SCIENTIFIC ABSTRACT GLUZMAN, L.P. - GLYADELOVA, V.G.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000615510003-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 19, 2001
• Sequence Number: 3
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

KRUPSIIT, B.I.; GLUZXILN,. L.
Using electric "W spraying In tho repair of . soul-Outting
machines. StanA Instr. 27 vie.10:32-33 0 456. (KW 9:12)
(Metal spraying) Obehine tools- Ropatrixg)

M.A., inzhener-fisik
)bthod for determining the radioactivity of aerosols In the air
by the aspiration method. Ng.1 man. 25 00.2979-83 P 16o.
(NTU 13W
1. Is sonalluoy radlologlahemkoy laboratorit Odommkoy oblastsoy
sanitarno-epidentologicheskoy stantell.
(A32--AYALYSIS)
(RADIOACTIVITY--MSURIMT)

BEYGFLI, Z., nauchnyy sotrudnik; TALIESNIK, Ye., mtuohnyy sotr?idnik;
DUSHNOV, Yu., nauchnyy sotrudnlki PARY.HGMVS?,ATA, Tj., nauchny-
sotrudnik; GLUZMAN, M.,,_nauchnyy aotrudnik
Effectiveness of manufacturing highly prefaVricated reinforced
concrete elements and joiner's articles. Zhil. stroi. no.b
5-7 164. (KIRA 18:11)
1. Nauchno-issledovatellskly Institut zbelezobetonnykh izdeliy
stroltellnykh I nerudnykh materialov Glavnogo upravleniy&
promyshlennosti stroiteltnykh materialov I stroitel nykh
detaley.

16.;i:;;;:;: .1 V 11 - -
14
Sir
8-
f I
ee.t I 600mus MWAIL
IF. AL Two=
99 1311;~ "d a,
I
ubdlw
aua. pramem W. I
.%01 Ct AIIWKAFO"
-z7T
V919,10 It QW.
I- T
0 AT 00 01.
11 1" ,b 1, .11 11 1~1 I I., "1 1.0 1: IW

MAPS
4141v.
h
i
Iwo. ss*
coo
pri
K, a 0 0
Nee
be*
0 ol I I, (w ort-
a .0 w a s As .3 3 4

~lvl Ir.ill; WOM MOV! N 11411
q a 11 a J, Its StAllop wpm 41-0.46to
A -A JL_k_j_jL_I~ OR
Is AIM A_ll
4*p r'3A
eA
fit
-offs
Ito. I.
00
go
...... ..... ...... -Of
O.P
00
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a Coademution perfiducts of N-sturrimitcArksuolif (biplitim;4-
coolirdrazine) uft flumfoorlo &SJ Its defillstivilill- XLKII-
00 a I*rujl A.A.40%.t.. rlm,4111. I'mit,
of No-jra. /Av. , No, 4. MOWN11-Con-
-00
041 .40 im-ticA1,41 by Wwlsu,l (C. A - T. W rd by I
eqj C. A. It. 4.101) Ily comIrmin
It I with at
0411, G obtainiml flilfifflictlic 1111,hrOY 'WhYd1`1111,111W, see
NN
0 t-datsimItIt t"Ovitykitrity4ramIew fV) by mww",ation gee
w-th 2-rittisaltuternurse (III). Tfw uwtbW &w the
-mit, tsee
"pts. .1 N --athat,,le and III I was itutsiretvd. I'm Ir gee
eel thr pfelm. 4 IV hesil Im 2 A min. I S. d 1 fast I S. 11111
IV r~. J k-, with a dt'll' Of ntfk~ FINW.. I.IIIIII-MI
'00 'r
Ulkt 4,, d2ftkrA MUM OblAillrd, as 1 31 (rupki best. see
:
.1 k. lbe Im-pil. 4 V livAl 1." 3 .11111, 11.5 K; of 1 and
412 44 111 1" IM vc. III &k. with 3-4 thups of HSO,.
h,, 4. iws j; -) ftwmed ml nettlics from sic. The m. p.
w&. nt -hArp. A chanim t--A p1mv M 177* and twitissit
at Tlw,.%)Iy. of IV and tA V are givm i" a tabbr. goo
W~ R. titan
bee
Ito*
woo
it
..........
5;;-v -a., wee
is As
0 At 7j'
%IWO
0 0 0 0 49 00
'a , 00*0000004000
40 ~00 0 0 io - 0 a q 0 0 0 0 0 0 0 a * : *0

Is b Is 4. 1.
AA K W 11 1 .1
A,

A 41 Amino dollystivIIII 01 Ufboasolo and fiLwooodo M. fidlur'l 11110 It led I.. LL,6 W. jamrM MY" '41

1*
rh. Xkiw. K4.Wkov. C"...d4r,
Zh
8
)
Kki
R
I
N
7
4
1%.1
*
'
t".
f
r"ll.
up.
o,
-
S. ILI Vill 11"4
,
): fkl'
;,:
00 ic with (AK obtaWilia The ItIM-1i'la" wvtn
Aftickrolve. ket,scief and a- 41"1 *rrr Rtllflk*d'
t 'a
st ow wit It Ilh
Co
Mich1
r
ti t4rTIC41 klitt III 14b' , CkI'VjW1 tilt List 11146-6pil. "lli%'11 Ism
e
at
v
,
he A Ilt 11sat ItI41% *tit
, .-,jjrkI ."it Ill t6- A,I-ho. -4 1 4-1l, %4 11,IZAN in-
tw"I(XIIIIIIone. tobs. 11 tjW YoLI41, &"IW tit tile haphit"Irkne-

(Itliltme. a-IMPM11%)IIII(Wele. s III III " Ilk 11. 141111 WI-M JIN-411111lit
naph1henefluilltifir AM O."aWlIbIwItliINVIC. Unfarst'Allic j.'I" the I'llik.11 111 0- 04 w4lef [his
wege cAllejuni in "%tvdr'v4t6snA wilh kril"ll's tilt ONO prsiml% III,, -istro Sold I"Ifit"alool a the twt-MVI j -0 0
with altichydet 4lul veiluttor- vid-1-1 the eAv.
0 4D h.H.Mills .,h M".h 'V'J'

00
"Ce",
henzahlehr-jr. its. IM-4'.XICVf--TrM'W cirytials. 11)
' Ill Alk, with themuldn
kin, 111. (31 ph"vointwet"ttintsm. "I. =I-7 Il ttIlly the -.IfAtt ')I Was t*,-
(dvconlpn.). ysepi AS-70479; (4) ac"uphthenequino": i4itim. rrealt.wnt 01 4k. Will. I)( 9~jIjIXrjjfII4jjW 11,11h
Wucjpv= ctrystah, no grhWift the crotak arv tMI14 A.1)JI -0. tit aussiuallowtomw KAWV the felt In-slu)- %~
I
ofrtiv,. tit. "J; N'. .4 ju&I A ytik-- n.-I
'So
olcttrwl.. in~ IN th, ila,o4k. A. and the do-Ar kfis.
I'nollittic list, y0h)w ial-tatstv with C110,ur brissenef4vt "
41'; .00

4r
l the yviWor-crell tli-.%c kriv" fn. !W1111tv
Ltnngkis. id the fitono- untl di-Ac dcri". with IICI M's.1
IkAl of
I IV*
will tie IlIghly U11 Ilse
-
quint"i" fit rt
jet at tiniv I d tile ead.stivi 4r, I" - .4.
m
IdAttir-I frinti The 1hoolif 44 lytro
.
-tr
f th
ci
s
i

Ji gi 4
v
e
it
.Wjniuur
ti
o
ft
throlf.y. W It. Ifenn

too

'o; Woo

u It U 99 st 0 Nit INNO 4 I'llf
44 4 4 VA
,
n
a
*
;

0 0 0 Ole 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 0 a 0 0 0 0 0 0 0 a

I I wig q a I 1
nI

I
if q off 11 it 0 0
4
J# It a If III it Id a K v a A 4 a a it
~6 L -1 4e P M
A
it Llj A...t. A-4 11111 A I I it A. All A
.
."

milkammimmi haami6spill

viliodst"r tip -4111111,k At I J~
yield Ity nitt.matitm is( eArtiatille 411-1 ir.
dortion,4111f, 1w.-twt fly Zn,fta,l 01 1-1,411--fief If. 11~~
111410 rIt,

ill. IIrj q. of lillw%, Wit
oil, 'T.) fit
(Iftmil EMIJ); 1.."
lidl
M' (dww1
ou
Katiju
M
k;
.
.
.
p
l

AA

Its

,
:0
Z v 0968 4

010199999
.
.
0 0 0 0 41 0 V 0 0 Ill
_
9909 0 0 0 0000 00 F 0009 0 0 0 40 0 0 41 a 0 0 * 0 0 0 0 0 0 0
0 0 0 0 0 0 0 0 0 0 0-0 0 0 0-41111-04 0 *_4 0 0 a 6 6 0 0 0 0 0 0 0 0 0
4 to
,
goo
-00
.60
z r
see

Ole
t90111106400008090
Is 1: li W is
C, S-.L.-t
0 4
so A
06
go,
00
00
00
00
00
00,
't"10 0 0 * 0 0 9 0 0 0 0 41 0 OV,
U At 16 AT a w If A 0 .1. a Q 41 4
k.A

