moskovskiy aviatsionny*y institut (Moscow Aviation Instituta)
SUBMITTED: ?.IFeb63 DATE ACQt 05Jun64 ENCL9 00
SUB CODEt DP.'. No REr SOVs 004 OTHERt 000
Card. ?./?..

,..ACCESSION NR: AP4042496 SIO 103/64/OZ5/007 /110411113
AUTHOR: Gitis, E. I. (Moscow)
TITLE: Gray code counters
SOURCE: Avtomatika i telernekhanika, v. Z5, no. 7, 1964, 1104 -1113
TOPIC TAGS: counter, binary counter, cyclic code, binary cyclic code counter,
Gray code counter
ABSTRACT: The Gray code to analyzed, and the rules for converting a conven-
tional binary code into the Gray code are established. This logical equation
--f-describes the trigger action in-a Gray-code counter adding a pulse:
i
Ek = e*Tk_, Ti, where E, a I when a digit changes in the k-th digit place and
Ek Z 0 if the digit does not change in the k-th place; T,, V_k is the code element;
e. means the arrival of a pulse. A similar logical equation describes subtraction.
"Crtrd'-Z

ACCESSION NR: AP4042496
These equations are used to explain the structure of such known codes as those of-
A. Fischman, G. D. Hulot, and certain Russian authors, and the modifications
suggested by the author. Orig. art. has: 5 figures, 20 formulas, and I table.
ASSOCIATION: none
SUBMITTED: 28Feb63
I SUB CODE: DP
ATI) PRESS: 3082 ENCL: 00
NO REF SOV: 004 OTHERI 005

ACC NR. AP60250654 SOURCE CODE: UR/0413/066/ooo/013/0107/0107
iNVENTOR: Gitis, E. I.; Bergellson, M. N.
ORG: None
TIT_-_~': An arithmetic unit for performing the operations of addition and subtraction
in self-checking cyclic code. Class 42, No. 183464
SOURCE: lzobreteniy,., promyshlennyye obraztsy, tovarnyye znaki, no. 13, 1966,-107
TOPIC TAGS: arithmetic unit, cyclic coding, flip flop circuit
A3STRACT: This Author's Certificate introduces an arithmetic unit for performing the
operations of addition and subtraction in self-checking cyclic code. The device con-
~ains flip-flop registers for the first and second numbers with recording and set
circuits, a circuit for cyclic carry, determination of the resultant sign and digital
nework overflow check, and circuits for monitoring progress of the operations. To
s;.Mplify the device and increase its speed, each i-th digital place except the flip-
flops of the registers for the first and second numbers contains two modulo 2 adders,
a circuit for carry to the following i+l-th digit and a diode. The d-irect (inverse)
outputs of the flip-flops for the first and second numbers are connected to the f1rat
direct (inverse) inputs of the first and second adders respectively. Connected to
the second direct (inverse) inputs of the first and second adders respectively are
Card 1/3 uDc: 681.142

ACC NR%
the direct (inverse) ouputs of' the first and second adders for the preceding i-i-th
digit. Zhe inputs of the carry circuit are connected to the direct outputs of the
adders for the given circuit and to the carry output of the preceding i-l-th digit
,6iaich is also connected to the counter input of the flip-flop for the first number ofi
tne given i-th digit, and through the first delay line to the counter input of the
flip-flop for the second number of the following i+l-th digit. The direct outputs of)
zIne adders for the most significant digit are connected to the first inputs of the i
first and second monitor circuits. The second inputs of these monitor circuits are
connected to the sign digits of the first and second numbers respectively. These
inputs are connected together with the,carry output for the most significant digit
to the circuit for determination of the resultant sign, overflow check-and cyclic
carry. The cyclic carry output of this circuit is connected through the second and
third delay lines to the counter inputs of the flip-flops for the first and second
digits of the second number and to the first input of the first collector circuit re-
spectively. -,ne second input of this collector circuit is connected to the control
signal source, while the output is connected to the inverse inputs of the adders fIOr
~ae most significant digit. The outputs of the second adder are connected through
the second collector circuit and the fourth delay line to the reset terminals of all
flip-flops in the register for the second number and to the first inputs of the di-
odes for a.!! digitts. connected to the second inputs of these diodes exe the direct
oatputs of the corresponding flip-flops in the register for the second number. The
diode outputs are connected to the counter inputs of the correnpondin6 flip-flops 4n

ACC NR; V36025651,
t"ac re6i,-.ter for the first number.
1--flip-flops in the register for the first num-
A- ~'~ I
ber; 2---;fIip-flops in the register for the second 4!; _1
_IUMUer; --first mod 2 udder; 4-second mod 2 ad- 17 A
der; 5--carry circuit; 6--diode; T-10--first, 16~1
J-
second, third and fourth delay lines respectively; r1l
cuid 12--first and second collector circuits;
13 aid 11+--first and second monitor circuits; 15--
'4 PP
rcult for sign determination, cyclic carry and jo jo X
diZital network overflow check; 16--cyclic carry-
output-, 17 and 18--direct and inverse flip-flop outputs; 19-21--flip-flop set, reset
ana counter terminals respectively; 22 and 23--direct and inverse outputs of mod 2
adder; 2,4 and 25-first direct (inverse) addoer input; 20' and 27--second direct (in-
verse) adder input; 28--carry circuit.output; 29--reset terminal of flip-flops for
thle first n-x--ber; 30--terminals for recording in the register for the first number;
31--teminals for recording in the register for the second number; 32 and 33--input
terminals for the'sign digits of the first and second numbers; 34--control input.
SUB CODE: Oq/ SUBM DATE: O3ju165
CQrJ 3/3

AC~ ~NR.-'~ AF6oi6823
SOURCE CODE: uR/oi)~4.6/66/oi2/oo2/oi45/ol5gI
AUTHOR: Gitis, M. B.; Mikhaylcrv, 1. G.
ORG: Leningrad State Univer~ity (Leningradskiy gosudarrtvearvy univercitet)
TITLE- ProWation of sound'in liquid metals ~feview)
SOURCE: Akusticheskiy zhurnal, v. 12, no. 2, 1966, 145-159
TOPIC TAGS: sound propagation, molten metal, ultrasound absorption, acoustic meau
ment, acoustic speed, temperature dependence, compressible fluid, viscous fluid
ABSTRACT: This is a relew article dealing with methods of measuring the 7~eloc a
absorption o asound in liquid metals, with the experimental results already ob-
tained by thes_e_m_eTFo_cTs_, and with the data that can be extracted from these results
in order to obtain information on other physical properties of liquid metals aver a
wide range of temperatures. A summary table listing the speed of sound and its tem-
perature coefficient for a large number of metals is presented. On the basis of the
results a distinction can be made between normal metalsp in which the radical re-
alignment of structure terminates at the melting point, and metals in which the shor
range order structure experiences changes in the liquid state. These include tin,
bismuth, and gallium. It is concluded that in molten metals, in spite of the relati:
simplicity of the structure, the speed of sound behaves in a complicated manner with
increasing temperature. The compressibility of the molten metal is a quantity sen-
sitive to the structure. Inasmuch as liquid metals consist of spherical symmetrical
Card 1/2 uDc: 534.221: 669.o17

