SCIENTIFIC ABSTRACT YULDASHEV, K. - YULIN, M. K.

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• Collection: Scientific Abstracts
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• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT


S., ii~er Agric (uiss) M.-w pl=tinZ of lus =-~s
gatt,-d- -A ul-d-3- o-fpvndng cotton Md corns -ii, `U,,vak SSR. 11 Tanh-kcii t,

YULDASIEV. K.Yu.-. TSUKEIGANIR I.F,
Reactions of ph-aii7flacetylem and -2-mtW-2-phenylacatylens vith
anisole. Zhar. or. khim. 3.4no.8:2647-2652 Ag 164.
(IURA 17: 9)
1. Tashkents-dy gosudarstvennyy universitet im. V.I. Lenina.

ATAMMOV, E.I.;MWMT'X&n, AAJ BUDMIll, MI.; YULDASHEV, U.I.;
SHAMSUTDMOVA, R.E.; YMMAMV, X.Yu.
State of some metabolic irdiceD in peptic ulcor of the stomich
and duodenum and the effect cgi them of hydrolynate them-,.,,
Terap.arkh. no.7:85-91 .11 162.
1, Iz kafedry propedeftild imutrennikh bolezney (-.ELv. -chlep-
korrespondent Z12-7 SSSR i AN Uzbekskoy SSR prof. E. I. -:')
pediatrichookogo i nanitarno-gigiyenicheBhogo frJailltet.-v TzLr~.-
kentsko o meditsinskogo instituta.
f=C ULCER) (PROTEDi HYDROLYSATES) (11MCGEN IMZTAXIL'S")

MMATIYAN., A.M.; YUIDASIMV., x.yu.
Characterlotico of tI-x am-irso jacrd 05.-tticrA r
4. ,f
OMP
sate' produced by Contral Inotivatij of -the Ordr.,r (,f Lon1r, or
tology and Blood Transfusion. Probl. pmat. i peral, krovi 10 no.,:
52-55---Y- '64- a 1"A 19: a
1. Fafedra propedevtiki vnutrennikh bolezney (mr. - chlexi-korrea-
pondent ANN SSSR i AN UzSSR prof. E&I. Atakhanov) sanitarnb-gigiye-
nicheskogo i pediatricheskogo fakulitetov Tashkeritskogo meditsinskogc
instituta.

-t~~ r s
Per i Cad 1 6
A T, F,r 4 2
-4&2! ca r:- 4-e
C,Ud rt
e a 41 ir,.-
,mJ e an "-rc-
x-e affe~-~-,
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is ey

AUTBORS: V.- Kh. YJ COV/79-29-2-15/7,
Vuldashe
R. A.
Zakutskaya
-,
,

TITLE.- Nitro'anizole With Chloral Hydrate
Condensation of o-.
troanizola a.khlorallgidratom)
(Kondensatsiya o-ni
.
PERIODICAL: Zhurnal obshchey khimii, 1959, Vol.29, Nr 2, pp 429-431 (USSR)

ABSTRACT: 0 enol (Refs 8,9) and o-nitro-
The condensations f o- and p-nitroph
anisole with chloral, hydrate (Ref 10) are kno-sn among the direct syy,-
theses of nitrodiaryl trichloroethanen. D. A, Shirley obtained 'Y
-only~ a -y--i-eld -of -12%_1 .1 1v_trichloro-2,2-di-(4 -3-nitro-
-methoxy
phenyl)-ethane (II-) from o-nitroanisole (0-5 mol) with chloral
hydrate (0.25 --201) in the presence of concentra+ed sulfuric
acid (50 gr) and 201,~ oleum (100 gr). No secondary product-9 -f ox-m-
ing in this condensation are mentioned in this connection On
Bynthesizing trichlorinated carbinols and on investigating their
reactions the authors studied this condensation more closely On
varying the quantity of sulfuric acid and its rate of add:.*~_Cri
they obtained from nitroanisole (0.2 mol), chloral hydraie
71
(0.1 mol.) and sulfuric acid (1-5 Mol) the compound
y1eld of ft~'v' and aemail amount. (5-A) 1,1,1-trichloro-2,2-~4-
mothoxy-3,-nitrophenyl)(21--methoxy-31-nitrophenyl)-etlittnt?. '111',
Card 1/2 With a smaller amount of Hoso (0A1 mol to 0.1 mol o-n-~tr'
4

.
.
MMM
=I
0

I
it
I
0
'
-

Condensation of o-Nitroanisole 'With Chloral Hydrate SOV/79-29-2-15/71
anloole) the authors succeeded ineeparating 6~6f of the inter-
mediate yrnduvt (1) (4-mothoxy-3-nitrophenyl trichlorc-methyl
carbinol). In 9ome condeneationa of o-nitroaniBole (0.2
with chloral hydrate (0.1 mol) and sulfuric acid (1 5 mol) only
-traceo formed of (1), while cempound (IV), meltInt; onl.~
3500, formed as the chief product. Ito oxidation 1~r--)ciu,,~
the positive rear.,tion on an anthraquinone nuclet,.s 'Pi,_t), ~-C':
to the paper* by Quelet (Ref 12) and collaborators 'Inc-
suppose the compound (IV) to be the pr!:~duct of autcconde%:~a_~;n
of (1) and to be a bi a- (mesotrithlorome thy!) -dime thoxy
dihydro anthracene (Scheme). There are 17 referenceo, I of which
are Soviet,
AMCIATION; Sredneaziatskiy goeudarstvennyy universitet- ((Soviet) Central
Asia"- State University)
SUBMITTEDt January 8, 1958
Card 2/2