Proclucts of Scoylatlan of I-amincifluarmitar, V
,
1;
k I-so
Kh. (311111tan. C
, ~. 0
.
-Amyl4two
son-it (1) by czem Ac.0 yiel,14 a 1: 1 triol. cimniml. -4
an.1 AcCl gives 4,tslv the monpi.
Ac SWY. The mol. cionijkl.. forTiml in SWW" yiMs.
Iw-193-i" (frutts Etoll); it is rewl 1. into it. (!,Ml .
= rosow. The tiNt
,one"re b
tritat"Will with CHO ! -go
I.
1
y
movii-Ac C.Wntkl, 10 11.1AI IM 1.41. W bY t.101,14A 1.1111 1*0
trafene 2 -3 horc. The mmut-Ae -feriv., its. Z.N7 -X". toing
ittwol.. Anil the di-Ac4letriv., III. i,m r iff,"t, Fmtio,
bring rtrovvir"I fromn rise wilts. Jlo)fh loriji rv,t. /mflf Soo
mUstrit and rewlily by-Irtillitable 110 jaPt whwh Are heu A-too
tworpl. by PaWns dirr 110 into FtOll Toe 1. nzow s4n%.
of the controls. Use of excicss Ar6 in the 4utylatimi of 400
1 vickk the itiono-A,-.1criv.. in. 2!~i Wift.mot Violl'
zoo
M
too
JS i
6 1 L A *IT A GKAL k,tCR-%Wt CL ASIAPIC a? tf a
7;:;
t I , ,,
-jr-_ L. T-j-_f . j~ ~-P'
, 11-
$0 It It It ~4 It N a 4 9 n of a it at to 1
0 0 0 O.i 0 0 0 9 SO 0 0 0 0 0 0 00 460 of! 0
0*0000010000000000000*~99.
11 __ A~o
.00
2see
'00
zoo
40
000
000
w S IT IN 9 a
00 0 0 0 0 0 00 o 0 000400,
O-OLO-0 0 0 o 0 0 0 0 0 0 0 0 o1
i

P
tonaitillymmkrkic chemoo, In 1-methosev 7 stploolisidu At "maises
st , 1, tillian'.41. 1. *4 1,41411.111. Owt It I I ImLm.
jkhAok,-W!q;iIc 1.11W). ZA.t. pig lik,oll, IS. 10 lzi lot -1,
- AmIrlatticlil ill J tI-4L,,oI
MIMI "Ilsorflorr. C.A. 12, lusip) Nism yo,1140m, 11) hit lilt 1110
ing at All 211)", 1 sivirs It. In. 2.37". 01111111 11~ 1.5 loom
Njimlormil 11114 Plicl stplij. W 11 Itikko 1; lart .... lilt& ,( Ill,
"tilt whl.. llivvw It Not wo .1midific Ill I M, Iff"llat mij#f.,
the ml ervolmis 1xi-mosp villipw 21try I -~' Jim Rivoil,itit, oil
It frimis A%Olil imilit. Kivei 1. 1 he till-I. it is. W I 1411d 11 tile
Identical. 111.4h 1,411.111 tile matiletts., ..I Ac stomps
No wrialit cluillite to (.1iwfvr,t t1lill"If Or I 011.11M.11 S.. Cl
4. dell,t14,41 Its I fictrO.I. III'm 1,110 ri.,b- .4 1 .00.1 11
II,s%r flir 44111rwhn at Ilor ,Ii,r Vill- -All Awl
Int Ml knim.A. k'1114. 11,1111 Ill'.1 II"-*t M tilt 11"We 1.14-111I.A
.ImAl.ti'm its Ilw .-I Wit aji,t,
diftert,"I I f~,v AD, 10

GLUMN, M. KH;DASHMSKAYA, B. I;YAVLIIISKIY, M. D.
Preparation of pyrimidine from mother liquor. Mod. promyshl.
SSSR no.2:29-34 Mar-Apr 1952, (CLML 22:2)
1. Kharlkov Scientiftc-Research Pharnscautic Chemistry In-
stitute.

!P fig t~H' V
6A 2- 1-f
i r
si"
lat"iWarga - adf 01111110mil- oil 01 -0- 11
It Py 'tbsiltoli
i" 'ID-9t,
6tie. simid 4A4-
L M. Utvidett (Khy-kw Rgg T m k to t 171 - 0 P1111 it"
La); X (11 y I~IUCO' 1 0: i Intif 61
u" ' , irm, M~ gzs-~ I
KLw"1m. 4'" Sul p
(1) a MA 0., Mt -oir: SQ:5
X. (url. cjf.),S~ hei-ted I mr. Em 2.1 1 ,l'. (J1 0ftitta Nall ~k
mi. atm. AfrOff and I I GIV ACOR ravt &R4 147 to(*, 11144% yd 1, 64441111. ( It, Em)-lils"CII-I't 0
)~ V t1l OT 0" ~ 1, 1 Ilse
which. rubb,,l with dry MegCO, W&d OL~ M-N-1 1-1
0A rfil
C11(CJFlOlAC1TrP1i-SG, d
ridine). Tfils (U.4 g.) xaA 0.13 C. N&AL-I'd a
M. tivillmill. wil INI'. 19-Itc-
In 1.2 mi. 140 And 2 nil. R(Oll, C*4.4' dem-ited 11wvqrt Cd dry Njr4 't PI/7 111111(m:'M 0101311 t
Isom it gawfl ppt., and heated wltb HLOIC-Etio in I ill, F:Q". Mr.01111 NIK4 t4i I lid thsj~- lixi di-i k
Civic 670,10 amomhous blsutfite "alplet, CarnOWM&A'do, arul Jiln. withdry'r .9 It t
205" -37X. (079 P-ridlac). ~.Wuv Uq- ~ff siff "''CrAL ill I[ t
4th ON-adda.-W
WCfim(LW;OffNCffC1fjI*MIj, deccan . 180 -10 4
P, 49~ M14 !44*4 d" PO tio, U qrv". t 401i Itt
-16.9' (priillm). This mdam Feliling solts., 4.104*0% WIC IK4d ~Plb WM limitim Mi E.,
I Y el I
fairly slowly, and reacts &lowI7 with ammorsi2caj Almos. ,l,, tmil
'Sinflar mupliz& of I Tssolt I with "xma (2.45 If 11 Ittle AcOllf I it rattdt',s the its
~Xl ti
C~gr
t%NCj1.SX)jMff4Nff* gave &5% p-GY witill
fing.
IM, UTOM a Inta till
deconlis,
I Cori! in: g. A ligth. . P
M40 , (*I'D* -29.6 (pyrklic'e). With lgcm V.- of the
", "Y" 104"' il
UfC 14 E-f
Acoll cnncn. Its the condemation to Cy 00 "nctiall id
yields a new rutrtimee; thus 0.4 r.711nd I g. andetankro- iri Ottliomi C n mimts,. da
diphenyt sulfcne boiled in 3 ml. mbq. meoff itsul 0.11 C'
AcGIT I bLr. rave 84% SOj(CF1'(Cf1OMX11. "VilWASm-
tMine), w ich hiled to yield a isIVAtflid tk*nVlV%. RbdUC-
tion of 11 In aq. ak. HHGH with H13 at soon, timp. gist
4

OIAIZWI, IIAM..; LITBlNXIIKO. L.M., TUKAIIEVit, Yq.
Syntheuis of derivatives of dic.-hinovooylaulfone and sulfoxide. Part 4.
ties is.of 1,1 0- fone und nulfoxide. Mr.kMa.zhur.
Synt iminodichinovosyloul.L 1.
18 no.2:11)4--196 151"P (XtRA 6;9)
1.
1. Ilharlkovskiy p.-osudaretveWy universitat.
(Sulfones) (SmIfoxides)

.1tyl '141folto Kim
of dotiviltives of cliquinovoryl fitill'one nrid rdf. W,Lll P-414d.17 -Nirrivilt, . ji% c( rv atil
. 4 w1 ItS,.Sj. lom,ler,
log N Ycf1$* d. Crt
M. KII. Ohlo!vul .111.1 1'. Ill. l'iftimilko (~115tc Viliv.. (mrimWm n-11 thn sk-lo'bl- dots 1%01 litix,1111 to
M to L . With AN RAt of d
Alk 151:12); 1. CA
tmlj~yllriia lit ~11.
48. lUlld. stilfolic (2.2 g.) l1criti, PhN4 or tet i
%vith rhal,iltgaild conlitir. V; 22 nd. lifir In AcOlt Vill! = .1n, J-101.glucoddeq of dlqu '111.1ulftnill.. X1,
(o. IN) o%cr 1.5 ho.. an(f the 5ohi. %%a:. kelit at foons tenit), 3 of diclultlovUNI form (1) lial't Ili-
MR, then ticated 'will, coullog %xilh 100 tilt, Ice-IhO und
filictut Immolimcly. the th.rnqighl,~ vvd~hct 1411(1 drie yc!lc Strut:tUre. estwittitilly Lh-31CHAW NIO Ac Q It ir.
~(4, ( I
Ilk. The condinsatioll protlucill of ON 11
liminodiplienyl sullone (11) or the flitral Villio Littill'i: (111)
pr(A U c I. Ot:l i lit (I in 05% Yield, lut% O,S jcjrcjf.~ C110.11 Os
___ -1 6
(from %tOll I62*(CIfCt, Thin JO.3 tl.);And 0.3 g.
tit 3 ml.- C,lt,C , %ere re.flu
J,ced 60
Iticating has to be. stor-.vd ivH&HI Tarketil beTirls)
inin. I 1 26 M dr
cool-d capidly, and treated w th 6 ifil; Y 40 a.
tr, dlicr; lilt: VLWous ppt. yvasAashed Aith more dry
N
0, virlding 66% cvrrespondiiig N-fNcoside, C.1faO~,%-.-
%vdcr, falij 1,513* (1
iyrWin~).. similarly ocid"dyl-
d'
SjFcjh~vosyl suffaxide icau the aceladibranio drriv.. CsHnOja~
ri; -
Jxlwder. (froin 13t. A~); JoiN 239* (C~JICW, which.
have, tilt stilletura of OrAlmilthille t4w 1
P) -$1, Of- WIN '111* 10
lit
C1I:NCGHdltSO3,# ~t_he guicaphle Irti it 1 310 iti 11" 1,
_40 1 hexa 1i fera..
In Pyrld,"d with e30 $k,) S.1
8.2.
decomp. 172-4*, jal
L, lubsta n"s is mid ly dcnit~ It), irnt
groups in this sniti Win
Ment of the sub.-ttance fn pure Mw4CO Ill it 0,0 lil KI;)H It'
AfeOH; the deticetylated glucoildt. pptj61 11diniedlatelit' the
excess isticall, is back-titrated. Ilia conl 1, l;;4,i of
I 7vith 2 moles 117 Irvittit with AW-pyrfi is( loom
I
1r
tem d*t4r., CjgtIl
loft

-GLUZUaJl Lt. KH.
ee).I, l7a-4,, -kii*l' i,m-v. :ns,; r,
ClIsCHMet, 151.8, 213-20', 20!`~.10' ' X] 'I" I
llV1flC11(CO4Na)C1fj1:74CW1. 45A, 1&0.,3", _(Lbi',
.10". 20.50, 1, p. 110 Clfj ('111 Of(KIII) 001111 70.71

