SCIENTIFIC ABSTRACT YUDANOVA, L. S. - YUDAYEV, N. A.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001963030006-3
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 99
• Document Creation Date: November 2, 2016
• Document Release Date: September 17, 2001
• Sequence Number: 6
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

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SHVARTSY L. Si,, prof.; LOBANOV, V. ff.-.LEBEDEVA, Z
.-Changes of-the myoWdium in Botkinlo dioease. Terap. arkh.' no.9:
71-78- 161. (MIRA 15.2)
1. Iz kaf~cb*y gospitallnoy terapii (zav. prof. L. S. Shvarts)
lachabnogo fakullteta Saratovokogo maditsinakogo instituta.
(HEPATITIS, INFECTIONS) (HEART-DISEASES)

sMT A R---'S L.S.; SIIUB, G.M.; YUDPINQVAY L.S.
Timinollo-gy- of atherosclerosis; prelirdr-fry rf"prirt.
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ACC-NKt AV6029 21, So= UR/-0413-/6-6-/-000/'Di4/0058/0058'-I
INVLNTOR: Fedorov, V. N
Yudashkin, A. G.
ORG: none
TITLE, Slot-type gas burner. Class 24, No. 183871
SOURCE: Izobret prom obraz tov zn, no. 14, 1966, 56
TOPIC TAGS: gas:,burner, gas combustion
'ABSTRACT: The proposed gas burner contains perforated pipes for the as supply which
are located above a longitudinal exit slot of an air duct. In order to ensure a con-
Fig. 1. Gas burner
gj~- -44 Perforated tubes; 2 enit sli
air duct; 4 guide vanes.
I Card 112 AD-CL-66. .951.2

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r-C-C ~~R% AP6029042
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excess of air supply along the whole length of the burner$ the.ratio of the
slot area to the area of the air duct cross section is equal to the ratio of the
total aperture area in the perforated tubes to the area of the cross i5ection of the
tubes. Guide-vanes-are placed in the exit slot of the air-duct; perpendicular to its
longitudinal axis (see Fig. 1). Orig. art.,has: I figure. [AV]
SUB CODE: 21/ SUBM DATE: 14Feb64/
L_j~ard _-2/2

Test equipment, has been introduced, -Radio, no&6:13 A '63;,,
(mm 16:7)
1, lqachallnik radipkluba DobrovollnogO ObshchGstla oodayst
arajig aviatoii L flotut GOmOl Be ~ - I I I .
(Mao --- Equipment and supplies)

YUDMKMI M* No
UM/Ehysics Dielectric Strength of Paper Jan 52
"Dielectric Strength of Condenser ftper-in,a Compressed-Gas-Kediua.0 T. T& Rome, 9. H.~
M. H. Yudashkina Leningrad Fbys-Tech Inst,, Acad'Sci -USM. a2hur Tekh Fiz"
Reynov,
Vol XXII., No. 1. pp 1640
Investigates the depen dance of ruptwe strength E (in kw/mm) of condenser paper upon the
pressure of gas (elegas, nitrogen, etc. In Wsq cm) for various thicImeesee of paper and
-make.- Concludes that-the use of paper can be expeditiously recommended'in dielec techno-
logy. Submitted 5ApAl 51
A. 206T99

AUTHOR: Yudasin, L. SOV-4-58-10-4/39
TITLE; The Yomeomol Millions (Komsomollakiy million)
PERIODICAL: Znaniye - sila, 1958, Ur 10, PP 4 - 7 (USSR)
ABSTRACT: The author describes how the suggestions of three innovators
of the Klin Trust of Artificial Fibers brought about savingS
of 1,000,000 rubles a year. There are 8 photos.
ASSOCIATION: Klinskiy Kombinat Iskusstvennogo V-olokna (Klin Trust of
Artificial Fibers)
Card 1/1

ILI
r-,. YUDASI#, Dev.,
Tractor operator-leaves the cabIn. Znan.stia 34 no.2:14-16 F 159.
OURA 120)
(Tractors) (Ramote control)