YULDASW~ Kholut
Condensation of 3.--w=>-2-ml3tbyj-j-j)ropene and 1--r-blorg-l-but-ane
8;~ 160 IRA 3.4-- 1)
with benpene, Uzb. idLiz. 2i=. no.6*.,
1. Tashkentski.7 gosudaratvennyy urjvarojtqt im, V.,I, Lenim.
2. Chien-korrespondent AN UzSSR (for Tftkervanik)~
Cpropcme) (Batme) (Bmwno)

T.QUKERVAIIINy !*P. j , YULDASMp M% lus
Condensations of Tinf- halides --;itb t02uene and ammisole.
Zhur. ob. Mdm. 31 no.3:858-861 yz '61- (1-aRA 14:3
1. Tashkentskiy gosudaratvemyy universitet.
(VinylI ompounds)-. (Tolue-AD) (AnIsole)
c

YULDASHEV, Kh.Yu.; TSUKERVANY-X, I.P.
lczzm~
Reactions of thloroBtyrene with benzer-e. 72aw.ob.khim. 12 no.4i
1293-1296 Ap 162, (~9RA 15:4)
1. Tashkentskiy gosudarstvannyy universitet.
(Styrene) (Benzene)

ZWOV, 111m ftminovich, doktor ekoxiom.mauk;
istoricbesldkh nauk, red.; UMMOD, H.B., red.; BAMIYAROV,
M., tekbred.
[3conomic development of.Central ABia; from the second half of
19th century to the First World War) Ekonomicheakoe ra".vitie
Srednei Azli; so-vtoroi poloviny XIX stoletila do Wrvoi miro-
voi voiny. Tasbkont, Gos.isd-vo UzSSR, 1959. 295 p.
(MIRA 12:8)
(Soviet Central Isis-3conomic conditions)

MMGV~ A.K.; CSIINNA, E-'Xe-; Y=ASaN)
.Bit=n pc)t--i3tW Of ',L--50z0ia sed4-"--nts in Ust-Urt.
Uzb.geol;zl.iuro'- 6 no-2:38-45 162-

. - - -mr,4,L , --o
S- - - ---- NL - - -

FOGORZ 0~, J.P.a IULDASM
MAZSUDOV, N.Ml-
Artenivia scoparia.
Chemicai inveBt4gat
6 no.5.-84-86 16~. (MA 15-12)
Institut kbimii Tantiteltnykh veshchestv AN U,-,9SR.
MbaUstan-Art end sia)

Y-OLDASIEV., PXh-
YUM. ASIREV. P. "Investigation of the Alkaloids of Vinca erecta.11
Published by the Acad Sci Uzbek SSR. Acad Sci Utbek-
SSR. Inst of Chemistry. Tashkent. 1955.
(DISSMATION FOR M DEGIM, (IF O",TNIDIDA-7 TTI
CHEMICAL SGMICE),
So.: Kni-zhnaya letopisf
No. 27.7 July 2, 1955.

iL.
" PL
TErSUs()V, N.Yu,, akademik; yULD"H%V, Y.* IKWOVA. N.V.
Studv an Pl Ivids from the ahipvagrotmd portion of Vinca arecta
et Srh=alh. DAL AN Uz. SSR no.7:134i~ 156. WRA 12:6)
3..Akadgmiya nauk UzSSR (for Yunusov).
A
k
-`M

-t-he a,rtlf~
le "P-eserpin in P-r om a a erectz
imician of the Academy of Sciences Vvzbek SSQR and P. n. Yuldashev of the
.~-Institute of Cbezistry, Aeaaety of Sciences Usbeli SSR, m-att-U0,
isolation of the alka'oid.reserpicin fr= Vinca ere-.:t-a, a plant of the
Apocynaceae family closely related to tbe plant Rauvolfta. A total of 2.6~
.'Vercent of alkaloids are extracted W'Itb etber frm the roots of the plant..
These include the alkaloids vinkania--C,9H2~GN2, vinkadinin--C20H2403112,
AT)d reserpinin--C23HP604N2; reBerpinin 19 saponified with an alkali to
i-forn reserpinic acid. The acid and its nitrate are then methylated with,,
diazo=thaDe to obtaiiathe.,pare allmloid. (Doklady Akademii Nauk Uzbek-
9 - V9 r,
akoy SS% No - .561~ -pp-23-255Y

