SCIENTIFIC ABSTRACT ORLOVA, T.I. - ORLOVA, V.M.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001238230005-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 3, 2017
• Document Release Date: June 21, 2000
• Sequence Number: 5
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

OfakVAj . I t_-.
L
Molding and aoro m!xt,,Lr-,m wttfa Iluoi ai buiJoir.
1-4, no.7tlc,4.-20 Ibl.

oHLOV.Ap T. .1.
11 lnvestiga~im of ujo Speed cf Motion of Metals Aloy,g ",old
Canals." Cand Tach Sci, '~!Oscow I-st of Nonferrous Metals and
Gold imerii 14. 1. ialinin, Min. -iir~her ',ducation 7~'SSR, '-Ioscow, 1?54.
(KLY '4o 7, Feb 55)
3 -1: SUn. 'To. 631, 26 Aug 55-S-,xrv~-v of Scie,,Aific and 'i'er-h-)ical
Disserl'a-,io:,s i~efended at U-53k H-gher -;ciurational

mvnr-

e

Omom~ T. I.
"Research on tne Velocity of Flow of Metal Through the Conduits a Castin~,, Mold."
Hydrodynamics of Molten Metals (Gidroiina--,ika rasplavlezinykh metalon~; D, ri .:,
saveshchaniia po teorii. liteinykh protsessov. Moskva, Izd-vo Akad. naur 38SR,
257 pp.
(Proceedings of the First Conference L)n the The,iry of Casting Prucvsses)
"M. I. Kalinin" Moscow Institute of Nonferrous Metals and Gold

*A, 7 _7
~;;O.I Orlov,-,, Canl-idi:~e ci .7echnical -;,cic-nceq 128-56-4-1,7/1e
-Si Alloys (Modifitsirow-niye
Lodification uf Icat-Resistant Al
zharoi,roc?inyk.-. 3,1---fov na osnove AI-Si)
k zalCuj I CAILz Liteynoye 1,rod-,vocotvo, 1953, -10. 4, pp 31-32 (Uzi~iR)
,,BI-)2iLACTI This iz En sbatrhct, or translation, of a french-i&n.-ur-~~7c
axticle publishcC in "'Fondurie", No. 141, 1957.
.1
'here ire i fizuroz. and 12 nor.-Soviet refc-rences.
,',VAIA'--:.BL:;; Library of ',;on-
1/1 1. Heat resistant alloys-Kodification

18(5)
snv/1 28-5Q-5-31/35
AUTHOR: Orlova, T.I., CandidAte of Technical Sciences
TITLE: Novelties in Pressure Die Casting
PERIODICAL: T-iteynoye Proizvodstvo, 1()5Q, Nr 5, pp 43 -Ar) ('-R)
ABSTRACT: A summary of articles from The ~Ietal Industry, Nr 2
and TTr 15 and Revue de l'Aluminium Nrs 252, !Tr 21~5
is given here.
Card 1/1

ORIOVA, T.I.
Production of alloys for the manufacture of pistons in Went
German.v. Lit.proizv. no.2:47 F '60. (141RA I !: ,
(Germany, West-AlumInum alloys)

ORWYA. T. I.
Present day expamlon of the casting In tbs, United States. Idt.
prolsve no.11:42-47 N 160. (MIRA 13:42-47
(United St"em-Die castizg)

BARZIY, VA. , inzb.; IOFFE, M.M. , inzh.; CHERKASHINA, N.P.. insh.1
ORIDVA., T. 1. , inzh.
Incraming the corrosion resistance of electrically welded
Ml8N9T steel pipe. Stall 22 no.10:9" 0162. (MIRA 15:10)
1. Zaporozhskiy staleplavillnyy zavod.
(Pipe, Steel-Corrosion)

7.
ORMA, Tel.; "VRIWT. N.I.
Ilectro-reduction as a method of protein investigation. Plart 1: Study
of cor4mmts, formed during electro-reduction of some dlkotopipera-
sliwa. Shur. ob. khlis. 27 no.12:3314-3321 D '57. (MIRA 1113)
1. NDniwvskly gosudarstvenny7 universitat.
(Reduction. Ilectrolytic) (Piperaztne)