89, 45-70', -17.3", dvciimr. 1.W", 09.1-; 1, Jvacm.
CONIrCHIC01111 3111. 1115--o , -11.5% - - Ill HIM.
C11,O)IIII, W.2, IW*, -8.2", 1 W-M-, 281'; 11, 11,NCIf-
fill, -23610.
112NCII(Cosll)CFItCtllg?V~3-ijidL4j,-I
-24.3 *,-, -; It, I N11,
"
411.6'. 05-100 M.S
; It, AFINUIXOMIC111cwt!"
4
*
t
0
W-30
, -10,9
, 1. N IfiCTMOAU, W, 371-5
.
73, I
-7
-Ave tho sarne
dircil
sed with Dik(Ollh
8% which h
.
y
y
g
product as obtained from Basalt of glycinL above i lil[Oll-
24sopsopylidene) (R -I quinn-
FII (111) di(1
CII(NHR)CO
,
I
0"
40
1338
72
i
ld
5% 111
1
-
, . -
e
.
lirm-0-yi)(
) in.
% y
.
'
.
-i
1
1
l
h I
J
i
7
U
f 3
k
f
U11
4
nin
ii o
ucoic w
t
P?I(
.
se o
tog
t a
a 1
.5
11
4
ioprei.
Ba salt of tryptophanegave the 114eiiii., who%c di(1,2
P lid Aw) d ' 28't"
(K)AM"
The I ditriv
w
its

.
.
.
,
,
NH
C11i dirrisil
U

I-Sugar derivatives of amino Vida. Af. Xh. Glitzmais anif
'
l
il-
W-
-17
'kit S
V
1
K
t
k
A
H
G
X
OR ,
I
(11%olin. Z32j'- ITIV; the I deriv- of N111CA , tF1
'
1
11
.
ov4
en
.
.
.
or
t
e
11
di
.
b
o (
,
'
l 11
rit.135-
QV) Ol-isapropylidewe drr~v.. 1
1ji, still a -3.4% W.

1,A S.S.S.R
*ad - 87. 63AI952): cf.
Ilep-
= 41)", the It (It-Av. of 1j,A*(:7AQA11)C11*CS"tO/1-jb
itj.
d hI g. C-4. 32. S3700.-Supr derivs. of amino I,24YvPrbp~id4rne drrii,., $3%. Its. 100-400, a -3,2". The
scids are readily obtained by beating sa equirlsolar mlit: III Wallorst of th- residur, iin tLe 11
Bst salt of an amino acid with unhydroglucose on a StERIA histOilrocitfi-riv. wanirsailt: by 1.4lulctischliger Ilftatim CC.A.
both 21-4-hirs., followed by removal of Be with 0.44Y H.-SO;1, 1AJ4d0),-*fileh shonctl*Ojan ths- noclear N wa% iiiisfimtol
evalin. s .x tucup, fomtatio of benzylidene deriv. and purill-
Mn WhilY'Alli Nift groop irrilctArl willi -_1 owles of
cation of the latter. The procedure can be applied to dh
051ii'll
t 0
(01-1)
t b
i
tid
b
d f
f
d t Simle Taild: Ware, 11117,tthlo ill air the cl--avare off i%oprlripyt-
'Th
. i
5114' AdOL
14
I
;
It
1
Al
l
.
a
orma.
r
es,
u
: mus
e use
or
an
pep
h
id
l
i
i
h
i
h
d
i
l
W
f
l .
ll
11
e
re
U
.4 Ivas 111a1
t
atm.
l
fulle
i
C
K
M
n
on of
as. o
t
e plept
es to m
ze t
e
r
ro
c
m
l
yt
y .
.
'.
ll liki. limb3bly Ill pyl.1111+1 11:1fir,
w
e I I,,, X-tsion"Wit4wr-6-yi (1) and
rat" Th ole"
c' g
4
i"c' the deriv.

P
4 '
C ll~

I.. add
d, rill of t h e 12 -
i
?
4
d
ii
de
I
~
i
;
!
i
1
erl.: ) (for
n d
i
-tirril
y
~
.g. .I
. aruI and .4 A Ovelill . Nil. r,14(y)d

GLUZW, H.Kh.; LITBDIMO, L.N.
Synthesis of deriTatives of dichinOTO$YlSUlfOn6 and sulfoxide. ALTt 6.
Structure of If -glucom Ides of diahinovosylsulfous. Ukr.khimshur. 18 Do-3:
320-326 152. (XL" 6:9)
1. lhw lkovskiy gosudarstTenuyy univorsitet. (SUfoneo) (Glucomides)

GLU2NAN. IV. Xh, and 1"MiLETTKO, V. 1.
Sugar Derivatives of Amino Acids. V. Interaction of Anhydrog-lucoBe with
Pheryldiencolic Acid and Thiazolidine Carboxylic Acid, ruige 462, Sbornik
9tatey no obshchey khimii (Collection of Papers on General. Charistry),
Vol I, Moscour-leningrad, 1953, nages 762-766.
Khar1kov State U

ax., ab, v q
2 6'_ SY
do,'ilvaIdees a' M"U
I dad ti"O. hf. Kb. G k
!Ciorlkil State Wv.. Kharkov). Zhup. Obikkel
AZ2-3, "(1953).-A review of carbohy4rate-protein
atid carbohydrsite-peptide complexes in given (3) refereacts).
Prepa. of amino acid complexes with clarbabydrates 13 tend. 4
By accon plished by condensatim of monoseetweenhydro.
glucose (1) with Da salts of amino acids, which mutts in the
joining of C-6 atom of the monose to the N atom of the
smitioncid. To soln. of 67.8 mt. 0.2N Ba(OH)3 land 1.1 g.
glychle was added 2.78 S. 1. heated on %team but 2.5h:s..-
ift rtmOvtd With 11150jo the filtrutc arapd. in nicN4, dfird
at 9(),400'. boiled with dry EtOAc, then with MftCO and
Altered; the solid was washed with hletCO and 18ttO leaving
behind 85% ],Visoprop idmequindros.W-6-N-CiXive. in.
1734". [*IV -6-3* UIX; Its aq. win. I% seld. dit"4ves
B&COs and such soins. ppt. Ba only with 11,110. not with
CO,. The product is sol. In 11,0 and ArOll, less in 707,
EtOll; Al sail Is a white solid. The product $ydrolywd 3
hrs. in H atm. In 50 ml. 50% AcOH. rvapd.,,,Ond dried-
F*N-11wisit, in. IV V-81
ve " "91 1i9.. Similar re4etloll of 0.10
lycitse In 24 mt. UN 13*(Oll)t will$ 2.1 C I JAVC iiilk
tn. 168-91.
to] V -8.2'. Ills doe% not r wee Vehling st". Hydtoty-
sit with 50% AcOH U above followed by tilo, of the litod-
act with hot MeOH gave some W%
Cl.wine. decomp. 110-20'. [alit 23.RA
(H.0), Which re("
warm Feliling soln.. tmt givri no mlor with oinhydtla.-
Heating IM 1. 1 in III MI. 411). (CHICIh with 1.0 R. FIIN-
CII'CO~Bu to W70' followed by 3 days at 1"M temp.,
concit. in Poems. heating the residue 3 lits. with HsO. exxti.
of the residue with CHCh and evapn. of the itxt. gave P;-
Bu titter, an amor-
phous solid, softening at 50-60'. [alit 14.60 (CHC4).
TU condensation can be run by heating on a water ba
(V in (CIIXI)t-MeOll. Hydrolysis of the Ru tamer 4 its,
4 it*,
it room temp. In 02N DA(011)1 gave 247, N.(1,24"propyl
Idene4l-Aul"Ovosyllillycine, in.. 113-AP, F.4
timl ~itl_the above preAn. G.

GLUZAN'. 14. Mi. ; ROVALE,'4,'KO, V. 1.
Tyrosine
Sugar derivations of amino acids. Part 3. Condensation of anhydroglucose with
tyrosine. Zhur. ob. khim. 23, No. 2, 1953.
M*nthly List of Russian Accessions. Library of Congress, June 1953. Unclassified.

GLUz-1,1AN, ". K',1. and XO%,'IJ ENNC, V. T.
Sugar Derivatives of Amino Acids. VII. (,uinovosyl-n-Ardnobewoic Acid and it'n Derivatives,,
page 469, Sbornik statey po obchchey khimii (Collection of Paners on General Chemistry)$
Vol. T, Moscow-Leningrad, 1953, pages 762-766.
MarIkov State U

GLUZMAN, V. a. and KOVALMEO, V. I.
Sugar Dez-ivatLves of Amir;o Acids. IX. 11-Glucosidei of Qutnovosyl kil:;o Acids
and Ar-ino Alcohols, T-~age 476, Sbornik statey po obahchey khimi'L (Collection of
Pa-7,rs on General Chemistry), Vol 1, Mosoew-laningrad, 1953, I-eges 762-766.
Kharlkov State U, Inst Chemistry

11 S S R
7W C- 41 4'
.'. . I
let
14-

G L U Z:A
A method of determining the temperature 0 applaraner
>'rrrU a ditture Lof Iloild rMug t".
G (11 IS. ati'l *.I, I "rillaiij,
--riMI"Ote Umv., RI alkov), ellar.
26, 122j-TUvTT)-.--Apr =irrit'ice of a fiqnid r4ia-ls, juch I.%
a eutectic mixt., call fit! ob.-wrved mi,-,rowopicidly fly tile
rippearance of "Contact Inciting- pf a !111,111 piwe of efit.
sulid phan oil a thin laycr of the oil a tuitabli, nicitinji
V. N.,
"Ilk