YUMOV, S.Yu. Tuldmhev, P.Kh.
Stud3r of the. alkaloids extracted from Vinca, eracta Rgl. et Sch-lb-,
Zhur.ob.khlu. 2? no.7.-201$-2018 J1 9574, (HlFd 10:10)
I.Imatitat,khinli Tastitolivkh veshchestv i khlop)m AN Thbekskoy
SSR.
(Alkaloids), (ApDanseeae)

- URAYE;V.,
study of allaloids Of Pedicularls RGL. ljzl,.Irhim.zhur. 7 no.3:
33-36 263* (Teuiu 1ID: 9)

YAGUDAYEV, M.R.; RASHES, Ya.V.; YULlD-hShDJ, P.M.
Infrared spectra of vinccaninp and its derivativen. Uzb. 'khir.
zhur. 7 no.6:54-58 163. (MIRA 170)
1. Institut kbimli rastltellnykh vesholnestv AN VzSSR.

DWASHEV., ~.Kh. I YUNUSOV, S. yu.
Vincarine, a new alkaloid from the roots of Vinca erecta RGGL. et
Dokl. AN SSSR 154 no.61l4l2-1413 F 164. (MIRA 27:2)
I. IPStitut khirdirastiteltny~ch veshchestv All UzSM. 2. Chlen-korrespon-
dent,:AN SSSR (for Yunusov).

- . n s t ~ - - I , K ~. 4 rr~:. i-,I ~ *, - , ~- , , --i? - -, .
- - , 1, - , - I -- ~-.
- 71' ,., - I . I - ,

U
f v _,rl I- a n 'I V i e -a A
165.
1. lns~~talv kh4-mli rasti t,---Ilr ves'-chestv All UzSSR. 2. Ch--,.,.-
korreDpor.-diento Uj' SSSR (for Yunuaa;,).

YULDASHIEIV~ PJl~; YUIIUSCV,, SOW.
Nrivatives of vinearWne, Uzb.kihin-ahur, 8 no.4:61-64 "J
(MIRA 18:12)
1. Institut khinii rastitelInykh vashobestv AN UzSSR. Submitted
December 20., 1963.

I
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cl,rom-oplinre aystem of
wt,!t-b IR conflrwied by the proiii2~!tlon af
hrqt'np, w"'.1) 2r-'$ by-Irochloric acid ylel~ied ea
tb,! lwlolemln~. base vitb zinc and vilfuric &c,-' 1~r, ehq
b:-~rohrilride in geid mediuu rlelded a
vhen reduced vlth godlilm luorfj~ry I i fj;-.-
pkntlwar, crtalyst occordlag to i"Amms in alcohn."
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XP6026897 SOURCE CODE: UR/C)062/65/000/012/215~-/-~'-~.~~
Ai7i'lliCV.: 75achenkova, M. A.* Yuldp.hev. P. tMusov, S. Yu.
CRG: lzistitute of the C em:-ft= ol'r"Wk~ e Matter. AN UzSSR (Institut FJrij-a'i
rastitellukh, veshchestv AN UzSSR)
-
LITLE: Vinervine -- a new alkaloid from the above ground portion of Vinca erecta
Rgi. eL-. Schm-alh
SOURCE: AN SSSR. Izvestiya.. Seriya~khimicheskaya, no. 12, 1965, 2152-2155
TOPIC TAGS: plant chemistry., alkaloidi phenol,~molecular structure,, melting point
ABSTRACT: Spocinens of the plant Vinca orecta, collected in Southern Uzbekistan,
were used for cold other extraction of.alkaloids, which were then divided into
phenolic and nonphenolic fract4ons. This romated in the subsequent isolation
of a now phenol base, vinorvine (%K
a~4172) (m-P- 154-15~PC) *Which is unstable
to light or Vaen in solution, and con s one OCH3 group and tvo active H
atoms one of which Is a phenole This now base caused a pronounced levorotation
of polarizod-3-ight, which points to the presence of a cluromophore of alpha.
nothylonoindoline connected to a calUmethoV3. group. Of the three oxygens
present in vinervins, one is a phenol bydroVl and two, are esters. Heating
vinervino In ansealoa and evacuated anpoule with 15% HC1 for 2-3 hr at 1000C
led to the formation of a crystalline indolordno base with a melting point of
18-5-1870C. which proved to be identicai to the indolerdne base obtained from
vinemidize (another, bAse present -Jm V, oraota), The Investigation of the
structuraII posiiion of the phenol hydYoxyl is continuing. 15PIgo- art* ha3;
1 figure. LJPRS: 36,455)
SUB COM, 07 /-SUBM DATE: 29Jul63 ORM REF-. 002 / OTH REF: 002
Card 1/1 UDG: 547.9