ORLOVA, T.I., Cand Chem Lici -- (disz;) "Elect, -*ca.! reducti(,r) f
di4etopiperazin Oiall-ila_ides of a..,iro acids, pe.-tideb
of proline, -.nd C grami-cydine." Vos, 1959, 15 p1- ("os ~~tz,,Le
Univ. UheaAwUW caculty) IOU copies (YL, 34-r~9, 111)
- 20 -

AUTHORS: Orlova, T. I., and Gavrilov, N. 1. 20-2-21/50
TITLE: On Some Electroreduction Products of Gramicidin C
(0 nekotorykh produktakh c-lektrovosstanovleniya
gra-mitsidina C).
PERIODICAL: Doklady AN SSSR, 1957, Vol. 116, Nr 2, pp. 239-240 (USSR)
ABSTRACT: The conception of the existence of a d,keto-piperazine cycle
(consisting of proline and phenylalanine) in Cramicidin C
was obtained on an indirect way. Namely based on the
reduction of amino-nitroCen by 2 &mine Croups in the
hydrolysate of the reduced t.-ramicidin C, compared to the
hydrolysate of a non-reduced rramicidin C. The au,hore
considered it important to isolate 1,2-trimethylene-5-benzyl-
piperazine, which comes from d-phenylalanine-l-prolyl-
anhydride, from the reduction products. In spite of the
reduction of 1 g t,ramicidin C it was not possible to discover
the piperazine souCht for. The authors isolated the basis
which proved to be d-phenyl-alaninol (a-benzyl- a-amino-
ethanol).
Gavrilov and Koperina observed the reducibility of the
linear dialkylamides of plivnyl acetic acid, but did not
Card 1/2 thoroughly study the reaction producls. The authors for the

On Some Electroreduction froducts of Gramicidin C 20-2-21/50
time being refrain from dealin,,, with the causes of the
formation of' an amino-alcohol in 'he electroreduction of
t-ramicidin C; this apparently is the chief direction of
the reaction, as Ihenylalanine completely disappears,
whereas d-phenylalanonol was alone determined from the
number of the reduction 'iroducts. An experimental Part with
the usual data follows. There are 7 references, 2 of which are
Slavic
ASSOCIATION: Moscow State University imeni M. V. LomonOBOV
(Moskovskiy L~osudarsl.vennyy universilet im. 1. V. Lomonosova)
PRESENTED: By A. F. Nesmeyanov, Academician, May 7, 1957.
SUBMITTED: May 4, 1957
AVAILABLE: Library of Con;ress.
Card 2/2

SIlAYKV, A.B.;_ORLUVA, T.I..; KUZNETSOVA, V.S.; MIRONOVA, I.B.
Ghemical characteristics of aurantin. Antibiotiki 5 no.3:19-Z
M76-Jo 160. (MIRA 14W
1. laboratoriya antibiotikov biologo-poohvennogo fakullteta
Moskovskogo gosudmeptvannogo mlversiteta.
(ANTIBIOTICS)

SIUYEV, A.B.; KUVIETSOVA, V.S.; ORLOVA, T.I.,- MIRONOVA, I.B.
Amino acid composition of aurantin fractions. Antibiotiki 6 no.l:
25-29 Ja 161. (MIRA 14:5)
1. Laboratoriya antibiotikov biololp-pochvemogo fakullteta Moskov-
skogo gosudaretvennogo uaiversiteta.
(ANTIBIOTICS) (AMINO ACIDS)

SIIAYEV, A.B.; MIROINOVA, I.B.; CHLOVAp T.I.; RINETSOVA, V.S.
Chmdeal structure of the 44fraction of aurantin. Antibictiki
6 no.7-.597-603 Jl 161. (MMA 15:6)
1. Laboratoriya antibiotikov biologo-pochvennogo fakullteta
Moakovskogo wiiversiteta.
(ANTIBIOTICS)

XUALRETSOVA, V.S.; MIJWN0VA, I.B.; QRWVA, T.I.; SIIAYEV, A.B.
Chemical structure of tho componento of the antibiotic
aurantin A2 and A3. Antibiotiki 7Vno.3230-34 Mr 162.
(MIRA 15;3~
1. Laboratoriya antibiotikov biologo-pochvemogo f&kullteta
Moskovskogo ordena Lenina universiteta imni Lomonosova.
(ANTIBIOTICS)