L 36536-66
~CC_N_R' Ai~6oI6823
simple particles, a study of the compressibility and the speed of sound leads to in-
formation on the interatomic forces between them. The maximum speed of sound and
consequently the minimum of compressibility can be due both to the formation of a
second close-packed structure in the liquid metals, and to a temperature variation
of the number of carriers. Measurement of the sound absorption in molten metals is
the only source of data on the volume viscosity, but the determination of this quan-
tity calls for comprehensive study of both acoustic and thermal characteristics of
/the same samples of molten metal. Measurement of sound absorption in a broad tem-
perature interval may yield valuable information on the influence of different
structural rearrangements on the kinetic coefficients of the liquid metal. Orig.
art. has: 12 formulas and 2 tables.
SUB CODE: 2o/ sm DATz: igNov65/ oRiG my: o28/ oTH Ru. va6
C,rd 2/2,t-,,, /-

GIVIS sent
Zffect of cllaute and weather on the incidence of pnettmoala and
its course during the year. Gig. I son. 22 no.2:58-60 F '57
MRA 1o:4)
1. Iz L'vovskogo Instituta spidemiologii. mikrobiologii I gigiyeny.
(PNZUMONIA, opidemiol.
in Russia, off. of climate & weather on Incidence &
course)
(CLIMATE, off,
o.n.incidence & course of pneumonia)
(VUTMM, off.
same)

GITIS, I.I., dotsent, Jcand.mod.naiik
Dynamics of the climate of Lvov over a period of many years.
Gig. i san. 24 no-7:9-15 JI '59- (MI-RA 12:9)
1. Is Wvovskogo meditainakogo instituta.
(CLI1WT'JC
off. of urban develop. on climato of district
in Russia (Rna))

GNU, I.I., dotsent
Nobile observation crews In making hygienic study of the climte
of a large city. Gig.i san. 25 to.lt87-89 Ja 160. (HIPA 13:5)
1. Iz L'Yovskogo meditsinskago instituts.
(AIR PaUMION)

GITIS, I.I. (L'vov)
Prevention of bursitis among miners. Gig. trude i prof. zab. 4
no. 7-60-61 Tl I 6CL (MIM 13 -.8)
1. Meditsinskiy institut.
(LVOV-VOLYN BASIN-COAL MIN~~-DIS.*-,'.'-6~Z 111D HYGf~,KE)
(BUFWTIS)

GITISl I.I. (Hitis, LI-b dots.
Dynamics of catarrhal diseases of the respiratory organs among
WtUdren in Lvov. Ped. a1wsh. i gin. 22 no. 1:33-34 160.
(MIRA 13:8)
1. Llvovskiy meditsinskiy institut (direktor - prof. L.N.
Kuzimenko).
(LVOV-PZ,SPIRATORY ORGANS-DISEASES)

KAZANSKIY, B.Az; DOROGOCHINSKIY, A,Z,; ROUMART, MJ,; GITISP K.M.;
LYUTER, A-V,; MITROFANOV, 14-G,
Effect of the length of an alumin&-clxbmiar-potassium
catalyst layer on the aromatization of n~heptane,
Kin.i kat. 4 no.2:315-318 Mr-Ap s63. (MU 16:5)
1
1. Institut organictieskoy khimii UI SSSR imeni N.D.Zelinalcogo i
Groznenskiy noftyanoy nauchno-is:iledovatellskiy institut.
(Heptane) (Aromatization) (Catalysts)

ROZENGART, M.I.; GITI�,_, LM.; KAZANSKIY, B.A.
DeveloFnent of an a2umina-hrome-par~r-Esium f,r t!:e
dehydrocyclization of paraffin hydrocarbons. Pleft-akiin-L!i '
no.11:406-412 My-Je 164. (1,-IRA 18:2)

j-,e an alkali
cllro,moi catialwjI. for th(.
carbor s. Ne f te kh imil J a 5 no 1: 1

ROZENGART, M.I.; POLKOVNIKOV, B.D.; POLININ, V.L.; TABFR, A.M.; GITIS, K.M.
Aroffiatizing capacity of boride catalysts of platinum group metals.
Izv. AN SSSR. Ser. khim. no.5:919-922 165. (MIRA 180)
1. Institut organicheskoy khimii im. N.D.Zelinskogo AN S,%qR,.

13996
S/05 62/000/004/002/017
B101YB186
AUTHORS: Gitis, 1M. B., Mikhaylov, I. G., Khimunin, A. S.
TITLE- Apparatus for measuring the sonic velocity in liquid metalis
and melts
PERIODICAL: Leningrad. Universitet. Vestnik. Seriya fiziki i khimii,
no. 4, 1962, 52-55
TEXT: An apparatus working or, the principle of electroacoustic feedback,
able to measure ultrasonic velocity with the transducers in fixed positions
is described here. Instead of the ultrasonic propagation velocityr the
pulse repetition frequency is measured, i.e. the ultra-sound which has
passed the test medium, is amplified, shaped, and again starts up the master
pulse generator. The ultrasonic velocity is determkned by c=d/(l/f + 'ry),
where d is the distance between the vibrators, f the pulse repetition
frequency, x z the total electric and acoustic delay. To allow operation over
a wide range of temperature the measuring cell has two delay rods. To
eliminate the effect of the temperature Eradient occurring in the delay rods,
Card 1/2