ACC NR: A?7011362
SMIRCE-CODEs UV0393/66/00/004/0293/0294
AUTHOR: Arlpovq 11. N.; Shaklrov,,T. T.; Yuldashev,. N.M.
ORG: 'Anstituto of Chemistry of Vegetable Mttorq Academy of Sciences USSR
(Institut khtmil rastitollnykh Teshchastv AN UzSSR)'
TITLE: Isolation of vincanino
SOURCE: Xhimlya prl rodnykh soyedinenlyg no. 49 1966, 293-294
XOPICITAGS.- plant-chemiStry, acatic.acid
SUB CODE: 07,06-
ABS TRACT: Vinconine was oxtracted by a countercurrent method from the roots of
Vince crecta Rgl..,et Schmalh-with a:-1 percentsolution of acetic acid. The extract
was desorbed with 1-5 Percent ammoniscal solution in 85 percent ethyl alcohol. The
condensed alcoholic so3ution-was aciWled.vith concentrated 'hydrochloric acid and
evaporated to remove alcohol, while the acid solution was alkalized with excess 30
percent caustic soda; and extracted three times with chloroform. The letter war,
dist-illed under vacuum to dryness and., af-ter.trestment with acetone vincenine was
isolated and converted into vineanine hydrpab~oride. &RSI 40,3~jl

YULDASHFV, S.
Effect of svace ar-.arigem-unt cn the forraticm of lcde~_-:r
5 tr,,Ic tureo c o r., ar, ljzt. biol. zhur. 81 no.".;-----
v A N' 7 -P;(V

(TLVZWMM) (KMAI M SO

YUIP~ASH~Vv- ..~4h.; ANCHURINAY n.A.
Role of carbDhydrateB in the lcdging of coA%-,+-on plants. Uzb.
biol. zhur. 7 no.6:67-73 163. (Y-EP-k 17-6)
1. Institut genatiki i fiziologii rastmiy All UzS-czR.

ymtmwt u) ~g. 7argam).
no rank Df progrannive vorkerD Is IncreaBimg. Prom. koop. 1,2 no.3:
6 Hr 158. (MMI 11 -3 )
1, Predsodutell pravleniya bblpromsoveta,
(7-sirgaus Province--Cooperative societies)

I
XULDASIM, U.I.
Vitamin 13-22 level of ths blood .9er= and zezw,- irm in ar-emiaa af
gastrointestinal -cfrigin. Probl. ~gmst. i peral. kravi 5
F 160. (Iau L~: ;-, ~
1. Iz kafedry propedevtild vnutrenni bolemey (zav. - Prof. 7.,-.
Atakhanov) pediatricheskogo i sardtarno-gigiyenicheskorrc fakul'+~--:
Tashkentsk.ogo mecU.tainsko 0 inst'Ltuta.
(CYAfTGCOBAL*fIm5 (IRON III THE BODY)
(ANVIIA)

"i-DASHa'? U.I.
Concentration of ~jitamin Bi2 and iron Ln b2ood samm in disea2es Cf
the liver. Med. zhur. Uzb. n0-3:20-12 Mr 160. (11!1,;~U 15:2)
1. Iz kafedry propedevtiki vnutrenni-kh bolezney (zav. prof. E.I.
Atakhanov) pediatrich qkng*-~-Atarnogo--i
0970 me s ko instituta
-(C owe .,)go_, (SMUM371IR011 IN THE BODY)
(L 1SEASIZ)

ATLMNOV 3 E. 1. 2 p7of .,* RLDASEEV
~, U.I., assistent
Amull.l. of vite=lm B19 and irom in bl*cd sa:-= in d-s-f-s-S.
Hod. zhuro Uzb. no*4-.8-13 Ap 161s (MIRA 3-4: 5)
1. Iz kafedry propedevtW vnutrenn-11 bole2ney p9dJatricheskago
i Banitarno-gigiyenicbeskogo fakulltetov Taahkentslcogo gosud-arstvenno;,7-n
meditsinskogo instituta.
(STMACH.-DISEASEES) (SERUIA) (IR0211 IN THE BODY)
(CYAN0G0BALAI=t

ATAIWIIOV, H.I.;UUUTIYJaIj A.M.; BUDD=, M.V.; 7ULDASEEV, u.i.;
SRAmSUTDINOVA, R.N.; YUMASBB7., X.Yu.
State of Boma metabolic indices in peptic ulcer of the sto-mch
and duodenum and the effect cgD them of hydrolysate therapy.
Terap.arkh. no.7:85-9-1 31 162. Omu, 15: 2)
I* Iz kafedry propedevtW vnutrennikh bolezney (zw,7. - chien-
korrespondent =1 SSBR i ALI Uzbekskoy SSR prof. E.I. Atakhancv)
pediatricheskago i sanita--no-gigi7enichaskogo falkulltetov TaBh-
kentsko o meditsinskogo instituta.
&-ymc mcm) (PROTEDI ODWLYSATES) (WITROGEII METILBOLISI!)