SHAPOSHNIKOV, V. N., akadmik; NKrZWVA, M. V.; ORLOVA T. I.-
Ij -
MIRDNOVA, 1. B.; MrZNMOVA, V. S.; Zuton,--r- V.;
SIIAYXV, A. B.
Formation of now fftctions of auranthin and the study of their
chemical and biological properties. Ddkl. AN SSSR 147 no.6.*
1476-1479 D 162. (141 RA 16 t 1)
(Auranthin)

SHAIWHNIXOV, V. N. ; SILAYEV, A. B. ; NEFEWVA, M. V. ; ORLOVA, T. I. ; KUZUETSOVA, V. S. ;
MIRONOVA, I. B.; ZUBOVA, 0. V.
"Directed biosynthesis of aurantin and investigation of biologicai and chemic&~
properties of new aurantin fractions."
report submitted for Antibiotics Cong, Prague, 15-19 jun 64.
Lab of Antibiotics, Faculty of Soil Biology, Moscow State Univ.

SHAPOSHNIKOV, V.N.; NEFELOVA, M.V.; ORLOV1,2.1-~ .511AYEV, A.B.
Effect Of levomyeetin on the development and antibiotic-formati=
activity in organisms producing aurantin. Antiblotiki 10 no.1:13-18
Ja 165. (MIRA l8r4',
1. Biojogo-poe~hvennyy fakulltet Moskovskogo universiteta imen!
Lomonosova.

at
W. QQ 11, 7-ib
1", Ow"
~titir roe Ma
jot
I - 4~
rod $us
*W* WON,
A, .1
p,
1

ORWVA, T. L FD 193
USSR/Chemistry - Dyestuff Intermediates
Cara i/l
Authurs Orlova, T. I., Luyashevi--n, V
Title Reactions whi,-h -ompli a: e Lhe syntf.esis ~,f a~_etuace'~'_, a. i,;
arylaraides
Periodical Khim. prom. 4, 21-~~ (21'---17). -June 1)1,)4
Abstract Describes a detailed inves--ibation of the preparation of acetoacet-c
acid ar)lamides under various ~oriditions with the aim of findin6 the
best procedure for Industrial application. Established Lhat while
the enol content has no influence on the yield, even traces of acid
are harmful, because they expedite the formation of ethyl crotonate.
Recommends addition of' nuri-volatAie and rion-ieactir)6 urh;anic Dases to
yl a,cnlon-etate and arylamine One USSh ref-

AUTHORS: Orlova, T. I., Gavrilov, N. 1. 79-12-27,%3
TITLE.' The Electric Reduction as a Method of the Investigation of
(Elektro-vostanovleniye kak metod issledovaniya belka).
I. The Investigation of the Compounds Forming With the ~_lectric Re-
duction of Some Diketopiperazine (I. Izueheniye veshche-stv, ~~cjazuy-
ushchikhsya pr-- e1ekbrvNos3tanovler_ii nekotorykh diketopiperaz_liov).
PERIODICAL: Zhurnal Obshchey Kh1mii, 1957, Vol. 27, Nr 12, pp. 33"_3~21
(USSR).
ABSTRACT; Following earlier works the authors continued the investigation of
the electric reduction of diketopiperazines at the mercury catriode
and by means of the chromatographic method on paper investig3ted as
detailed as possible the compounds forming in this case. At '-he same
time piperazines were separated and their structure was prov,-". The
chromatogram, in relation to the electric reduction of the glycine=
anhydride (figure 1) shows that the cathode solution contains very
little glycylglycine, glycineanhydride and possibly glycine during
the reduction of piperazine after from 3 to 6 hours. Also chromato-
graphically shown was that after the reduction of diketopiperazine
the hydrolysetes of the cathode solutions contain the respective ami-
Gard l/ 2 no acids and piperazines but no other products. The electric reduc=