YUMSINI LOT
Fertility cachins-. Znan.sila 35 no.1:8-11 Ja 160.
I:MR& 13:5)
(Agricultural machinery--Technological innol.rations)

-YUDASIN Lev
n9 fWM A ~l

TMASR, A. U,
Berazovskaya, F. 1. and Yuclasina, A, G. -tIThe effect of a-'solvent on the kinetics
of-or:yanic peroxide deco:;pcsition,"Nauch. zapiski kDneprcpetr. gos. im-t), Vol.
XMI1,1946, p. 85-93, -Bibliog: 18 itemz
SO: U-521w, 17, Dec. 53, (Letopis tZhurnal Inykh Statey, No. 25, 1949)-

BKRZOVSK&TA, F. I. .(deceased]; SEAM. O.K*; !PMSEDMICH, R.O..- TW)ASIMAA.G
Stud7 of the mobility of hydrogen atoms in salts of dibasic acids*
Ultr.khim.zhur. 24 no.6.-741-745 58. (MIRA 22t3)
1. -Dnepropetroveki7 gosudars.tvepr07 universitat.
(Acids, Organic) (H7drogen)

rAYA. F.I. .(deceased]; SKAM. O.K.; TROMMICHo HoO.;
Study of the mobIlity of the hydrogen atom In d1basle carbO3711C
acids. UkrAhim.zhur..25 no.lt45-49 159. (KRA 12:4)
1. Dnepropetrovskiy gosu" rstvamW universitst.
(Acids, Organic) (Elydrogen)

5(3) SOV/79-29-6-211/72
AUTHORS; --Malinovskiy, Yadauina, A. G.
TITLE: Investigation in the Field of Unsymmetrical a-Oxides (19s1edova__
niye v oblasti nesimmetrichnykh a-okisey). Synthesis and Pro-
perties of tnsymmetrical. Oxides of Mlethyl-isopropyl- and Kethyl-
tertiary-butylethylene (Polucheniye i avoystva nesimmetrichnykh
okisey metilizopropil- i metil-tret.-butiletilena)
PERIODICAL: Zhurnal obshchey khimii, 1959, fol 29, Nr 6,
-pp 1689 - 1892 (USSR)-
ABSTRACT;-- This paper'&eals vii-th-the capability of the unsymmetrical
a-oxides of hydration- andisomerization reactions and of oxy-
amine formation. A number of authors (Ref 1) have found that the
hydration of the a-oxides of the aliphatic series with a tertiary
carbon atom in the oxide rinG proceeds very vigorously, In the
investigation of the a-oxides of methyl-isopropyl-(I) and methyl-
tertiary-butyl ethylene (II) it was found teat they are iso-
merized reae-ily to form the aldehyde, even on heating or distilla-
tiong but that their hydration is difficult.
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Investigati on in the Field of Unsymumetrical a-Uxidan. S07/751-29-6-25/72
Synthesis and Properties of.Unsymmetrical Oxides of Methyl-isopropyl- and
'Methyl-tertiary-butylethylene
(CH H~ (CH ) C C CH
3)2q 3 3
H C 1, 3C 0'~~ 2
3
The principal hyd*ration products of these oxides are their
isoners, the aldehydes, what was also observed by Pansevich-
Kolyada (Refs 2,3). The considerable tendency of the unsymmetri-
cal a-oxides of the olefins towards isomerization wan described
by many authors (Ref 4). On the basis of their experiment al
data and of those published, the authors assumed that the pre--
sence of a large number of nucleophilic substituents polarizes
the oxide molecule in such a way that its Most hjdrogenated
carbon atom becomes more positive, whereby the migration of the
hydrogen atom to the neighboring carbon atom which has a large
electron plane,-is facilitated. In this connection the oxide
of compound (H) is of special interest. With ito synthesis
already a large number of polymers is formed, wl~iat causes a
smallyield in the oxide. The reaction of the oxide with diethyl
Card 2/3 amine mainly also yields polymers. From the oxide of compound