3/0 5 4/6 2 /OGG /00 4/00 210 17
Apparatus for mieasurint~'the.., B101/B166
the ultrasonic propagation velocit., is Measured not only, pasSin6 through
the system but also in the reflection from the rod-fu-iion interfaces.
c - 2d'f -, f.-
, /(2f f ~f I ), where f and f i,; I.-Ke p,.~Ise repetition
1 21 1 2 1 2 1 2
Irequency in the two rods. The distance d is calibrated by a liouid of
'-nown sound conduct4vit,,-. The pulse Cenerator de'ivers negati f
r
. - Ive pulses 0
3 iksec duration, 150 v amplitude, 3tartin6 up a shoqk Eenerator. Me a s ur e -
ment3 are made with the precisely fixed frequency of 5 AIc/s(IC. The delay
rods consist of fine-,-rained 1.Y18H97- (1Kh18N9T) steel, A check of the
ultrasonic velocity in mercury between -30,.2 and +700C shcwed ~aod agreement
with the data found by 0. J. Kle~,pa (Ultrasonic velocities of sound in some
liquid metals. Adiabatic a;,.d isothermal compressibilities of liquid metals
at their meltin6 points. Journ. Chem. Phys., 18, 1331, 1950) ana
E. B. Freyer, J. C. Hubbard, D. 7.". Andrews (sonic studies of the physical
properties of liquids. Journ. Amer. Chem. Soc., 51, 759, 1929). There
are 1 figure and 1 table.
SUBMITTED: Ilay 22, 1962
Card 2/2

I -A
- - - - - - - - - -
L 7868- /EED I
EWT(1)/EWT(m)/EPr-(n)-2/~VP(t)/I~9P(b) -3A TC m IJP JD' WW
P-O-HrO 66~4Ri~7~
ACC N& AP5028046 SOURCE CODE UR/0046/0 0
AUTHOR: Gitis M B. Mikhaylov, 1. G.
Y q I 5r S--
ORG: UninLrrad State University (Leningradskiy goandarstvennyy uaiversitet)
TIT LE: The speed of sound and the compressibility of some liquid metals
SOURCE: Akustichesidy zhurnal, v. 11, no. 4, 1965, 434-437 1
24 qq
_p% c tr
TOPIC TAGS: silver, lead, tin, antimony, bismuth, liquid metal, acoustic s Le el c ic
conductivity, metal property
ABSTRACT: The article reports on the measurement of the speedof sound In the following
liquidmetals: silver~-6pper~'leadl~ltiir,?bismuth,~Ud antimony'lii abroad tempprature range.,
depends
In liquid Eilver and coppir, in the emperature range up to 1400C, the speed of sound
linearly on the temperature. In lead, tin, bismuth, and antimony the temperature-dependencle
of the speed of sound and compressibility Is more complicated. la lead, fa~ example, starting
with a temperature of 900C and above, the temperature coefficient increases smoothly. In
antimony, on the other hand, the speed of sound attains a distinct maximurn at $50C. There 'as
a correlation between the character of the temperature-dependence of the speed of sound and
the electric conductivity of the metals investigated. OrIg. art. has: 4 Rgarea.
SUBCODE: MM,GP/SUBMDATE: 3OMar65/ORIGREF: 008/0THREF: 004
I Card 1/1 ....534.2 2:046.3
UDC

IT/'0jP(+.)/7PT
1; 31522-66 - - -a'-ra)1FWT(M)/FTr(f in
ACC NK' AP 007993 SOURCE CODE: UR/0046/66/012/001/0017/0021
AUTHOR Gitis, M. B. ; Mikhaylov, 1. G.
ORG: Leningrad State University (Uningradskly gosudarstvennyy universfl]et)~
TITLE: The r'elationship between the velocity of sound and electrical conductivity In
liquid metals6
SOURCE: Akustlcheskly zhurnal, v, 12, no. 1, 19661 17-21
TOPIC TAGS: liquid metal, ultrasonic velocity, electric conductivity, metal property
ABSTRACT: Elsewhere, the authors (Skorost' zvuka I szhimayemostil nekotorykh zhidkM
metaflov. Akustich. zh., 1965, 11, 4, 434-437) desc[4bed expe on,~~e measurement
.f,ln) Tts
of the velocity of propagation of ultrasound In liquid Ae, Cul,' Pb'~ Sni' and Sb. In the present
I -
article the authors pr n! IgatioiF-of 0trasonte vel&ities In several other
e f at%on 4e iyest
molten metals, i.e., T17M Ga Zn Cd TeYIA correlation of the electrical and the
~ and
acoustical data of the observed in the temperature range from the melting
point to 950C. An explanation of this phenomenon Is presented, based on the Mott theory.
Orig. art. has: 4 figures, 1 table, and 3 formulas.
SUB CODE: 11, 20 / SUBM DATE: 06Aug65 / ORIG REF- 008 / OTH REF: 003
Card 1/1 zc_ UDC: 534.22

ACC N;Z, ~26a214713 SOURCE-CODE;- UH/0413/66/0001011/0094/&~qL
Zhuravell, V. I.; Minakov, V. I.; Bobrov, V. T.; Dimitraki, P. N.;
forenko, 7.h. G.; Budenkov, G. A.; Gitis, M.%.
0,-,G: None
T:='~: An ultraaonic PUIGC-Ghadow Immersion flaw detector. clans 42, No. 1.8239o
[..:inoL:nccd by the All-Union Scientific Research Institute of Nondestructive Hathods
for Xaterial Quality Control (Vresoyuznyy nauchno-ioGledayatellakLy inatitut ner&z-
nushayushchikh metodoy kontrolya kachestva materWov))
izobreteniya, promyshlenny-fe obraztsy, toyarnrye znaki, no. u, 1966, 94-
TO?IC TAGSt flaw detection, ultrasonic flaw detector, quality control
;ZSMACT: This Author's Certificate introduces: 1. An ultrasonic pulse-Gh&dow im-
=erzion flaw detector which contains an ultrasonic probe unit, line scanning mtchan-
J*r;~, oscillator and ultrasonic amplifier. The unit in designed for in--reaGed pro-
ductivity in checking parts of complex shape. The installation incorporates an elec-
troz.ic unit which generates a control signal after the ultrasonic probe unit passes
beyond the outline of the part being chocked. This signal controls the line scanniag,
mechanism and temporarily disconnects the receiving head from the amplifier. 2. A
modification of this flaw detector in which the electronic unit is made in such a
-Card--1/2 LM 6ZOJ19.%(6.C8

-ACC NR, AP65M473
way that. when there is a single pair of ultrasonic probes in the installation the
receiver head ir. disconnected from the amplifier during the period when the probe
urit is returning to the article being checked, 3. A modification of this flav do-
.ector in which the electronic unit is made in such a way that when there are two
pairs of ultrasonic probes located one behind the other along their line of motion
the inr
stallation, the receiver head disconnected from the amplifier Is the one
which first passes beyond the outline of the part being checked. 'This receiver head
is connected when the second pair of probes passes bVood the outline of the part on
the return travel of the probe unit.
SUB CODE: 09, 13/ SUBM DATTE: 07Dec64
C.rd 2/2