7UIDASHEV, U, I*
Dynamics of the vitamin B.12 and Iron content In the blood eqr=
in the pellagra syndrome. Terap. arkh. 34 no.5:71-76 '62.
(MIRA 15-- 6)
1. 1z Wedry propedevtild vnutrennikb bolezney, (zav. - chlen-
korrespondent AM SSSR I M UzSSR prof. B. L Atakhanov)
pedintricheakogo i sanitarnogo fakulltotov Tashkentskogo medi-
toinDkogo inotituta.
(PEUAGRA) (CYANOODBALARINE) (IRON IN THE BODY)
It

TUIPAS
3- kand.med.nmik
Contel)t of Vitamin B12 and iro in the blo od son= :in anemi,,.
7e-raP* arkh, 34 bo,32i69-74 D'6n2,, (14M .16:6)
-1- 12 kafedry propedertiki vnutrennikh boleznoy (zav.
11 - chlon-
Orrospondont JUIN SM i All UzSSR Prof. E.I.AtaMimlov) Podistri-
choskogo i sanita=o-gigiyenicheskogo fak-alt-.tcrv TlashkertskoCo
meditsinskogo instituta.
(CYAROCOBAIMMI (MON 17; THE BODY)

YULDASHENt Zh.
Char acteristics of-the petrographic composition of Mesozoic
Sediments -.Ln the northern Ustyurt. Uzb.geol.zhur. 8
no,3:34-38 164, (VIRA 16: 12)
-1. Institut goologii i razrabotld neftyanykh i gazovykb
zaestorozhd6niy GosudariAvennoto geologichesl-ogo komiteta
SSSR. Submitted Jan. 31, 1964,

r.ro:,;l Enct, On
3- 80 64
8 no
go. o T
7 m;t i tu i rinTabrAl-A rf-,ft.Yarli"'
c9c

ACCESSIONIM AT4042432 S/3103/64/000/002/0175/0182
AUTHOR- Usmanov, Eh. U., Tillayov, R. S., Musayevs U. N., Yuldasheva, Hh.
t
77TLE: Thermomechanical properties and plasticizing of grafted copDlymers obtained by
1: radiation polymerization
fizft
B07JRCE: AN UzSSR. Institut khimii polimerov. Khiraiya i -khimiya pfirodny*kh i
Jsintaticheskikh polimerov, no. 2,'104, 175-182
61 TOPIC TAGS: 9TRf" CopOlyiner, a-0'kylobitrl1e,-: polyvinylehlorlde, vinyl
I Polystyrene, '
perchlorlde, gliass temperature, GammR-irradiation, plasticizer, saponified copDlyrner,
radiation pDlymerization, pDlymer jdasticizing, polymer thermomechanical property
ABSTRACT: A study of the thermomeebanical properties of grafted copolymers obtained by
graftilng acrylonitrile on polystyrene, polyvinvyl chloride and vinyl parchloride showed that
the glass temperature To of these copolymers. regardleris.of the ratio of the compOnentS,
corresponds essentially to the glasB temperature of the initial polymers, but that the flo~v
temperature Tt lies above the temperature of chemical stability of the prodUctS. COPOlylnerS,
as compressed tablets (3-4 rnTn thick and 7 mm In diameter), were tested befDre and after
irradiation at doses of 1-10 Mr. The thermomechanical curves were Diotted with the
dynamcme~rlo soaloB of Kargin and Sogolova at u oowftant loadflor 10 sec., at a specific
Card 3

ACCE SSION NR: AT4042432
2
loadof 3..4kg/cm The curves obtained for all,the copolymers, with or without plasticizers
shoWed'JOSS
were quite similar, and effect of temperature than on pare polymers. Tabula-
ted Irradiation data showed that the.thermomechunical properties of grafted copolymers
remain almost unchanged under the influence of Irradiation. This indicates the greater
stability of grafted copolymers to )r -rays as well as to high temperatures. Theflowof
grafted copolymers IS therefore considered to be almost independent of grafting. Anin-
vestigation of the plasticizing of grafted copolymers showed that grafted copolymers syn-
I! thesized from two homopolymers which have a common plasticizer remain unchanged in
their compatibility with this plasticizer. For grafted copolymers containing, on the one
hand, chains able to plasticize (polystyrene, polyvinyl chloride) and, in the other component,
unplasticizable rigid chains {Wlyacrylonitrile), the compatibility with the plasticizer is low
and limited. The change in thermomechanical properties (decrease in Tc) with increasing
PLasticizer concentration (tetralin or methylbenzole ether) is plotted. In addition,
analytical data for nitrogen content and acid number of the grafted copolymers are tabu-
lated. The thermomechanical curves of saponified vinyl perchlorlds and pDlyacrylonitrile
grafted copolymers Bbo-wed that the glass temperature is decreased and the plasticity is
increased by saponification. A further Increasejn plasticity Is produced by plasticizers,
especially glycerol, Such an increaBe could never be obtained by plasticizing unsupDaified
d
rafte copolymers. Or1g. aTt. has: 2 UblOB and 3.figureB.
g
~.C ia".~
77
"MR7

In

~ ~ * , -. ~ ~ . 2"r- F. - - . ~ ~- - ~ -
F&f ed -ja Za F'- !"'I' ' `:' S ! -T~ ' ', K'-. -in- - a -I- :~ 7 ;-