'Ifulpencl in w.11-0flulliblium III systniq of tho malry-
~
n
enhwur, I.,
dildet iinhie tlpe. M.
11 W.Agwain, A. L.
S l1q4t.6k, Ip. .4. YIPAOr IA. U.
-
'
'
l I
~
Aup KhIll .27"
,or
Ny Sulu Vn
v.. Kharknv). ~.
ZO.K3,: cf. C. 4 43, 7110j. ~ 17111 vt)oCIr1Atx1; Ot A
qyii4 slim C.1-11)llt tit. telli
Esr 111 1). (4) fl: tfi~ tntectiv. (4 +
(C.t 1! C1. w~wrr v lItt r A or.& is an ita-ioit, th-t ntivir !it ailt
(or oclif Ile ichl clilorld-), sial C !4 the
wMIA. fortned !u the r.-actiou of A ond s4, %its nburvell -
bv Ole "imp-Aw convrd" wAhod: N Olt a crysisf of A
wa-t plict-d 0 1 M th in IAYC.- iA 11 at sevM1 It ,Iovvn tempt. oil iii
nlifillw(rir stare. r4 Ira$ Ibe lowrlit temp. at 111001 the
Pousd P.Mq- W-Ls X:-erl. P wpm it citwi-efluff. eutoctle (A +
B) willft clit"Itic Point b-IrOn, the cOutfutlell li4tild.0 branc.1t .
ut ta Theriattofrt+~
.ctkri p-i%wf. mix ix. luf A a ad B upon sirt (cring. meamitr"I
the-
tvillp. It-ackv]. re, this W" title ta fliti forinulloll
no tindumw6l ljiju~t phw~e- A phail djaparn of tht!
l
n
th
h%d
t
Ii
id vi
i
c art
sys
a
r
e
p
Itivell. 11101n.p.014,8 Q1111C TZ r, yieldrilCidthe.
the System 11-
ten,p. r aud cancia ot ~ pre ta;tdaW lor
nvidiraoilh! aeki (ilb. I-p-iminoberizoic n0d. 1-11. E-xi-'
nkruanillat: IV), I-p-pitroallwo (v)i v-succlaic Prilly-j
dr i-norbillfatul" V1 -0-1 It roall Hinz, IV-VT. Vt-p-e
cII1n,C;arl4Lr. VI-1-11
M N11, VT-3-amIaothLL(U1t.,j
V-111.111eicauhytItPle V111--mbomIrthollyiulfRivyl chloride"!
(13)( ItAx. and VII-FX. W. Linviberig, Jr.

Ed -011 -11"l-lum,"u'vioru rw-t f,
In# 4~
14 1
44* k ~Hl I
"I ueh,- ferll JIM4 It; I It 71t. 35 i
fLILk9a,
tir"Itlogm "icre trid cost oli cliel "Mpcv~nl
aud humarOk sintirt's 4*14 lo 1( 1 1 4
agents Otlatck. mcinic, otttbqllf:, and I'lelf-TOR: a '-, -;4
-and sulloarl rNWiloo). Itliad produ4k i4v ! it uturlil 0 1
Wirttt bf!~41tf Ii I,)& bit 4
hround In a somur ainj jn'CqVtjjjn CXW
note temp. SOW lailflul :joodwos rAQ~jo colvic l'JW Vb
pmductm d the maclion. 11ill of z
lovaHlit, I lKam ~
curve dam ~-q the 44bI -of I ifid euwtics ni 1~ a Irdl f
li I ore it f:
temp. coardl=tes W outertks 11 rl
pcerA. and the reactkin was cortlad cut in imiqll lentyr ~- I
c1li tOO IQW 110 fOWWOO 4 4 04UW PIXRM,~ 4
-uAld argAumterWls five cellu f 11
It
F-

5eparitlon of latolin trom wool fit. %~f, Kh. Mitzsclui.
1. Mishcv.,kaya, atid N1. h. Y.,V4,1 irrm"r"Tmatft"
CJ~C~71-1'11.11 Tit. ln$t,, K1111kOV). tr1Jbb4;w-7kirvToya
Pwm, 10, b:,,* 1, V.-OOMO.-Tw, ri,lhrid I, Vavd
obscrv~ition that yicid (1) .f lam,Ua ij ddtf. pi-finarily ~)r
t!je procrtitire employed. alid that I is Ln.
~~9 to , Icutraliza-
creaced from 31- %%her. a 2-itage i
tion proccss (11) Is used. U N descriLTA as folkw3-. cmde
L-nalln, scod. from vrml fat after trmttncnt with Bertluillet
salt and HSO,, is treated witla 0.57,; cAlchtcd sw1a WHO hi
i , and
Are th-n ittotralitol With W-111% NAOlt sol
t
calcined "Ia. After the rAdn. of pI. .. (lie fesul bit nu
heated, sepd., and the LarvAin Is %vwilw-f free of 5 op. treattcl
)ritli Inflascirial earth, and filtritod prior to stora e.

GLUZMAN, H.Kh.; KLTIJSHNIK, N.F.
Pondensation of glucose with hydroarematic ketones. Zbar. 016.
khim. 25 no.ll*.2118-2126 0 155. (XAA 9: 4)
I.Kharvkovakiy gosudaretwomW univermitat i Slavyanakly khl-
miko-mekhwdcheskiy tekhAikiim.
(01ficil'") MUMS)

GLU2MAH, M.Kh.; DASHEVSKAYA, B.I.
New compounds of suppository bases consisting of stearic enters.
Apt.delo 5 no.4:14-18 Jl-Ag 156. (XLRA 9:9)
1e Iz ][harlkovsko nauchno-iseledovatellskogo khimiko-farmtsayti-
chealrogo inatituta.
(SUPPWITORIJIS)

GLUZKAN, H.Kh,; DASHIVSKAYA, B.I.; ONITSEV, P.I.; BBZMM, F.I.
Water soluble bases for suppositories and ointments. Med.prom.
10 no.4:14-L5 O-D '56. (MIBA 10:2)
1. Kharlkovskiy nauchno-iosloclovatellmkiy khimiko-farmatsevtichaskly
inatitut.
(SUPPw ITORIM) (OINTHMS)

IL
74,
Imux 11tv OUMV00 tudling W 411, ad C
Outman ard V, 10, Rutwtvm~ ~Mm k1ov
CEE-557Mmi, WO. Aid. Asta). 105dj .1
c(mhrt: Nikiti,apluratta 6g
1223) is U%tl;l 1c III fitudy 4if eutectid ~Iwl
flog.. AnAl
of 26 b* cut -,)Y;tflD1. A tutihod of 0101
'T."N41 urpn4c
lying ffidiv%u.
Inixtum-3 with any. tittio. of: the mam
described.

AIM'

Owl. i f P i,lii
79
lo "t;
'i pl, ul 1~wojlaf g w i 11 1.41 1 H ital,
-------- --- --

-- -----------
USSR/ih&m,~dyn-a-mics- Thermochemistry. Equilibria. Physico-chemical B--5
Analysis. Phase Transitions.
Abs Jour : Ref Zhur Khimiya, No 8, 1957, 26178
Author :M.Kh. Gluzman B.I. Daahevskaya
N ;7
Title :it~~ ~O =~ertiea of Fatty Melts by Physico-Chemical
Analysis Method'
Orig Pub :Zh..prikl. khimii, 1956, 29, No 7, lo66-lo7o
Abstract :The fusibility diagram of binary and ternary systema of
fatty melts, the components of which were hydrogenated fat
(I), hydrated fat, paraffin (II) and lanolin (III), vere
studied. The existence of an interaction between III
and methylstearate (IV) or ethylstearate is shown. An eu-
tectic at 32-50 (6o% of IV, 30% of I and 10 of II) was
detected in the ternary system I - II - IV.
Card 1/1

Aouctiona with ivrtlcijatl,,n of nolla orrnide oulmtftw,-,-. Prcrt 2:
'iftort survoy of in. o roactiono ~thlch may ;.,i lon~-~~ -!-on n~i iylt.-,!.-
actions betweart solid (irganic substanceb. 71117?-185
Iq 17, (Chenical

.' Ah.; D.Yi.
Reactions with particilation of solid organic oubstaWes. kart 3:
Interaction between solid amines and solid mlelc anhydride. Uch.
za-pa MIGU 71:lFk?-195 '56. UILRA 10: F)
(Chemical reucti,~ns) Uninea) O[aleie anhydride)

I
Re%ctione with participation of solid organic substmes. Pe--t 4:
Method of determininp the reactivity )f aystews cobststing of two
soIJ:l ortanic substances. Uch.zap4 KIIGU 71:197-210 156.
(MLPA 10;8)
(Systems (Chemistry. N)
(CherAcal reactiors)

-GLUZM-N. M.1h;
-Oft-ftn"
Reactions vith participation of colid orp*nic substances. Part J:
Studying the effect of t~A easeoue phase in the proceas of Inter-
action botween solid organ!c vubstancen. 1:ch.zar, MIG13 ?1:211-222
'56. (KaA 10- 3)
(Chemical reactions)

N44 H is I; d4Pl I:lll~il:? III 'Mit" z -,, a j OtIf! j"If 7~ 1'.1 :14 1 11 !Ill 11 jj,j I 1 :1; ill I [III! I I I I IIIJI 1111kill I Iltit I t N Rt IM43SIRIt I IV' I IN 4~ I FRI I 0311:1141i. I IF I I HJ'dll Ill A I] fl I, A I IV All! I 141M,
GtUWO1?t ti. Kh.
reaNs. tM
III: r,,I: ,
-~r n,
X 5,
- - - - - - - - - -
1 7 T
ININICI WWII
IT W11111r, r .1
r, mt, ff ill" fl r IN 1 111, 5 1 A ~i

GLUZXAN. H.Kh.
e~w.-w W,-
Identification of glucomides fury1chromones, alksloids. and their
colts by determining euteotto temperature, Aptadelo 6 no,ltlO-14
Ja-F t57. (KLRA 10:3)
1. Is Khmr9kovskogo muchno-issledovatel'skogo khtmiko-farmetsev'tt-
chaskogo Institute
(AUTACTICS) (rHARMGOLOGY)

GILOU MAN DASHMVSK.AYA, B.I.
Vater soluble bases for suppositories and ointments based on
polyethylene oxides.Apt.dolo 6 no.2:73-77 Mr-Ap 157 (ML11A 10:6)
1. Is Kharlkovakogo nauchno-iseledowatellskogo khimiko-farmtsayti-
chaskogo Institute.
(ATHTIMIN OZIDW) (SUPPOSITORISS) (OIJITIOVS)