GITIS, M.I., inzhener.
Yloat gauge for determining the volume of bitumen and tar in a
cauldron. Rats.i isobr.predl.v stroi. no-57:9-10 '53. (KLRA 7:2)
(Volumetric aq3aratue) (Bitumen)

prof.; KASHKAREVA, A.P.
Arteries and veins of the sternum. Khirurgiia 34 no. 12:55-60 D '58
(XIA 12:1)
1. Iz kafedry operativaoy khirurgii i topogr,,ficheakoy anatomii (zav.
prof. M.K. Gitis) Omskogo meditainskogo instituta imeni M.I. Kalinina.
(STIMM, blood supply
arteries & veins (Rus))

Expenses should be planned correctly. Sov. torg. 35 no.12:29
D 161. (I-OMA 14-n)
1. Nachallnik planavo-finansovogo otdela Goradskogo upravleniya
torgov1i, g. Chelyabins~!.
(Restaurants, lunchrooms,, etc.-Accounting)

J& ;4" , .
GITIS, S.S.; GLAZ, A.I.
Reactions of aromatic nitro compounds. Part 2: Reaction of
trinitroanisole and trinitrophenetole with alcoholates. Zhur.
ob.khim. 27 no-7:1897-1900 Jl 157. (MIRA 10:10)
l.Dnepropetrovskiy gosudarstvennyy universitet.
(Anisole) (Phenetole)

t; ~ S. F'. , 61-, .". 1.
.59
ot' Az-~tpa~.io Nitrocornp,)unds (Reaktnii aromatiche:,kikh
nitrr,coyedineni.v)
ITT. Nvw 7ynthPsis M"thod of the Alkyl-Ethers of 2,4-
Diniti-ophenol ITTI Novyy spo.-..~b poliicheniyu alkillnykh
efirov ~,4-dinjtrofenola)
p~,HTC)DICAL- Zhurnal Obshchey KhJmii, 19589 Vol-, 28, Nr 5,
pp, il;34-1336 (USSR) '
AB'i".Ar,r: Complementary to the syntheses elaboraf.~_d in three different
ways by foreign scientists with resDect to tha 2,4--
dinitrophenclether (refA 1-5),,the authors recently showed
(ref 6) that the methoxy group in 2,4,6-tr.-initroaninolp car
be easily replaved by other alkoxy grotips. Starting from
this a number of investigations rere carried otit also with,.
2,4-dinitroani sole in ordrir to converl; it -into otner ether.,_
This conversion takes plhcr at., room temperature.
It is assumed that also irk t.h~ the reaction takes
p3ace accord-ing ko the mechartism proposed by thr- author!~
(ref 6). Thi s Nay .- the etbyl-n-propyl-, n-butyl-, primary-
C,-.rd 1/2 isobUL~11- and urLmarv iskl&mylpchers of 2,4--linitropheno"

- U/69
Reactions of' Aromatic N4-trocompounds.
!I!. New 3yritneais Met'nod or the Alkyl-Fthers of'
were obtained from ~, 4-di ni troan-i sole I:n good yieldr. It
is of int~_.rest that. Lhe inoi)ropylpther Cain noL be cbtaine:`
"0 .3 m ethod P-q the ot, 11 lri!O j V
prod)io, Is not decomprsed y w,~ter. .',pparently the ramifi,~d
,vr,.)up does not sert.1te nk-ir th~ M~~thoyv P~.roup
ozz,thopnaition. to the tiltro 6-roup, which itseLf
ej a
is in the p::,qitinrt .4; kbis excludes the pr-rib4lity of
diqplac~ment of the inethoxy group (see This meth,:d
-iven ~,v tne authors has its advantage compav.~d ti) those
rnentlor.pd in putiiieutions,. 'riir~ 2,4-dinitvophenol~thqrs are
obtu;rie,_( in pure t-r.vt~t-t; i m .,tato anti covre~;pnnd n1most.
comple%s~)Y to the Lv,.,ra other
'Ph*-.re Prc- tablri lr,i nr-~fprenres, I ~f whioh i.,; S-oviet,
N - L-11 0 o... ,, 1-3 k i
y posti,in vv t vennvy tin i vi-- rq t ~- t
f-D-Z Z2-0 V.~ tk State Universi tv)
4.

sov/79-28-8-5-/66
kUTHORS: Gilia-j. P. S. , Ualinovskiy, M. S. , Gla2, A. 1.
TITLE: Reactions of the Aromatic Nitro Compounds (Reaktsii aromati--
cheskikh nitrosoyedineniy) IV. The Re-Alkylation Reaction of
the 2,4-Dinitrophenol Ethers (IV. 0 reaktsii perealkillrovariiya
efirov 2,4-dinitrofenola)
PERIODICAL: Zhurnal obshchey khimii, 1958, Vol. 28, Nr 8, pp. 2262-2264
(USSR)
ABSTRACT: In this paper the re-alkylation of not only 2,4-dinitroanisole
is reported, as was the case with an earlier paper by the
authors (Ref 1), but also that of other alkyl ethers of 2,4-
dinitrophenol. In the substitution of one alkoxy group for
another the authors found it to be a regular occurrence that
the alkoxy group was displaced with a greater negative induction
effect. It was found that by re-alkylation the following com-
pounds can be obtained in good yield: 2,4-dinitroanisole from
the 0-oxyethylether of 2,4-dinitropher4ol; 2,4-dinitrophenetol
from 2,4-dinitroanisole; the n-propyl ether of 2,4-dinitro-
phenol from 2,4-dinitrophenetol; the n-butyl ether of 2.4-d-4-
Card 11/3 nitrophenol from the n-propyl ether of 2,4-dinitrophenol; the