7 -
Gatego-ry: USSR Physical Chemistry Electrochemistry B-12
Abs Jour: Referat Zhur-MAmiya) 9, 1957, 3 0 129
Author, Fhyzuiiin F. F-) Yuld asheva. L, X.
Inst Kazan' University
Title~ Study of Ancdic Behavior of zinc-- in.Alk.aline'Solutions
Orig Pub: Uch zap. Kazanskogo, un-ta, '1956- !-16) 110.5, 82-85
Abstract-. By the methcd of automatic recording of.the (CP t) curves
(Whim, 1957, 122,80) a stady was made of ano'aic polarization of
Zn- in, 0.25, 0.5 and- I N -.NaOH at 40 and 600 and I = 6 a/dm;'. Cn
application of the current the portential of Zn rises sharply and
evoluti,,;n of 0,, begins. C.-cidatisn Is attended by peric~iical, very
rapid, potential changes, caused by-periodical breakdcw-n ard forr-e-
ticn of oxide film. By the graviit~etric neithod a determination was
maie of the rate ofform-ation of oxide film on Zn at I of 6 and
12 a/dm'; an increase ofJ increases rate of formation of the film.
Cn-increase of the tenperature there takes place a decrease in
overvoltage of 0., evolution, which results in an increased rate
of formation of the oxidic film.
Card 1/1

8/048163/027/001/030/C)43
:Ef125/BIO2
:and Yuld
AUTHORS 3 Arbuzov, Bi, A4$, Samitbv, Yu.,
-proton magnet c.resonance-of the substituted dislo~
TITL'E% Spectra of
catione
-:PERIODICAL3 A"d Aya. nauk SSSR' Izvest -Seriya
A em -fizichaskaya, v. 27
M0.19 1963,~89_- 92
TEXT: A study c-if
the pn.r. Spectra of 2-methildiozolane, 2-chloromethyl-'
dioxolaneq and tTicbl6romet*ldioxoIame proved.tbat the influence of the
halide replacing the hydrogen in the metbyl radical of 2-methyl-1,3-dioxo-
-as far as.- the. protons of thelpethylene ~groups that are in
lane extends
-position with respect to tbe~'okygen, -'The' polar,: groups also cauco chemi-
cal shifts of tbap-hyd -rogenjq.#~_ Owing.-to the effect of the five-membered
rings the chemical shifts of the,protons in dioxalanie are by 0.3 smaller
than in the compounds witb open-chains (e.g. aviali orthoester). A sub-
stitution of the proton of--tb'v miethyl radical-by the first chlorine atom
influences the chemical shift*tAhp-prdbDrLa of the rbethylene group more strong-
ly than the subsequent introduption of further chlorine atoms. There is I'
Card 112

Card 2/2--d-

KATAYEVA, L. M.; ANCNIKOVA, I. V.; YULDASHEVA., L. K.-, K-ATkY'EV, Ve. C,
Reagtion of selemols vith ace-tylene derivstiv--F. Part 2
Stnicture of the prr-juctq of ipterartlon
3,; na. "e r
1. Kazanskiy gosudarstvenriyy universitat imeni V. 1. LTI_I-mnov--.-
lenina.
(Selenopbene) (Acetylene)

ARBUZOV.-J.3. A. ;
Dipole mownU and the confor=--tion of eye-lie c~:.=Fcumd-B. F~~p--:-I
1, 3-Di,.Ixo lanes a izv. AN SSSFL.Otd.khi=.nauk
1. "imichekiy inatiTut " A.M.Butlerova Kazanskogcr gasudarstvenn
uniyerviteta.
(Dioxolanep-Dipole moments)

ARBUZOV., B.A.; YULDASHEVA, L.K.
Dipole mameuts and the confor=tAon of cyr.21c m=pv=dv. 1z7.
Otd.khim.nauk no.20:173
.4-1737 0 162. 1
11 XhiTni skiy iwtitut-lia.- A.M.Btitlerov,4 Kazanskago gosudarstverLmgo
univorsitetao
(D;axane--DipDIe momenta)

ARBIJZOVp B. A,,- SMITOV, lu'. YU, I
~M ~=V~AL
P~O~ magnetic ra,00=08- spectra of, substituted dlaral=~m
IZV. AN SSSR. Ser. tit. 27 no.li89-92 JA,63.
(MIRA 16:1)
1. Xmz=IcI7 goaudarstvenMy universitet im. V. I.
*616ar wgn~tla raBonance and relaxation)
(DickLams,2pectra)

VAI 11.11
~XnBIBIW-11N,
star 6unts in the-dark Debulae Wing
Amal"Is of
116 no.1:89-92
Ogoroduikov (MMA IM5)
3..Xafedra astronomil.
(Nablulm) (Ogarodnikov, K-E-)

YULDASUTA, S.F.
SW,.v o; diffusion of endemic goiter in the veataxm dietricts
ontho Obu Valls7. Izv. AN Mx. SSR. biol. nauk 2 no. 6:73-77
160.. (CHU VALLBY--GOMR) OMIRA 14s 6)