J
GLUZMAN, H.Kh.; LIVITSUYA, I.B.
Study of the interaction of solid sulfathistole and phtholic
anhydride* Hadeprom. 11 no.12:17-22 D 157- (IM 11:2)
1, Kharikovshy nauebno-Iseledovatellskly khImike-formstseytiche-
skly Institute
(SULFATRIAZOIA) (PHTHALIC AMDRIng)

-TT-
11 7
WIR-5
I WO-1
4;01
-1j
---- - -----
211
rv i Ij r
)t in wit
ur.
j~t
Liz
L
vIcytay Ui!d for tat I I
j A ~ jx
49, '(0956 - Aoabca D.,L) I
.11' v
ly i"- Ll ari
I t 4
Ilk! if
(I the ard o"mPA41 1 4 ji,a 'INO'k
-2E,
-----------------------------------------
17
71
~T
d i
-7 77

GI,UZKAN,.M.Kh.; DASHEVSKATA, B.I.
Studying the properties of fat malts using ph7sicochomical
analysis. Zhur.prikl.khlm. 29 no.?:1066-1070 JI 157. OURA 10110)
(Stearic acid) (Paraffins) (Fate and oils)

- GLUMAN, M.
Answer to the letter of P.M. Isakov. Uch. zap. JDfGU 82:157
157, (MIRA 12:9)
(Chemistr7, Organic)

GLUZMAN, M.Xh.
Reactions with participation of solid organic substanceo.
Uch. zap. MGU 95:249-275 157. (MIRA 12s10)
(Chemistrn Organic)

GLUZMAN M.Kh
--- 7-~~zu'
Reactions with participation of solid organic substancoo.
Uch. zap. KHGU 95:249-275 '57. (KRA 12:10)
(Chemistry, Organic)

AUTHOR: Gliizman, M. Kh. SOV/79-28-11-19/55
TITLE: Reactions Under the Coop.-ration of Solid Orlvinic
Compounds (Reaktsii a uchastiyem tverdykh organicheskik-h
veshchestv)XI.Transformation of 11-Aryl Amino Acids Into "'he
Imides Under the Influence of Temperature (X'I.Pre-
vrashcheniye 11-arilaminovykh kislot v inidy pad vliyaniyem
tp.-iperatury)
PERIODICAL: Zhurnal obahchey khimii, 1958, Vol 26, Nr 11,
pp 2987 - 2993 (USSR),
ABSTRACT: The authors devised a synthesis of the If-aryl amine
acids from solid amines and solid anhydrides
(Ref 25). The investigation of this reaction by
plotting the heat (Ref 26) and ki-ietic curves of the
acylntion process of the amineu under the cooperation
of solid compounds (Refs 27,23) made it poncible
to devise conditions that secured a quantitative
yield of the N-aryl amino acids and that aloo explaired
the role played by the liquid and gasoous phase in
Card 1/3 these processes. Based on the kinetic investigations

Reactions Under the Coo~eration of Solid Organic SOV/79~20-11-1~Vrjj-
Compounds. XI. Transformation of IT-Aryl kmino Acido, Into the Imll-del
Under the Influence of Temperature
and the heating curves it was possible to CILLS13iry
the influence of the temperature and the dia-ation
of heating on the degree of the transformation of
these acids into imiden. k COMP10W idOIL Of' tile
influence exerted by these factors an the inidation
process, which is necessary for the plotting of the
diagram of the amine-anhydride systems (Ref 31) as well
as for the working out of industrial acylation
processes of the --mines in solid phase (Ref 32), can
only be obtained by way of the investil-,ation of the
kinetics of the proce,s at different temperatures.
Therefore the autho--s inveatt-ated the kinetics
of the transformation of N-aryl amino acids into
the imides at different temperatures. The re-,ults
obtained are given in the table, and the imidlation
process in the course of time can be 30en in Aliguron
1-5- It wan shown that the velocity and degree of
the imidation depend on the otructure of the 11-aryl amino
Card 213 acids as well as on the basicity of the pri!-140'y ominea

Rcactior.3 Under t.he Cooperation of Solid Or.-Snic SC11/1115-22-, I - 1 , !- -
Compounds. XI. Transfor-lation of N-Aryl Amino Acids Into the Inides
Under t,,.e Influence of Tenpcl-ati%re
from which they had formed. The imid%tion alw--yo
bejina in tl,.e solid phanne, sozetimQa --t a temperature
that is far below the melting point of the i-ryl anino
acid. In many cases a complete imidation of the
aryl amino acid can be obtained in t,,e uolid phase.
Tiiero are 6 fii;ureo, I table, nnd 34 references, 12
of which are Soviet.
ASSOCIATIO111: Kharlkovskiy gosudarstvennyy univeristet (Khar1kov StLte
Univ:?rsity)
SUBUIT'I"ED March 141' 1957
Card 75/3

76-32-2-23/38
AUTHOR: Gluzman, M. Kh.
- - -----------
TITLE: Reactions of Solid Organic Substances (Reaktsii s uchastiyem
tverdykh organichakikh veshchestv) X, A Method for Plotting
Phase Diagrams for Binary Organic Systems Capable of Con-
secutive Reactions iz~usion (X. Metod sostavleniya diagramm
sostoyaniya dvoynykh organicheskikh sistem, pri splaylenii
kotorykh vozmozhny posladovatellnyye reaktaii)
PERIODICAL: Zhurnal Fizicheskoy Khimii, 1958, Vol. 32, Nr 2, pp. 388-393
(USSR)
ABSTRACT: Two modifications were performed in the method of H. Rhein-
boldt (Reference 5) and thus it was rendered suitable for
the plotting of phase diagramo of anhydride-amino-systems.
These modifications weres 1)Instead of fusing the components
the thawing and melting of the thoroughly mixed solid powdery
substances wa3 observed. 2) The thawing and melting was ob-
served not only in anhydride-amino systems but also in N-,a:ryl-
Card 1/3 amino-acid anhydride and in N-arylaminoacid ainine systems,

76-32-2-23/38
Reactions of Solid Organic Substances. X. A Method for Plotting Phase Dia-
grams for Binary Organic Systems Capable of Consecutive Reactions in Fusion
taking into consideration that in somt,- mixtures with melting
points near the melting points of the correspondingly lower
melting eutectics a heating up to not high temperaturos could
not lead to a reaction between solids. The tentative use of
the Rheinboldt method changed by the authors for the plotting
of the "thawing melting" diagrams of anhydride-amino systems
showed that diagrams for the state of binary organic systems
with chemical interaction can be plotted by observing the
thawing and melting in the thorouChly mixed powdery substancas,
without making it necessary to fuse the mixture. This offers
the possibility of plotting phase diagrams of such systems
in which consecutivo reactions take place during heating.
Such diagrams for 12 anhydride-amino systems are givent
phthalanhydride with n-toluidinet n-cbloraniline..o-,m- and
n-aminobenzoic acid; anhydride of amber with m- and n-amino-
benzoic acid. There 14 figures, and 7 references, 4 of whie~h
are Soviet.
ASSOCIATION: Khdkovskiy gosudarstvenny universitet im. A. M. Gor1kogo
( Khar'k6y State' Ublvirsity - imeni A* M. Gorzkiy)
Card 2/3

76-32-'2-23/38
Reactions of Solid Organic Substances. X. A Method for 'Plotting Phase Dia-
grams for Binary Organic Systems Capable of Consecutive Reactions in Fusion
SUBMITTED: November 23, 1956
~ 7 -
1. organic compounds--Chemical reactions 2. Organ1c compounds
--Phase studies 3. Organic compoxmds-'remperature factors
Card 3/3

UMNAN, H.U.; DASMSKAYA, B.I.; 3ODNYA. V-M.
Polyethyleno o3dde as a base for contraceptives. Aknsh.1 gin. 35
no.6:21 W-D 159. (MIRA 13:4)
(POLTITHYLIMS pharmacol.)
(CONTRAGIRITIS)

86326
gyfG/CO;'?/G
22-a9 B01 71] 076
AUTHORS: Gluzman, M. Kh., Dashevskaya, B. I., Dodnya, V. M.
TITLE: Preparation of Polyethylene Oxides by Folynerization of
Ethylene Oxide
PERIODICAL: Vysokamolekulyarnyye soyedineniya, 1960, Vol. 2, No. 12,
pp. 1832 - 1838
TEXT: Two methods have becn developed for the preparatioti of polyethyl-
ene oxides: 1) polymerization of ethylene oxide in the li-I-luid phase at
120-1500C and 15-20 atm, and 2) by passing gaseous et;hylane oxide into
alkalic solutions of glycol. The composition of polyothylene oxides and
their properties depend upon the ratio of ethylene oxide : rater and
ethylene oxide : glycol. The influence of the concentration of the cata-
lyst (KOH or NaOH) on the rate of reaction and on the properties of the
polymers is illustrated in Fig-5. The maximum value for the molecular
weight of the polymerizate depends on the nature of the catalyst and tile
purity of the monomer., The rate of polymerization in the autoclave depends
an temperature, catalyst concentration, and conditions of contact between
Wd
12/013/019
S/1
Card 1/2

86326
Preparation of Polyethylene Oxides by S/19 60/002/012/013/019
Polymerization of Ethylene Oxide B017YB078
monomer and catalyst. The rate of polymerization in a colunn decreasee
with an increase of the molecular weight of the polymer and with a re-
duction of the catalyst concentration, Two mothods (if 1)uvil'ying oommor-
cial polyotbyleno oxide with ion oxchangeru and by "loctrodialysis have
been investigated. Polymers with a molecular weight of 4D00 were ob-
tained. There are 8 figures, 1 tableg and 20 references: 4 Soviet, 2 USp
8 German, 1 Britishq and 4 Swiss.
ASSOCIATION: Kharlkovskiy nauchno-issledovatollgkiy khiiidl~ofarmatsevti-
cheskiy institut (KhartkovCliemicopliai-~iat.-euti(,aI Scientific
Research Institute)
SUBMITTED: May 23, 1960
Card 2/2