SOV/79-28-8-55/66
Reactions o,- the Aromatic Nitro ComDounds. IV. The Re-Alkylation Reaction
of the 2,4-Dinitrophenol Ethers
primary isobutyl ether of 2,4-dinitroph--inol from the a-butyl.
ether of 2,4-dinitrophenol; the primary isoamyl ether of 2,4-
dinitrophenol from the primary isobutyl ether of 2,4-dinitro-
phenol. From 2p4-dinitrophenatol, howevt~r, 2,4-dinitroanisole
could not be obtained, and so forth. The alkoxy groups can be
arranged in the following order according to the strength of
their substitution effect: primary iso-C 5H11 0> primary iso-
C4H90) n-C 4H90> n-C3H7O> C2H5O> CE 30 >110CH2CH20. The series ~s
in complete agreement with the data on the strengths of alkoxy-
acetic acids (Ref 4). The reaction occurs at room temperature
over the period of one hour. Upon warm-Jng the solution a ccm-
plete saponification takes place with bhe formation of din-4trz.--
phenylate (Table 1). The constants of the solid and liquid
ethers obtained are given in table 2.
There are 2 tables and 6 references, 2 of which are Soviet.
ASSOCIATION: Dnepropetrovskiy gosudarstvennyy universitet (Dnepropetrovsk
Card 2/3 State University)

3 '~' 3 )
A jT HORS Gi-tJs.,.,,..4.,&.., Rapchinskaya, 5. Te.
T I T LE Reactions of Aromatic Nitro Comuou%ds. V. Re-etherification Gf
Al'-,,,I- and Aryl Ethers of 2,41-Dinitrophc-rcl
PERIODICAL: ZhArnal obshchej khimii, 1959, Vol 211, J;r 8, pp 21,'),:6-_-,64E (USSR)
r
ABST11ACT: As Gitis arid coworkers had -revioa3ly otat-_d 'Ref 1 the
substitution of one alkoxy-group for ano-her in the alkyl
ethers of 2,4-dinLtrophenol takes place in s'ach a -ray that t'-,,?
alkoxj group is displaced which exerts si hi,~her negative in-
dUCt4ve Lffect. It suggested itself to d~-tect thij pheno=enon
also in other composed alkyl- and aryl ethers, It was the pur-
pose of the present papper to obtain, by re-etherificatJon, the
3orr,::sponding alkyl- and aryl ethers of 2,4-dinitropbenol, and
to establish an order of the alkoxy- and aryloxy-e-,rcups in de-
pendence on their electrodonor properties. The synthese's in-
dicated that the glycol ether can only be obta'--ed from the
phenyl ether, the allyl ether from the phenyl- ard gly--ol ether,
the benzyl ether frora the phenyl-, glycol- and alkyl ether.
Card 1/3 Dinitroanisole is formed from phenyl-, ;lycol-, 11yl- and

Reactions of Aro..-,atic Nitro Compounds. V. Re-etherification SDV/79-2~-8---,1"z-;-
of Alkyl- and Aryl Ethers of 2,4-Dinitrophenol
benzyl ether. Farfuryl other can be obtained from all thf--se
ethers and also from the pri,iiary isoamyl -ether of' 2,4-dini~.ro-
phenol. The following gradation order of the alkoxy- and uryl-
oxy-groups can thus be established a=)rding to ti-.,e intensity
of the substituting effect;
-C Hi IO> n.-C 5H 11 o> Primary iso-C 4H90>
OCH Q>Primary iso 5
n.-C3H70) C 2H50~ CH 30XCH2 -C 6H5~)CH2-CH-CH 2~CH2- CH 2OH~
~C6 H 50.
From 2,4-dinitrothioanisole, neither 2,4-dinitroanisole nor
glycol- or phenyl ether could be obtained,, unexp(-ctedly. In a17
cases, only the unchanged 2,4-dinitrothio-~ 'niscle resulted, which
can be explained by the different relatioilship of cxy~en and
sulfur to the electron in the groups OCH 3 and SCH 3' In this
way, the carbon atom (in 2,4-dinitroanisole), to which the
methoxy group is bound, really becomes a positive ato7- owinlg
Card 2/3 to the electroacceptor effect of the nitro groAps. Ther-L- are

Reactions of Aromatic Nitro Compounds. V. Re-tlh,rification
of Alkyl- and Aryl Ethers of 2o4-Dinitroplinnol
1 table and 4 refc-rences, 2 of which arc- Soviet.
ASSOCIATION; Dnepropetrovskiy gosudarstvennyy universitet (Lneppropetrovsk
State University )
SUB111ITTED: July 14, 11058
Card 3/3

50), 5(4) SO-1/79-29-8-L2/8-
AUTHORS: r,'itisj S. S., Tranov-Krasovskiy, V. I.
TITLE: Reactions of the Aromatic Nitro Compounds. VI. On the Mechanism
of the Re-etherification Reaction of Ethars of 2,-'-Dinitrophenol
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol 29, Nr 8, p-- _2648-265' (USSR
ABSTRACT: In the papers available (Ref 1) it was aasumed that the re-
etherification of the alkyl ethers of 2,ij,6-trinitro- and
2,4-dinitrophenol takes place according to taechanism A. It can,
-howevxwr, also proceed according to scheme B which excludes
tabli iormation of the affiliation prod~.ict (II). in order to
investigate according to what mechanism this reaction -mould
have to take place, such model molecules must be chosen which
allow only one of the two alternatives. If mechanism A is taken
into consideration, the 3-methoxy-4,6-diriitrotol-aene would have
to yield, on re-etherification, the 3-ethoxy-4,6-dinitrotoluere,
since the methyl group causes the addition of' tHe alkoxy group
to the carbon atom of the benzene nucleus in which it is placed
(Scheme 2). Mechanism B being under consIceration, the initial
vroduct would have to separate out, oiree tlne tc
Card 1/2 the methoxy group is occupied by the methyl On re-oith-ri-

-,,-actions of the Arozmatic Nitro Comoounds. VI. Cn t*-e
-echanisri of the Re-etherification Reaction of Ethers of
f ication of (V) , "nowevc-r, compound (VII) was fori.--d which
conf irms Techa nism A - T1,e reac t i on of 1 5 -dime-u ho.-.-.y --' I bS - di -
nitrobenzene can alco tak-e place according to mEchanism, I
(Sch,nme 3). The re-etherification prodiced 1,3-di----thoxy-, di-
propoxy-, dibutoxy-, and diamoxy-4,6-dinitrobenzent.-, The
readiness of this course of reaction in all cases indicates
that the extension of the chain of the nor:zal radical of the
alkoxy group does no". hinder the reaction. A n-iw i%cthod of syn-
thesizing the alkyl ether of 4,6-dinitrore3orcinol was suggested.
The re-etherification of ethers of 2,4-dinitro-, and 2,4,6-tr.;-
nitrophenol was thus shown to proceed via the staee of fcrma-
tion of the intermediate product of the quinol ty-pe .1ecV
hanism A),
There are 1 table and 6 references, 3 of which are Soviet.
ASSOCIATION: Dnepropetrovskiy gosudars'.veni"yy universitet (7n,,zrouetrovsk
State University)
SUB111ITTED t July '4, 1958
Card 2/2