The Electric Reduction as a Method of the Investigation of Albumen. 79-12-27/43
I. The Investigation of the Compounds Forming With the Electric iteddlaztIon of 5,r,=e
Diketopiperamine.
tion at the mercury cathode was investigated with the following dikew
topiperamineB: glycine-anhydride, alanineanhydride, glycylalaninean-
hydride and glycylphenylalanineanhydride. Thus the authors showed
that piperazinea form with the electric reduction. Their structure
waa proved by the production of their picrates and dinitrophenylde-
rivatives as well as by means of a comparison of their characteriss
tics with those of the corresponding derivatives of the know pipera-
zines. The synthesis of the piperazines does not take place with prq-
liminary formation of aminoaldehydes. A system of solvents for '.he
chromatographic classification of piperazines was proposed.
There are 5 figures, and 16 references, 5 of which are Slavic.
ASSOCIATION.' Moscor State University (Moskovskiy gosudarstvennyy universitet).
SUBMITTED: Novemoer 3op 1956.
AVAILABLE'. Library of Gongress.
1. Crganic compounds - Chromatographic analysis
Card 2/2 2. Diketopiperazine - Electric reduction

67 758
IS7 0
i_i+~r~~ S/064/59/000/07/006/035
AUTHORS: grlova, T. I., Candidate of B005/B123
Makarovokayap G. M.
1~
TITLE: Synthesis of Some Azo Pigment Dyes for the Varnish Industry
PERIODICAL: Khimiche8kaya promyshlennostlt 1959, Nr 7p pp 582 - 584 (USSR)
ABSTRACT: The present paper describes the synthesis of red azo dyes. The
authors first synthesized two azo pigment dyes that are used as
car varnish by various firms abroad. The qualities of these pig-
ment dyes, the composition of which is given, however, were not t1-1
very satisfactory. In order to obtain light-fast and opaque
azino and diazo pigment dyes, the authors investigated aromatic
amines of the general formula: Y xx NR2
( I
X X
X - -C1, -H, -N02, -S02N-----RR -CONER2i R, R1, R21 - -H, alkyl or
aryl residues (the latter may contain an amino group and one of
the following subatituento in o-position: -CI, -CH31 -OCE3 et al.)
Card 1/4 Y - -CH3, -OCH 3' _OC2H5' _C6H5 etc.

67718
Synthesis of Some Azo Pigment Dyes for the Varnish SA 4/59/000/07/"008//035
Industry B005/B123
Various arylides of the 2-hydroxy-3-naphthoic acid were used as
azo component. Developing was done in an aqueous-alcoholic
medium, or in an aqueous solution with an addition of 10-12~ of
ethylene glycol or Cellosolve at pH 4-5-7-5. Only in a few cases
developing was possible in acetic acid solution while using
auxiliary agents (preparation OS-20, emulsifier of the type IN,
Igepon T, and others). The use of ethylene glycol and Cello-
solve is especially recommendable for a synthesis of diazo pig-
ment dyes. Of the synthesized pigment dyes, the dye from
3-nitro-4 amino anisole and 5'-chlorine-21, 4'-dimethoxyanilide
of 2-hydroxy-3-naphthoic acid should be mentioned. The quali-
ties of this pigment dye car, be essentially improved if the
synthesis is carried out with an addition of 5-1(y/o' of manganese
pigment of the azo dye from 5-nitro-2-amino anisole and 2-hy-
droxy-3-naphthoic acid. For varnish coats ono pigment is of
great interest, that is obtained from 3-nitro-4-amino toluene
and the o-anisidide of 2-hydroxy-3-naphthoic acid. This pigment
dye is found in two modifications: dark red with a bluish tinge
Card 2/4 (unstable) and bright red with a yellowish tinge (stable). The

67 'q8
Synthesis of Zome Azu D;,ec, fcr tle Varnish 9/06 59/000/07/008/035
Industry B005YBI 23
Card 3/4
transition from the first into the second form occurs readily by
the drying process of the huraid dye at 60-700, or by treating it
with various organic solvents at room temperature. The stable
form is very fast to light and has good covering power and tem-
perature stability. The stability to various organic solvents is
specified. Some others of the synthesized pigment dyes coagulate
nitrocellulose and therefore cannot be used as nitro varnish.
Among the synthesized diazo pigment dyes the following ones are
of interest: N C ~_ x N
Y YJ
N
H HO!~O
CONH-