B/153j6O/OD3/02/17/034
B011/3006
AUTHORSs Gluzman, M. Kh., Millner, R. S.
.1-1--' ".1, - ---'
TITLE: Investigation of Interactions in Systems Composed of Solid
Amines and Sucoinic- or BenzoiO e by Means of
Beating Curves _~ahydriL 11
PER10DICALt Izvestiya vysshikh uchebnykh zavedeniy. Xhimiya i
khimicheskaya tekhnologiyal 19609 Vol, 3p No. 2, pp. 305-311
TEXTs The authors investigated 24 binary systems composed of solid acid an-
hydrides and amines by drawing the heating curves. Twenty-four acid asides
(Table 1) were obtained by this procedure. The authors describe the method
of plotting the heating curves of organic systems. Mixed equimolal amounts
of acid anhydride and &mine were heated for 20 min in a glycerin bath at a
rate of 0-500/min. The analytical procedure and calculation is described
by M. Kh. Gluzman in Ref. 4. After crystallization from alcohol, the sub-
stance had sharp melting points which did not deviate from publication data.Of
Card 1/4

Investigation of Interactions in Systems B/153/60/003/02/17/034
Couposed of Solid Anines and Succinio- 20111DO06
or Bonzol6-. Anhydride by Means of
Heating Curves
these substances the following have not yet boon d*soxited in publicationes
(4-chloro-Phsnyl~ succinanio acidv (3-oarboxy-phsnyl)~suoainsmie aoidp
succinyl-2-aminothiaLzolog sucoiniY.1-4-afflifloantipyrins , bensoyl nor-sulta-
zole, and benzoyl 2-a-Inothiazoloo Plgo 1 gives the beating curves of the
systems composed of succinio an
,~ydrids and the following aminess p-tolul-
dinev p-ohloro anilino9cK_ and IS-naphthyl-aaineq o-jm-, and p-bs1Lzo16,.,
acidt o-, a-, and p-nitro-aniline, nor-oulfazole, 2-aminothiaxole, and 4-
4~minoantipyrine. Eleven systems consisted of benzot6-; wihydride and the
above-mentioned jamine I except for the systems containing 4-amlnoantipyrine
and m-a-indbenzoUc a:id (Fig. 2). Since hosting of solid acid anhydrides
with solid anines in nearly all oases given practically quantitative yields
in-sucoinamides and benzamidoe, the authors suggest this method for prepar-
ing amides. On heating, the reaction sets in in the solid state (except in
the systems Noo 1 and 4, Tabli 2)* Most amines reaot more vigorously with
benzoijt.: anhydride than with s*ooinio wihydride (Tables 2 and 3). Systems
containing o-nitro-aniline in the solid phase are acylated to atmost
Card 2/4

Investigation of Interactionsin Systems
Composed of Solid Amines and Succinic-
or Benzoic,~ Anhydride by Means of
Heating Curves
en
S/153j6O/OO3/02/17/034
B011/BOO6
components. There are 2 figures, 3 tables, and 32 referencest 4 of which
are Soviet.
ASSOCIATIONi Institut khimii Kharlkovskogo gosudarotvennogo universitota
imeni A. M. Gor'ko&j; Kafedra organicheskoy khinii
(Institute of Chemistry of the Khar1kov State University
imeni A. M. Gor'kiy, Chair of Organic Chemistry)
SUBMITTED: July 7, 1958
Card 4/4

S/I 53/60/003/004/024/040/U~
B020/ t,054
LUTTIORS: Gluzman, M. Kh., Millnor, R. S.
TITLE: Study of the Process of Acylation of Solid Amines With
Solid Succinic and Benzoic Anhydride Under lt3othorwal
Conditions
PERIODICAL: Izvestiya vyashikh uchobnykh zavedeniy. Xhimiya i
khimicheskaya tekhnologiya, 1960, Vol~ 3, No. I,
pp. 684 - 690
TEXT: The authors conducted a series of experiments in which the binary
system anhydride - amine was kept under isothermal conditions for a time
sufficient to obtain constant reaction yields. This made it possible tr,
choose the optimum conditions for the synthesis of amidea from solid
components. The binary mixtures investigated were composed of sucoinic
anhydride and the following amines: a- and P-nahthyl amine, :%-, M,-,
and p-nitro-aniline, o-0 m-, and p-aminobenzoic acid, p-toju.jdine,
p-chloro aniline, nor-sulfazoll 2-aminothiazole, anti 4-aminoantipyrine.
The same amines, except for m-aminobenzoic acid and 4--aminoant~Lpyrine,
Card 1/3

Study of the Process of Acylation of Solid s/1-3/60/003/00,~/0241040/,U,
Amines With Solid Succinic and Benzoic B020/BO54
Anhydride Under Isothermal Conditions
were also present in the systems containing benzola anhydrJde. The au-
thors studied the behavior of the systems in the solid phaa,'., at th,~
melting points of the quasiequilibrium and equilibrium eute-:;Itic &nd J
the low-melt~lng component, as well as at temperatures 5-10oc lower
those of the phase transitions. At least five "yield--I-imell isothezms
were found for each system in this way. An analysis of these irotherni.
shows that in known approximation all isotherms can be divided Into
four types (Fig.1). The effect of temperature on the rate and yield of
benzoylated and succinated amides is shown in Fig.2. Ar. inTestigation
of the state of the systems at constant temperature pormits an estima-
tion of the effect of eutectic solutions and melts of the components on
the reaction yield (Table I). Table 2 gives data of the yields obtained
on heating the systems to a temperature ensuring the formation of maxi-
mum amide amounts, and by keeping the component mixture undor isothermal
conditions. If the heating curves and the isotherms for tKe systems of
solid anhydrides and aminds are known, it is not only possibls tc, de-
scribe the detailed conditions for the amide synthests, but al~;t: t~~
choose the optimum conditions for obtain"Ing purp pro(lu,~t,-, ~ri
Card 2/3

Study of the Process of Acylation of Solid 3/153160/003/004/024/040/XX
Amines With Solid Succinic and Benzoic B0201BO54
Anhydride Under Isothermal Conditions
consideration of the properties of -jaction components. The paramel.ers
of temperature and time given in Table 2 are sufficient to synthesize
the 24 amides mentioned in the most favorable manner, There are 2 fig-
ures, 2 tables, and 11 references: 8 Soviet, 1 US, I German, and
1 Polish.
ASSOCIATION: Institut khimii Khartkovskogo gosudarstvennogo universi-
teta im. A. M. Gor1kogo, kafedra organicheskoy khimii
(Institute of Chemistry of Khartkay Statis Univer3lty
imeni A. M. Gorlkiy, Department of Organic Chemistry)
SUBMITTED: October 16, 1958
Card 3/3

GLUZKAN, M-kh., LEVITSXATA, I.B.
Investigating the process of mtbylation of cellilose. Zhur.prikl.
khiz- 33 no-5:1172-1177 Yq 16o. (NIRA 13:7)
(Cellulose) (methylation)

GLUZMAII, M.Kh.; RUBTSOVA. V.P. (Khar Ikov)
Butectic melting of systems composed of organic salts &td acIds.
Zhur. fis. Idds. 34 no.l2t2742-2747 D 16o. (MIRA 14:1)
(Natectics) (Acids, Organic)

rjLIJZM, MoKhos dotsent; LEVITSKAYA, loB.j kand,modanaulcl BASHURA, G.S..,
nauchnyy sotrudnik
Carbmtymethyleellulooe sodium as a bydrophilic ointment bass.
Teet.derm.i Yen. 35 nb.4140-" Ap 161. (MIRA 1415)
1. Iz Kharlkovskogo nauchno-iseledovatellskogo khimiko-farma-
toevticheskogo instituts, (dir. M~A* Angarskaya)o
(037MMM) (CEUBLOSI)

GLUZMAN, M.Kh.; LEVITSYAYA, I.B.; BASHURA, G.S.
Methulcellulose as a base for ointments. Medo prom. 16
no.1:21-24 Ja 162. NIRA 15:3)
1. Kharlkovskiy nauchno--issledovatellskiy khimiko-farmtsev-
ticheskiy institut.
(CELLIADE) (OINTMENTS)

,qLUVW, M.Kh.; DASHEVSKAYA, B.I.
Use of surface-active substances in pharmacy. Mod. prom. 16 no-3:15-
20 Mr 162. (14IRA 15:5)
1. Kharlkovskiy nauchno-issledovatellalciy khimiko-farmitsev-ticheskiy
institut;-
(SURFACE-AGTIVE AGENTS) (FILARMACY)

GLUZMAII, M.Kh.; BASHURA, G.S.; DASHEVSKAYA, B. I.
Anomaly of the viscositu of polyethyleneoxide and the effect
of certain medicines on it. Apto delo 12 noo5sV-23 S-0163
(KIRA 16M)
1. Kharlkovskiy nauchno-issladovatellskiy khimiko-funatserti-
cheskiy institut.

GUZMAN, MI.Kh. [Illuzman, G.S. R'.3.j
Test:Lng ointments propared with hydrophilic ba.,,co by it pendul=
consistometer. Faxmatsev. 71itw. 11", no.2:27-33 163. I,/:io)
1. Xhavlkovskly naucluic-isoleelovatallakiy
institut,

GI,IJZMJtN, M.Kh. [HluzirAn, IA.Kh. j ; BL-MINA, I Nuhurp., 1!.S. I
Preparation of a stable suspennion of corinal. Farmatisev.
2hur. 18 no.4:31-34 163, (MTPA M7)
1. Kharlkovskiy nauchno-isaledovatellskiy k)dmI.ko-famataevticheskiy
Institut.

kand. khim. nauk; BASHURA, G.S.; GABRILOYAN, D.A.
Using a pendulum type cannistometer for tenting tooth pents
with a water-soluble base. Naol,-Shiro prow. 29,n*#3t2S-3l
Mr 163. (MIRA 16:4)
1. Kharlkovakiy nauc)v;o-iseledovatel'skiy khiniko-farnatmov-
ticheskiy inotitut.
(Toilet preparationa-Tenting)

GLUZMAN, M.Kh.; BASHURA, G.S.; LEVITSKAYA, I.B.
Purification of technical sodium carboxymethylcellulose.
Zhur.prikl.khim. 36 no.6:1258-1263 Je 163. (KLRA 16:8)
(Cellulose)

Corsistency c!' :~In'rncntc; ;in,4 its detfurr'n;it! 7:.
Avt. deio 13 no. Fy-'p 164.
1. Kharlkivskiy
In.-Itj tut,

G 11 U Z rul N tfAsllmo 1) .
Rheological methods used in evaluatIng th,~- romnistency of
oIntments. Report No.2. Apt. delo 13 nc,.0160--~!,' JI.-Ag 164.
(MIRA 28s))
1. Kharlkovsk4y nauchnc-!sPledovatel'6kJy kh--'Mlkn--f&rmqtqevtichesk!y
institut.