5(3)' SOV/79-29-9-39/76
AUTHORS: G. M1. Kaminskiy, A. Y~1.
TITLE: Reactions of th,~ Aromatic Jitro Compounds. 'Ill. The Absorptiin
spectra of the Products of YanOVSKiJ'S Re[WtiOn
P~~RIODICAL: Zhurnal obshchey khimii, 1999, Vol eq, Nr 9, pp 2983-2986 (U~'L;:1),
ABSTRACT: In one of the previous papers the authors showed that acetonq
adds to the polynitro compoundu in enol l'orn an-'- that the
colored final products of Yanovskiy's reaction are in frze state
only separable from indifferent solvents, its a result of the
instability of these compounds, it is extremely difficult to
inve:3tigate their structure nnd mechani-.;rn of formation thorou. - h-
ly by the usual methods. The evaluation of the absorption spectra
in the visible range yields the beat results. Thu2, A. 1,
Shatenshteyn and co-vorkers
fief 2) found that Yanovskiy's
reaction has an acid-basic character. The absorption spectra of
a number of compounds resultinK from Yanovskiy's reaction were
described by M. I. Newlands and F. Wild (Ref 3/. By means of ab-
aorption spectra the structure of the additi i products of
acetone to several polynitro compounds in alkaline medium was
Card 112 found in the present investigation. The authors synthesized all

SOV/79-29-9-39/76
Reactions of the Aromatic Nitro Compounds. VII. The Ab6orption Spectra of the
Products of Yanovskiy's Reaction
initial polynitro compounds and purified them by repeated re-
crystallization. It was shown that the color of the dinitro
compounds according to Yanovskiy's reaction is due to the forma-
tion of monocomplexes (the constants of which are given by the
table). The authors assume (Ref 1) that the reactions of m-di-
nitro-benzene and some of ita derivatives with acetone yield two
monoealts (I), (II), and one dioalt (111) in the presence of
caustic potash. The color of the trinitro compounds to due to
the formation of mono- or disalt. It is oxily in trinitro-benzene
that the triaalt plays a certain part with respect to color.
There are 4 figures, 1 table, and 4 references, 2 of which are
Soviet.
ASSOCIATION: Dnepropetrovskiy gosudarstvennyy universitet (Dnepropetrovsk
State University)
SUBMITTED: July 14, 195a
Card 212

S
PHASE I BOOK EXPIDITATION
50
:11tis, Sewn Semenwrych (Gitis, Semen Semenovich), and Volody.,7~yz
Al,?ksyr-,yev( Vl--idimir Vasillyevich ~ksey~ev_)___'
Plastychni masy ta ikh zastosuvannyEL (Plastics and neir Usf!s)
p. (Series: Tovarystvo d1ya pos"nnya polityclinyk.11 i
,Y&rayiris'koyi RSR, Se-riya 7, no. 7) 18,000 copies print,:A.
Ed.: A. S. Toplyukova; Ed.: Yu. A. Kokhno.
.F`MSE: This Ukrainia -, .booklet is intended for the Lnne ml I
C-OVERAGE: The author- liscuss in simple language the basic propcr'~-";u
plastics, th- IM"! and methods for their production, a-it
in the national e-onowv. No personalities are mentioned. 'Mer-,
references.
TAME OF COBTEITTS:
What Plastics Are
Ca=L_4z

GIT"IS, S.S.; MALIIJOVSKIY, M.S.; PROKHODA, A.M.; SRIBITAYA, V.P.
Reactions of aromatic nitro compounds. Part 8: Intorenterification
bf alkyl esters of nitro (methvlsulfonyl)phenolB. Zhul-. ob. khim.
30 no.9:3072-3074 S 160. (MLRA 13:9)
1. Dnepropetrovskiy gosudaretvennyy universitet.
(Phenols) Olitro compounds)

GITIS S.S.; GLAZ, A.I.
Reactions of aromatic ntiro compounds. Part 9: Steric hindrance
effects in nucleophilic substitution. Zhur. ob. khim. 30 no.11:
3807-3810 N'60. (HEU 13: 11)
1. Dnepropetrovskiy osudarstvennyy universitet.
(Substitution lChemistry)) (Steric hindrance)
(Nitro compounds)

, GITIS, S.S.; KAMIIISKIY, A.Ya.
Reactions of aromatic nitro compounds. Part 10: Structure of
the products of the Unovskii reaction as studied by their
abB,irption spectra. Zhur. ob. khim. 30 no-11:3810-11817 N160.
(KMA 13:11)
1. Dnapropetrovskiy gosudarstyeanyy uaiversitet.
(Nitro compounds)
..k' -

GITIS, S.S.; TERESIKEVICII, M.O.-. GARUS, L.I.; GLAZ, A.I.; SKARRE, O.K.
Reactions of aromatic nitro compounds. lart !~,: Study :-f
reesterification usinF the isotope method. Zhur.ob.khin,- 31
no.9:2902-29(.% S '(1. OURA 14:9)
(Esterification) (Nitr) compounds)

GITIS S S . FISKUNOVA, Zh.F.
Reactions of aromatic nitro compounds. Part 12: New method of
preparing alkyl ethers of 2x 4-dinitrothiophenol. Zhur.ob.khim.
31 no.10:3400-3401 0 161. (M3M 14:10)
1. Dnepropetrovskiy gosudarstvermyy univeraitet.
(Nitro compounds)

GITIS, S.S.; GRhGEROV, I.Y.; GLAZY A.I.
Reactior.g of aromatic nitro compounds. Fart 13: Isotopic method
of studSring addition products of alcoholates to trinitroanisole.
Zh,j--.ob.khim. 32 no.9:2803-2805 S 162. (MIFL4 1;:9)
1. Institut fizicheskoy khim.4i imeni D.V. Pisarzhevskogo All
UkXSSR.
(Alcoholates) (knisole)

GITISY S.S.; KAMENSKIY, A.Ya.
Relationship between color and structure in Ianovskil reactiou
products. Dokl.AN SSSR 144 no.4t785-787 je 162. (KIRA 15:5)
1. NovomoakovBkiy filial Gosudarstvennogo nauchno-isaledovatellskogo
i proyektnogo Instituta azotnoy pronyablennosti i produktov
organicheskogo winteza. Predstavlario akademikom A.N.Tersainym.
(Nitro compounds-Spectra)