YUIDAS13VA, S.N., kandidat meditainakikh nauk
Sanatorium sax-viess for mbsumatic child-ran in IT"ashkent. Pe-I iat-ri I-a
39 no.2.-43-47-Mr-Ap 156. (NL.Q-A 9:8)
1. iz niniki gospitalluoy pediatrii (dir. saBlu2henny7 deyatell
nauki vrof. R.S.Gershenovich) Tashkentakogo medit5iriO-r-go 1-11-
tuts Imeai Y.M.Molatova
twmmTI5m,-in Infaut aTd child,
marlageip U*t.. in sari htoritL (3~ap))

, ~:
j- I -

BUSSBLI, L.G.; YULDASHEVA, S.P.
Hamocultures of streptococci In caaes of rbc-matic fe-,-er tm
children. Ped-latriia 39 no*105-60 161.
1. Tz ka-f edry mikrobiologii (zav. Prof. P.F. Saamworov), kendrv
bolezney ukha, gorla i nosa (sav. --raf, 1-y-u.
noy pediatricheskoy klimiki (zav. 7of.
Tashkentskogo meditsinskogo Inatituta.
(MOURATIC MER) (STREPTIOCOCCUS)
E Ef

Decrease of r1wama-UC fever in S a-tl
in,
loefUlties of ii?,bakist" Trudy Tadzh. fae d
~1. Zaveduyushe-taya kafedroy faml e ts k
meditainskogo. Institutla.
tT

ima fever in c
hIdren in the Pn'al areas 0" Uzbekistan.
Sbor.nauch.trud.Tashrsmi ~2.~66-71 162.
m

IK~

7ULD -SIWA T.7u.
Effect,of overheatins and insolatIon on the blood picture
and raticulocyte conten-Vin the blood of bealthy and
decorticated dogs. Uzb. b1ol. zhur. 7 no.5:53-55 163.
Omu 18:11)
1. Tasbkentskiy gosudarstvennyy universitet imeni Lenina.

S/07 61/006/004/003/018
B121%2i6
AUTHORS: Sokolovao 11. D., Skuratov, S. 11., Shemonayeval A. M.
Yuldasheva, V. M.
TITLE: Determination of the standard enthalpy of formation of the
alpha and beta modification of metaboric acid
~.PZRIODICAL: Zhurnal neorganicheskoy khimii, v. 6, no. 4, 1961, 774-776
..TEXT: The standard enthalpies of formatimof the alpha and beta
modifications of metaboxic acid were obtained by detormining the standard
enthalpies of solution at 2950K. a-HIB02 was prepared by heating analytical
grade R BO for several days in an ampulla under a vacuum of 10-20 mm Hg
3 3
at 900C. P-HBO was obtained by heating boric acid in an open ampulla to
2
1600C- in the course:of-8 hr and keeping1t at.this temperature for several
..days- X-Ray-analytical dataimdicated the,products to-be the pure a- and
mo;ificationB. X-Ray analysis was made by A. A. Babad-Zakhryapin at
the Institut lizicheskoy khimii Akademii nauk SSSR (Institute of Physical

S/07e/6i/oo6/004/003/018
Determination of the standard B1211B216
Chemistry) Academy of Sciences USSR). The measurements were carried out
in a caloximeter with an adiabatic jacket. Metaboric acid was introduced
into the calorimeter in closed ampullas which were then broken. The
thermometer readings were correct to + 0-00050. The water equivalent of
the calorimeter was determined by electrical heating (" 171 cal/deg).
The temperature rise was 0-03-MVC for a-HBOV and 0.170C for P-HB 02'
alrpy
The enth of solution of a-HBO was measured to be 700 and 400 mole
2
H 0 for a final concentration of I mole H B031 both values agreeing
2 3
within the measuringerror. For P-HB02' the ent-nalpy of solution was
measured atLa'final concentration of I mole H BO to 500 mole H20. The
enthalDies of formation of the alpha and beta3mogifications of metaboric
acid determined at final concentrations of I mole H 3B0 3 to 500 mole H20
are. a-EB02 Aa H293 0.47 + 0.01 kcal/mole
P-HBO H
2 293 1.76 + 0.01 kcal/mole
The standard enthalpies of formation of the alpha and beta modifications
_CiTd_.

S/07 61/006/004/0/J3/0'8
Determination, of the standard'-... B121YB216
of metaboric acid from cryptalline boron and gaaeous oxygen and hydrogen
were calculated at a-EEO Ae. - -189.0 0,4 kcal/mole
2 formation +
P-EBO JXHO - -190.3 :t 0-4 kcal/mole
2 formation
..There are 2 tables and 10 references: 3 Soviet-bloc and 7 non-Soviet-
bloc.
ASSOCIATION; Moskovskiy gosudarstvennyy universitet im. M. V. Lomonosova,
Xhimicheskiy fakultet (Moscow State University imeni
M. V. Lomonosov, Chemical Division)
SUBMITTED: March 4,-1960
Card 3/3

n. 5t9j. 4M 4;
he ptL -yelas 54.
It - Cinn ww Tnth thm "aw ior
an intuscLica bCSHV, 06 tile 2 aft
01 AD 3 4r Ow xxu
VOO b- dMided In j&;jOj of, 1 s,2 VI the
Zltm
vim by ex age
cum cm the the I n Ron.
~e of
Os 31,71. d
nkae 1; t aht.
Tbe. saw Ua no
the
A wo,
OBa), b, 111-17' 4 1.41
0 . 0.9749,'
C411u)s h. 172.5-2 - 0 -_ 11 MC.
fOCsffn)jbj42D7-8A. 1 28' 27 p . El C.
IL ~ A .7