1 6T
LCCE.SSTON NR.- AP5019287 tJR/0332/65/000 007 0020 '100
660'. V35: G6 1. 18 l.+,547
4.7
M. Kh. (Caudidate of 6~evaeeil _isai`
AUTHOR:- Gluman
TIT LE Evaluation of the surface-aeUve proportlea 4f cortfiln OM4 0.0r41, t1jWMA
cellulo;e ethers Report No. 1. A
Maslozhirovaya promyshlennosti, U . 71 1906 20-22
ISOURCE.
TOPIC TAGS: surface active agert, emulsifteri thLakerdog a&nti fn
I Ojlyji.4~; U1080
od,
Win carboxymethylcellulose
s
AMTRACT: The study deals with surface active xg~ntfj (SAAB uao I :~l if. ticiii
r p,iq n"W('Pu
13urposes -abroad and-intbe cosmetic and food Industry il
i'l-volved the use of specia:li-y----p-r-e---p--a-r--O-Omutstang of-Vaseline-t--, "tar of Intl
fish fatj which wzre stabilized with 16 MA aM ~ i ojiture4l of ~thw I 11111a-104 1
I.
and emulsion thickeners used were aqueous solutt , I it t
t1s': of 1~0 1K 1 6 1 tu
1h
cw- )x raothylceBulose (sodium-CMC), caoable. of fnereisinj4fl"im~ OIL" m I a
~posq ji f
_.A and thus farming proWtive hydrate fUms at,the iml6rfAdej. Tho e J., vb J.,Iro r Jet
of the SAA In the'soluble cellulose effiers wibre dettirphiod. lbd 01 1. . 1104.1 or~ ie 5
solutions of sodium-CUC changes Insignificantly %v$th c6cenitatti :1 Ocifii to t!
!A~ A

A629A 0-65
F T_
ACCESSION NR: AP5019287 ri
face terision of Yvator; the greatest change is observedwhe'n' i< ~Auip Ila
raised to 50C (Che r3urface tension of volations of ill ctmee4ratio"s, i~ lien 4 ;~)t a/,cm)!.
jfienco, sodfuni-CNTC may be considered to be a surfapo-llj~.Otivo Fniti iltioles of i
the, sartace tension of MC solutions as a fluxotion of concentraWin, biiil I lerailt jxeV raid vi j-
cosity 4-haracteristics showed that MC Is'a weak surfactant, Nomdij 1A 11 M,'(' , afflii
sodlum CMC are used as thickening agents In the prep,,vatibn oflonitill itons 114), aq$i~ they
aisaAhe-_viacoait""ht A'sWral _M0411 -0rip,
-011 UM T
-table.
:L
lei3kiy in.
ASSOCIATION: Kharlkovskiy nauchno-issledovateltwy girl, akseiff
stitut (Kharlkov Scientific Research Chomico-Pharma&sutlcal 1j:
g1j.D At :00
SUBMITTED: 00 ENCLh 00
-NO RE F SOV: 002 -IF
OTI R: 0071
T
r
a v
Card 2/2

1!. fil uzmrin. N%v I 1. 13'.." 1 ITIRA, '~:V AY I. - 1 .3.
itudy 1T .1t.ructkiral !lid 1110-~Jt)rtclll wntl~-tob.hje
collillo.'m ot.1101-:1 Iv V11 I. I
..,Jin (100TIVO vf volym,,riZation. Far-matneiv.
zlhur. 20 nen.]:.16-126 'E5- (V:"A 18-20)
1. )(h,1r1kovskV nqurhn(.,-Igi3lRdovqtAll,iliv Pdrilkv
in a 0 tut,

GLIOWN) M.Kh.; DA.MVSKAYA, B. I.; FRIDMAN, G.M.
Preparation of sorbitan monoo3ters ) an,.I t.1flix
hydroxygthylated products (tveow). Zbur. prIA), khLm.
38 no. 10:2319~2325 () 165. (MIFA 18:12)
1. Kharlko7skly muchno-issledowtell I ski y klilmilco-farwitsev-
tichaskiy Inatitut. Submitted OctoWr 30,0 196).

ACC NR: AP?OO7t30,9 SOURCE COD~-;': TJ?,/CjOaO/6?/Cl~0/001/02Vj/O2O9
AUTHOI: Gluzmant M. Kh.; Zaslavskaya, R. G.
ORG; Kharkov Scientific Rosoarch Chomico-Pharmaceutical Institute (Khar'kovPkiy
nauchno-issledovatellskiy khimiko-farmatsovt:Lchoskiy inutitut).
TITIE: Kinatics of phthalylation of acotyleellulone and viscosities of acetyl-
phthalylcol-lulose solutions
SOURCE: Zhurnal prikladnoy khimii, v. 40, no. 1, 1967, 2o6-2og
TOPIC TAGS: cellulose, viscosity, phthalylation',
ABSTRACT: In order'to determine tho optimum conditions for preparing acctylpht6lyl-
Ccalluloso (APO) which is soluble in organic solvents and weakly alkaline media, -a
study was mado of the kinetics of phthalylation of acetyleelluloso (AC) containimg
27-3eo acotyl grouDs at molar ratios of AC to phthalic anhydride oqual to 1:3, 1:5
and 1:8 and temperAures of 60, 80 and 1000. The highest degree of substitution by
phthalyl groups was obtained at a phthalic anhydride conWit of 8 moles per mole of
AC at 80-1001D. A study of the solubility of APC in mixtures of two organic solvents
showed that it dissolves bast in mixtures containing equal amounts of chloro derive-
tives of a hydrocarbon and alcohol. In mixtures 'of chioroform and dichloroethane
with alcohol containing 5% APC, addition of alcohol first leads to a sharp increase
and then to a decrease in the viscosity of the solutions. In dinethy1formamide, an
i Card 1/2 UDCt 50.40.82_

,.a!, . ITZ, "
); FA -1-7 ?'C!!, F. -',. , -': :'L . . '. ." I
C, L 1; Z: ';J,- I 11h. (FI-I '-I ~, -
-I. I- , -, ;):. ,
Improvement of IYZ boilers with 901110 t/fx. Ovarrat?,Ve
capacIty. D.ergetik 13 r.,o. 1-21-13 D 161; 1~,:l)

plffi~ - ... - I 1 1. , I'll pit
/StrafikeviZ, A. M., and Gtuzm Aberratious of
a'A I F/W
relativistic electron beiMMS, . +en 24,2271
-22844
(1954). (Russian)
An electron beam is defined as the tolalitY Of moving dec-
trons having the same initial velocity and trajectories clooe
to an axial trajectory. RelativistIc equations of motion am
derived (or a wide bearn in an arbitrary electrostatic field.
In this treatmetit the aicis need not be a straight line, but
may be bent. e.g. in the form of a helix. The systems with
a bent axis are of special interest since they may give r6e
to negative chromatic aberration. The spocial cases om-
sidered am the relativLqtic equaiioni of motion in an axially
symmetrical field, a flat fitid, the field of,it cylindrir-d lent6
and the field of a cylindrical coadenser. Image aberrations
are computed for the relativistic case (6- an axially qqn-
metrical lens and a cylindrical lens. f. B. Rosenth4d.
J
PIT

GLUZRAN, S.S.
Use of control calculating machinsa 4.cr ",he regulattion of the
parameters of technological proces3sa., Khim.proj*. no,12:920-922
D 163; OMIRA 170)
i
I

I ..V-- I 1$7t t1 r1l NF f I I r 'k I ;:1 1 1111 ;t:: I ilif 1111.111f I I Hill WHO I ["it WIM
M111114111filillill 4V 11111 111,11friffitil
IKII M "IF11111,011
'il~ 11 11 11 ulml lit I i I gm illf
FRI!
-IT (d)/&--Y (n)-2/fill' (I) pa-VPC-4 pt-i
L3858?~65 F.
XUCMZSM-N NR: AP500593Z S16 I

AUTHOR: -Gluzm4n, S-. S. (Engirfeer); Krayno .!..V. Ni 6 a
..................
-
Jibl of ce:01A T-7
ifl:4
Iifiit~ 6` 1. (Engineer)
sciences), Martyu;

TITLE: Selecting the number of digiti~ for out
put
rn
t
digital controller
SOURCE: Pribor-3stroyeniye. no. 2, 1965" 1

TOPIC TAGS: dillital controller, digitall proceas -C'01 tiol la
'j :01r, i C
c~irttra
t
automatic control design, automatic con"rol sy,pta,:m, qjut09j'-l q ic I; irl, rp~- theq *
ABSTRACT: Ushig a model wliiclk simulated ALdWtal Gracie
l !da C4 I 14-0i" tile l e *it C ,
of level quantizatlon of the controlling s;-ignal upon, the L-antiri l~~ pri: 40 $0 Was
ev3luated; also. a minimurn number of digits:irt the c6rltkil kto i
which still did not impair the quality of control Wis; deternld h6d. I I i.avek J gati on
was performed on a "Kataliz" analoS computer to whi(zh a:! ej: J; o4l I C. ay!",line H' (f a, li
Card /Z
!MIMI 1111111

L! 38589-65
ACCESSION NR: AP5005937.

added; the signal was level -quanti red 4~ a: no 6'finq~g,r 00.6i
1: .,n F W.4 nusn ~ar of
stops at its outptA ahowed the nurnbcr of dig6o. to rlidu6i- :i"Ie ~ 6! liltizae Of
sustained cycling that accompanied a feiv-digk sy*tem"* th'6
' abnt il
algorithm was changed; instead of calcxiLating
~ the conOol:- n~ p
!q oiitiba, ifs
speed was calculated; a stepping tnet.or was ui~sed as ai~ vO u ~a
h' ng~ ViCIP. tkI.6 Lr

noni s ornetric -digit code conversion of, the control! signM. q0z
ktO :cl n~ t1401, t !bit-
for greater errarsi rnade poosible a high-stattc-atcurk~.,O it et I Ni Ith ~m f ei i d
in the output devices. (10. G. Ehruzhinip took part S'n t~o alt 3ati~
r 9 !at ~UgAtJ3. L,
automatia-control Sys tei_za.W_0r_ij;_. -air_t -hais t5rieA~es' 15 roir
4 10.lam ~
41114RtabiL
t8.
ASSOCIAVON: none