GITIS, S.S.; GIAZ, A.I.
Reactions of aromatic nitro compounds. Part 15:
Re-esterification of alkyl eaters of nitronaphthols.
Zhur.ob.khim. 33 no.3:902-904 Mr 163. (MMA 16:0)
(Paphthol)
(Nitro compounds) (Esterification)

GITTS, S. S.; GLAZ, A. I.; YAGUPOLISKrY, L. M.
Reactions of aromatic nitro campoimda. Part 14~, EZ*fqct of
some electron acceptor groups on the reaction of re-esterl-
rication. Zhur. ob, khim. 33 no.lil3g..141 163.
(MIRA
1. Institut organiche8koy khimii AN UkrSSR.
(Esterification) (1,11tro compo~indB)

GITIS, S.S.; WtIlBUY, A.Xa.
Reactions of aromatic nitro, compounds. Part !6: Preparation
of the Janovsky reaction products. 2hur.ob.khim. 33 no.10:
3297-3300 0 163s (MJRA 16:1.1)

GITIS9 B.S.; GIAZ, A.I.; A.i'a.
Rbactions of aromtic nitro coripounds. Part 17: Products of ad-
dition of alcoholat-~:v to dinitmanisole. -7ht=.ob.kl-dm. 33 no.10:
3301-3303 0 163. ORMA 16 M)

GITIS, S.S.~ L'VOVICH, I.G.
Rea:,'~.~ons of aromatic nitro compounds. Part 18tMechanism of
,.cleavage of a nitro group ir. symmetrical trinitrobenzene.
Zhur. ob. khim. 34 no.?s2250-'7254 J1 164 OuRA j.7:r.)

...eac',i,-rzj arumatic nitro cc,=o~,;nds. ?arT, 19: Hffec-~ Of the
subst-4 tuents cm t,e re-etherification of aryl ethers cf 2,4-
dinitrov,henol. Zhur. ob. khi,-P.. 34 ne.10:3390-33'?2 C 1~4.
OMPA ll'::I)
1. llovomoskovskiy Lilia! Gosudarstverinogo instituta a,,,ctz1ov

KAMINSKII, A. Ya.; GITIS, S.S.
Reactions of aromptic nitro compounds. Part 211 Structure of
products of the Janovsky reaction. Zhur. ob. khim. 34 no.11:
3743-3747 N 164 (MIRA 18t1)

ALEKSANDROV, V.N.; q~_TTS, S..,S._j C~OLUBEV, G.S.-, PANKOVA, N.A.
Studying the catalytic activity of the cobalt salts of aliphatic
monobasic acids in the oxidation of p-xylens. KhIm. nrom. 41
no.5036-337 W 165. (MA 18t6)

- .GITIS, S.S.; IVANOVA, V.M.
Reactions of aromaLic nitro compounds. Part, 23: PeT-vai9rifi-
cation of benzyl ethers of 2,4-dinitrophencl. Zhur, org, khim.
', io.8:1437-1439 Ag '65. (MI-RA 18:11)
-. NovoTwakovskiy filial GoaudarstLvennrgu ins' itLit-a azol-noy
L. I
prwVshlennosti i prcduktov organicheskogz, 3inteza.

ACC N& Ap6002861 SOURCE ODDS: UR/0286/65/0001024/0018/00i9
INVENTOR: Gitis, S. S.; Alaknandrov, V. N.; Pugacheva, S. A.;Glaz, A!. L Golubev,
G. S.; Kad-Ko, L. v#
ORG: none
TITLE: Preparative method for iso- and tere-phthaloyl chlorides. Class 12, No. 176
[announced by Novomoskovskiy Branch of the State Scientific Re4earch and Desie Inst
tute of the Nitrogen Industjj and Products of Orstanic Synthsaijo (HavomoskovskLy MW
gosudarstvennogo neuchno-isoledovatellskogo I orpyektoogo inntitut szotnoy promyshlen.-
nosti i produktov organicheskogo sinteza)
SOURCE:' Byulleten' izobreteniy i tovarnykh znakov, no. 24, 196.5,1849"
TOPIC TAGS: isophthaloyl chloride, terephthaloyl chloride
ABSTRACT: An Author Certifi been issued for a preparstLve method for 1s&-
C
and tere-Uhthalo chlorides-Mirme-thod involves treatment of methyl W- or PI-6tcilu-
ate, respectively, with dry iblorine at 190-200C under UV li*bt, followed b1i t t
ment of the chloride product with water.
SUB CODE: 07/ SUBM DATE: 06Feb65/ ATD PRESStq/f-1
UDC: 547.584'582.2.07
cam

ACC NRt AP6035826 SOURCE CODE: UR/01;13/66/oOO/020/0035/0035
INVENTOR: Gitis, S. S.; Ivanova, V. M.; Nemleva, S. A.; Seina, Z. It.; Ivanov, A. V.
ORG: none
TITLE: Preparative method for pyromellitimide ~ Class 1Z , No. 187006 a
SOURCE: Izobreteniya, promyshlennyye obraztsy, tovarnyye znaki, no. 20, 1966, 35
TOPIC TAGS: pyromellitimide, pyromellitic anhydIride , urea, chemical synthesis
ABSTRACT: An Author Certificate has been issued for a method of preparing
pyromellitimide from pyromellitic anhydride. To ensure an increased yield, the
method provides for treatment of pyromellitic anhydride with urea.in a boiling
solvent (e.g., acetic acid), followed by the separation o~ the precipitate.
SUB CODE: OT/ SUBM DATE: o8oct65/ ATD PRESS: 5104
UDC: 54T.557.1' '585-07

ACC NRI-A?6029051 HCE CODE: U 0060
(A -WOU3166100010WOO6671
lNVENTURS: Kudryayev-tsev, G. I.; Tokarev, A. V.; Gitis, lvanova, V. M.;
Seina, Z. N.; Lyubova, T. A.; Nemleva, S. A.
ORG: none
TITL6: A method for obtaining modified polyo thylenot crop lAh ala to. Gla:3-9 39,
No. 183936 fAnnounced by All-Union Scientific Research Institute of Synthetic Fibers
(Vsosoyuznyy nauciino-isslodovateliskiy institut isk-usstvennogo volokna
17
SOURCE: Izabret prom obraz tov zu, no. 14., 1966, 80
TOPIC PAGS, _-,"mrPA4 polyeUhylono ) Chemical 'sylltha.-Ao
ABSTRACT: This Author Certificate presents a mothod Ct-ir nllti.ming n modified
Polyet'llyleno tereplathalate hy introducing iTiodif-ring in the course of its 1
To in(;rC.W30 tll-:) IlPflt 1'0!~i-stancn of Win po1ylimr mid nf ts products,
I.,JI-mrtional ()-r -')yrorlnl.lVJ-,0rlQ (for P,N
ro;vill.lil~iviide or is usoft ni tAir~
51JB CODE: l1/ W-Prl DATE: 01jul65
--j I h I IIV' -Z-70 4111. ~-l