YULIKOV) H. I
1949)
R,ev. st--nki i inf;tr=ent,

yullrKo."ll lK.I.
I . ;,:
: ~- --1. .
I , 7 4 - ~-` .
p,- - ---

-M

SEMENCHENKO, D.I., kand. tekhn. nauk; SHEVCBENKO, A.N.;jULIKQ.V,
M.1 kand. Ukhn. nauk-p na=hnyy red.; CHIGAREVA, E.I.,
red.; VIMROVA, Z.B.y tekbn. red.

I
i
i
a
I
I
i

,. -.. ~
.'- , j.1, - !
. , 11 :~ ~~ ;,:: w i,-'.

KHOXHLOV, A.B.; SIIAMy SUPANOY, V.M.; YULIKffA-, Ya, .; TRWHKO, Ye,V.;
LEVIN, Ye.D.3 YMMWE, S.M.; SINITSYNA, Z.T.; CHI CHAN-TsIll LGhlil
Cniang-Chling]; SOWVIMA, N.H.; lVINSKAYA, S.A.; ROSSWSKA~!- 7'
JNITRIUVA, V.S.; MMOV, S.M.; Mllsl R.A.; BEP,:-,Zlra, Y.3..;~,;
MMOVA, LaKe
A -nev t7ps of pol~nyxln) polyzyxin 14. Antiblotiki 5 no. 1: 3-9 Ja-F
60* (141M 13:7)
bigtitut antibiotikov i
laboratorip Icbimii belka i antibiotikov khimmicheskogo fakullteta
-MOskov - -kog oor-dena-Lenima gasudarstvew-c"go M.I.T.
LomonoBova.
(POMMIN)

ircir.
of PolrAxan 141 tivation.-If
Report presented At Vie 5Vi 'Internatinnal Biocmmistry Cona,,ress,
Moscow 10-16 August 1961

11
SILAUV A.Be.- STEPANS VA~-4-IDUKO
A
YO.P. k JOiWVA
G
L
,
-
.
.
.
-
..

'Cb8mistX7 Of P027mixin M, Part 2-- Quantlu 4'
tJTA--4;anO acid cr7--~-
position. Zhur. ob. Vhlm. no.3:1023-1026 kir f61. (MA 14:3)
2, Moskbv skiy go-sudarstvannyy ur dver4tet.,

ARM
LN

I , Ye.F.; MURATOVA, G.L.
SIUM A.B.; SUPOOV V.14. Y~,L ~KOVA~
Chemistry of M. Part 3: Partia2 h-wdrol-.,zir, ol'

IA, I
YU,LIKD-VAYS.P.; HICHWIV -yu-
(Bb2gari7a); UDAIVIAIT&-4--~~

SILAYEV, A.B.; YUUKOVA_, Yp.Po; BARATOVA, L.A.
x - Identification of fatty acid.
Chanistry orpolynyxb H~ Part 5:
Zhurobkhim, ~32 ~no,341"20, Fz 162. (MRA 15:3)
1. Moskovskiy gosudarstvennyy universiUt imni H.V.Lomonosova.
-(PolynyxinB) (Acids, Fatty',

XONOSHENKO, I, - jl"- ~

VOW-EPSETEM, A. B-; GR'GORSYEVI S' ""; -KRICMO, A. A.; KMIYASHINA,
R. A.; SUR07-PSEVA, V. V.; YULYJ M. K.
Pjroductlvn of aromatir. bydrocarbDne--from pyrolysis tar of b3rdro-
caTcon gases by hydrogenation, Trudy IGI 17:269-277 162.
(141RA 15: 3-0)
(Ilydrocarbons) (Coal-tar products)

t-EPSHTEYN, A.B.; DAIMAN, N.A.; LISYUTIKINA, L.N.
InvestIgating t1h, co"-positio-11 of the pmducta of the a3
phenol with i9obutyl alcolhol and isobutene. Naftakhimiia 4 no.5:717-
72-1 S-0 164. (MIRA 18:1)
1. Institut goryuchikh iskopayem3rkh All SSSR.

ir
~1~ 4 1
kC=, 5-:10104 VR! AY5015hPM
p,; ftsa~,c7.
T i r -Z, A metbcd for 'be preparation of P~-
izdureteni, i '-o,--&rnykY,
r5
,:c yj r ~3 t y I DI e n1 s e
'AKT'RACT! The prppaxatlon of p -t. e rt -1-,,.rt y I~phen n v
Jmd tr.'-'Ver4,-*riitylp~-iu-nol,-, In tha pre-.~~mee of' 6v-- a,-