SUBMTTED: 00 ENCL: 0
0
Co
:D.P. 11
NO REP SOV: 001 0 T H9, (U 00.2

z
ii-7 7- 7
1
1~q T_

. ~ ( ) ' , -" .I C. '- .
-Jud -~W X
-ACC-M-1~6010021 SOUR'Ci'(jODE- uAAif6X~/oo67&i/0003/0006
AUTlIOR: Gluznian, S. S. (Engineer); Druzblnln, 0. G. (Engineer); 34artyushb, Yo. L
(Engineer)
ORG: none
TITLE: Modeling of industrka digital controls on analog 6omputers
SOURCE: Priborostroyenlye, Do. 3, 1966, 3-6
TOPIC TAGS: automatic control design, control simulator, computer control system,
automatic control equipment, analog computer, digital computer system
lip
ABSTRACT: Digital control computers are being utilized as multichannel regulators of tech-
nological processes. The authors discuss the circuits of such a multichannel system, analog-
to-digital conversion, and the difflculties encountered in the design of such systems. The
difficulties involve the analytical determination of time optimal control, the tuning parametexq
of each channel, the influence of the level quantivation on the control process. etc. Since meir
such problems can be studied relatively simply on analog simulators the paper presenta and
discusses, among others, the block diagrams of a fixator model, a control-law components
model, a variable coefficient block model, and a signal level quantLzation block model. Some,
#4 4 4
Card 1/2 UDC: 681.142.334

GLUMU) V.
The works of the technical library is organized by the Scientific
and Technical Division. Muk,elev. prom. 27 no.9-.27-28 S 161.
(MIRA 15:2)
1. Prodoodatell Soveta porvichnoy organizataii muchno-
tekhaicheakogo obshchootva khlebnoy bazy No.80.
(Ticbnical libraries)

GLUZMAN, V.
More on bucket conveyor bolts. Muk.--elev. prom. 30 no.3:30
Mr 164. (MIRA 17:4)
1. Glavnvy inzhener Kharlkovskogo mellkrupozavoda No.2.

LOYMVA. A.N.; GLUZHAN, V.S.
"Oftffivftwm.~
Remote resui-te"BT "radiologic and opera tive therapies of uterine
cancer. Trudy AMU SSSR 21 no.4:81-86'52. (MIU 10:8)
1. Iz ankologiOlaskoy kliniki Sverdlovskogo mauchno-insledovatell-
skogo Institu.. fisicheskikh setodov Ischenja 4zav. - prof. L.K.
Ratner. dir. - kandemed. nauk To.I.Milrutias
OTBRUS. neoplasms.
radiother. & surg., results)
(RADIMTHIRAPT, in various diseases,
cancer of uterus)

1 1, 1 khonevi --~l
C' 'hurilalllvkh t Y, Voi. 44, Yzls'-va, 19 (1
L L 4,

GLUDUN To. 3;MMARIYAN, To. A.
Bloelectric characteristics of sloctroshok. Sh. nowropat.
palkbiat., Mosima 52 80-3:17-21 Mar 1952, (CUM 22:2)
1. Candidate Medical Sciences for Glusm"s 2. Of the CUOIC
for Borderline Condttinns (Head - Prof. A. L. Abambew-Woustantinovokiy)
and Department of Iftectrophystaloa (H*M -- Senior Scientific
Associate N. V. Semenov) of Kiev Psycbeamurological Institute
(Direetor - P. S. T&ras*nko; Scientific Assistant to Director
Prof. D. 1. gantkovskiy, Active Member ANS USSR).

GLJZMAN,_,ye.B., kand.med.nauk
Hypochondriac 8Yndr0MGs f0l-10winrlprevlous rimaroln itl*us diseases.
Vop. klin. n&vr. i sikh no.Z304-310 158. 14:10)
(HIPOCHWHU) immous SYSTM-OISILAW

GLUZMAF~ Ye.B.., kand.med.,nauk
Hypochondriac reactions and the development of hyNahondriu
Wach.delc no.2t89-93 F '163. (MIRA 1635)
1. Kafedra psikbiatzril (zav. -- prof. Ya.P. Frtuakin) Kiyevskogo
meditBinskogo instituta i 7+.orava dorozbmayu boltnitna Yugo-
Zapadnoy zheleznoy dorogi.
(HYPOCEMRIA)

KAZAUVICIIP R.L.; GLUMVI, Ye.B.(Klyev)
State of the peripheral blood circulation in dieucephalic
syndromes of different etiology. Vrach. delo noXzUc~-
.14 Ig 163. (RDA 16.9)
It Dorozhuaya bol'rLitsa No.1 i Dorozhnaya bol'aLtsa No.2
Yugo-Zapadnoy zheleznoy dorogis
(BLOCD-GIRCUIATION) (DIENCEFMWI;--DISWES)

GLUZKAN, To. 1.
- --mommeno
Industrial and technical propaganda at the Petr Anistmov Factory.
Tekst.prom.17 no.1:48-419 Ja 157. (mu 10:2)
1. Zametitel, predeedatelys pravlonlys klubs imeni X-lett" Ok-
tyabrya pri Leningradskoy pryadilino-tkatakoy fabrik" iment Petra
Anistmova.
(Leningrad--Textile factories)

BARAYANTS, A.A.; SMILLER, M.R.; KOLESNIK, M.K.; BALYUK, 0.11,; SIHAWKIY, N-ye-p
kand.med.nauk;-.PjtqZ~lAN, Yu.D.; WDVIKO, G.D., kand.zed.aauk; AKDIUJA,
Ye,A,p promyshlennyy vra"c'h-'SIDENKO, K.I.
Discussions. Vop. travm, i ortop, no.13:47-60 163. (MIRA 18:2)
1. Glavnyy vrach lechebnogo ob"yedinaniya shakhty "Dolinskaya",
kombinata "Sakhalintigoll" (for Barayanta). 2. Zavedik-vushchly
Yuzhno-Sakhalinskim gorodskim traw ',lowicheskim Punktom (for
Smiller). 3. Kholmskoye upravleni)e stroitellnoys upravlenive
Sakhalinshakhtostroya (for Kolesnik). /#. Doverennyy vrach
Dorozhnogo komiteta professionallnogo soyuza rabochikh
zheleznodorozhnogo transporta (^ir Balyuk). 5. Irkutskiy
gosudarstvenn,yy nauchno-issledcvatellskiy institut travmatologii
i, ortopedii (for Sinn'gkiy). 6. Starshiy inspektor Gosudarstvennay
avtomobillnoy inspekisii (for Gluzman). 7. Leningradakly nauchno-
issledovatellskiy institut tranmtologil i ortapedii (for Radenko).
8. Glavnyy vrach meditsinskogo ob"yedinoniya goroda Shakhterska,
Sakhalinskaya oblast' (for 81donko).

-7,
GLUM . Zhge, inzhener.
ew
- !1%
, OW
Utilizing the heat of circulating water* Imergetik 4 no.11:23-
24 N 156a (MLPA 9: 12)
(Feed water)

IF], 111 PIEK, 1 -14: 11:;1 '1 1 1.1 ;-T11111 11111i1: 111111111 KIP pl'-
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r,"a rv*oba- n=Zo. bem1nd -MAch rt c. m6
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MIT MI ........ .... 1.

GYTZMAN, Zh.Z., inzh.
1'. -
Self-regulation of the discharge of condensate ;u7T;.q. Rlek. sta. 29
no.7.-26-28 Jl 158. (MIRA 11:10)
(Steam turbines)

Trukhanov, A. A. , Shershov, S. F. , Rozeman, A S. , Kheyster, 1. E. , Gluzuriov, A. A.
and Gludinskiy, P. G. Participated in a discussion on the "Waste of Metal and Decreasing
the Power Losses in the Electrification Syster, of the USSR"
Loscow i o ;Qr 1--stitute jii-jn -,0V
19 -4
SO: Elektrichestvo, No. 5, 1947;&-27POl, 14 Sept. 5')

lp lalilptip Ill! vir, Y IMI fv'.T~' , !I 1! 41, 111 Fll.,, ql ViU ;ift 1011,
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L 55236-65 EWT (m)/E PF (c I /EWP Pc-A/Fr-A;, Ril
U=SION HRI' 0501 44/644-
5565
w
AUTHORS: Skripkov L, A.; Glyadelova, Vo G#
TITLE: A method for obtaining N,U'.'di. 1.n-p~ Irleal 3431amine lag 12*
alk4 it
7 9
.900
150521
ovj nom Opi
SOURCHs Byulleten' izobreteniy i tov=Vkh znok
,TOPIC TAGS: pherWlenediamine# dlWlationj catalpitj aliph !a 8!
ipol,vethyleneg inhibitorp rubber
UBSTRACT: This Author Cortificiite presents a method fl.or ab
Cq)-alkyl-n-pheny' enediamine by alkylating ff-phenyleaqdis;q~;,d at! 1l, 4izjj
tLmperatw-e in the presenwi of a catalynt. T si. .~Ich t I " ! thl pro :080~
Mpli, W jud of I
nozzal stmoture: 31 a~ -the 0 k.71 't-
a mixture of aliphatic alcoholn C C of I~a U
7
Tho pro(luot,ob! ej the
lirig agenti, and Ni-rhenium as the catalyst. tj4n tij
=,Id or V! low-prJu surlit
may be used as a motor fuel atAtbilizert ati the ttemostabi 1,
,ethylenep d tor of the nitre T~' ;Rae,
ax 0
po1j as an inhibi ogen aging 0 i4 pi 4'e
gn
ASSOCIATIONt none
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55236-65
1
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Acass"Off IM: AP5015565
SUBMTTEDs .25Doo6l ENCL: 00
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