YINOMOVA. H.D.,rabotaik pavil'ona,; GA INA, A.G.,rabotaik PaTil'ona,;
-4GITIS. Tajo., rabotnik pavillons.; MGACH"A, T.I..rabotnik pavil'ona ;
ZAK. R.G., rabotnik pavillona,; RAXSELA, N.A.,rabotnik pavillona,;
BAUT, YO.A., rabotnik pavilions,; TAHAWOY, G.U., rabotnik pavil'ona.;
TOKASHUK. F.A.,otv. red.; DMITRIYEVA, L.A., red.; LUXIHA, L Ye..
tekhn. red.
Lfar Bast] Dsl'nii Vostok. Moskva, Izd-vo "Sovetaksia H40fia,"
1958. 109 p. (MIRA 11:12)
(Soviet Pal &at--Agriculture)

1. SPASQKUK-0TSl.'=, 7-T.0., Prof.i GTM:, YE.I.
~ I" M
4. Connective Tiosues
-viral of "On:~,c"ive
Fwricti~jr)al :itate of phjsloloi in 'r!':
'ru. 0. 31 -lookutit's lk-vv; Yle". 11 '-.1
T T
9. Monthl List of Russian Accessions, Library of Congress, Uncl.

SPASOKUKOTSKIY. Tuk.; GITIS. Ye.l.
-
Indexes of the reactivity of the organism in animls of dirforent age
groups and changes during transfusions of isogenous blood. Fiziol..
shur. (Ukr.] 2 no.1:58-66 Ja-IF 156. WRA 10:1)
1. Kilvalkiy institut perelivannya krovi i novidkladnoi khtrurgii,
viddil patofiziologit.
(BLOOD--TRANSYUSION) (AGE)

,GTTIS Ye. T.: Atater IMed Sci (disa) -- "Tile effectu of' trary3fftiol-rr, ~.sof- nous
blood rind BF-P. r)mtrjln blood aubf3I-,IIIUt,,- on ',j;f, Nnc,.Lc~ml- of the cerebi~jl
I ation)". Ki,-v, 12 np (pc r - TTS
corbex (Experizm~ntal Lnveali(-, P 'I s , 1SI., infit
-mnvPm!cn iffi Fn-rF-~,nr,-,
of HIMIor Nervolm Actlvl.ty, Kiev Sri Bgf-. net of* I
surgger7), 1~)O Con,es (n, !.10 1, 1--)

GITIS, Ye.I.
Effect of transfusing blood and protein plnamn suhgtit-ito BK-8 on tLe
higher nervous activity in white rats [with sumnnry in English].
Zhurays.nerv.deint. 8 no.31418-430 MY-Te '58 (MIRA 11:8)
1. LaborRtorivn pAtofiziologii Kiyevalcogo Inst"tutn Derelivanlys,
krovi.
(C'MML NERVOUS SYST3M. DhyalolopZ,
higher nerv, acti7ity. eff. of blood trnnsfusion A
protein hydrolyante BK-8 in rnts (.Ru3))
('31M TRANSFUSION, effects,
on hipjier nerv. activity in rnta (Rus))
(AMINO ACID MITMW3S, effects,
protein hydrolysx;,.e BK-8. on hip~her nerv..Activity
in rats (Rua))

SPASOKUKOTSKIYP Yu.A.; CHERNOGOROVA, Z.L.j GRINCHENKO, A.14.1 YELIYASHKEVICE,
B.S.; G~~~Ij SHMUSHKO, R.Ya.; SARNITSKIY, L.P.
Effoot of the BK-8 protein blood substitute on the process of blood
coagulation in dogs during a stomach resection. Trudy Kiev. nauch.-ioal.
inst, perel. krovi i, neotlosho khir. 3t120-128 161. (MIRA 17:10)

-!nl n
ir;it it,

GITKIN, S.
Order of the fiXiM9 Of Pensions for meritorious service for
medical and pharmaceutical personnel employed In medical
establishments and durgetores. Zdrav.Belor. 6 no.2:79 Y 16o.
(xmA 13:6)
1. Zamestitell nachallaika Flanoro-f1riansurogo upravienlya
Min2drava BSSR.
(XVICAL PIMSONNRL--PSNSIONS)

GITKIN, S.
legal consultation. Zdrav. Belor. 6 no.4%72 Ap 160. (JURA 14-5)
1. Zamestitel' nachallr-ika Planovo-finamovogo Upravleniya bWAzdraja
BSSR. (MLOYFXS, D13KIBSkL OF)

GITKIN, S.
Iagal consultation. Zdrav. Bel. 6 no.12t68 D 160. (MIRA :14:1)
1. Zamestitell naohallnika Planov4-finansovogo upmvleaiyn.
MinisteraW zfravookhrananiya BSSR.
. (MEDICLL PUSONM)

GITKIN, S.
Legal conBultation. Zdrav. Bel. 7 ao.3.-79 Mr 161. (MIRA .14:3)
1. Zamestitell nachallnika Planovo-finansovogo upravleniya Min2drava
BSSR.
(MEDICAL PMONNEL)

SKLYUT, I.; GITKINA, L.
Second United Conference of Young Neurosurgeons. Zdrav.Belor. 5
no.12:64-65 D 159. (MIRA 13:4)
(NERVOUS SYSTEM-SURGERY)

.-- UTKIA,_ L.S.; POLISSUTA, L.P.
Recurrent paralysis with involvement principally of the ocu-
lomotor area. Zdrav.Belor- 3 no.10:27-29 0 157. (MIRA 13:6)
1. Belorueskiy nauchno-iseledovatellskly inatitut nevrologii,
neyrokhirurgii i fizioterspii (direktor - Te.F. ralitovskiy,
nauchnyy rukovoditell - professor B.A. Markov).
(BY-1-DISIPASES AND EMCTS)

EXCE IPTA MMICA Sec.8 V01.3-1/5 Vouro-PaychiatAw 58
6. Y.' 4(1NFAN/TILE)
437 /E