Investigation in the Field of Uneyauetrical a-Oxides. SOV/79-29-6-25/72
Synthesis and Properties of Unsymmetrical Oxides, of Methyl-isopropyl- and
Methyl--t4rti,ary-butyle-thylene-
(I) the oxy-amine is formed in good yield. On its isomerization
also glycol is formed in addition to the aldehyde., Compound M
has also nucleophilic radicals but less than (II),, On the
attemp.t to obtain compound (II) by oxidation of the correspond-
ing unsaturated hydrocarbon with benzoyl-hydro-peroxide the
authors instead of the oxide the monobenzoate of glycol (III)
or (IV) (Scheme 2). Formula (III) is the more probable one
(formation of iodoforLa). The formation of the monobenzoate
could be explained according to schem4 3. There are 13 refer-
ences, 8 of which are Soviet.
ASSOCIATION: Dnepropetrovskiy gosudarstyennyy universitet (Dnepropetrovsk
State University)
SUBMITTEDs May 2o, 1958
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S/079/60/030/00~/018/033/xx
5,.7"400 1-~Zl BOO,1/BO55
AUTHORS3 and Yudasina, A, G~
- ----------I--------------
-
TITLE-. Studies on Unsymmetrical o~-Oxides. I!. Synthesis and
Properties of the Oxides of Methyl-phenyl-ethylene,
Ethyl-phonyl-ethylene, Me'thyl-o-tolyl.-ethylene, Methyl-
benzyl-ethylene, and Methyl-cyclohexyl-ethylere
PERIODICAL: Zhurnal-O-bshchey khimii, 1960, Vol,, 30, No. 6,_ pp. 1831-1837
'
l
ethylene oxidesi
were prepared by treating
TEXTt- Unsymmetrical initial
chlorohydrine with alkali bas . Many researchers kRef._2) found that
and unsymmetrically disubstitut4d-ethylene oxides -
,
generally isomerize to aldehydes. This isomerization readily occurs with
aliphatic radicals. It is also known t .hat monosubstituted *(-oxides of
are diffioult to isomerize. Experiments
the type C H (CH ) CH
2
6 5 2 p
0
barried out by the authors of the present work confirmed this rule.. Thus,
of all the -J,,-oxides discussed in the present publication, benzyl-methyl-
ethylene oxide is least easily isomerized, yielding a mixture of
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85390
Studies on Unsymmetrical c C6H By
3. 6 4 > 6 11 5 > C6H5Cff 2-
treat'ing the corresponding chlorohydrins with alkali-hydroxide solutions,
the authors obtained unsymmetrical o(--oxides of melphyl-phenyl-ethylene,
Card 2/4

- ----------
8 ~016~
Studles on Uns -trical --/-Orides, IL, S/079/60/030/006/018/033/XX
YMM
Synthesis and Properties of the Oxides of. BOOI/BO55
Metthyl-phenyl--ethylene4 Ethyl-phenyl-ethylene,
Methyl-o-tolyl-ethylene,.Methyl-benzyl-ethylene,
and M~41-hyl-cyclohexyl-ethylene
ethyl-phenyi-ethylene, methyl-p-tolyl-ethylene, methyl-benzyl-ethylene,
and methyl-eyelohexyl-ethylene (Ref. 1). So far, the last four have not
been desoribed in publications., The oxides were hydrated under different
conditions, in'the presence of HCl or H 2s0 4.. The oxides of methyl-phenyl-
ethylene, methyl-p-tolyl-ethylene, and methyl-benz'yl-6thylene' gave
mixtures of glycols and aldehydes (Ref, 3)- In both casest oxonium com-
pounds formed as by-products..-The latter can react by ring cleavage and
subseiqt~ent migrat-i-Ton of the hydrogen atom or radical, or by ring
cleavagt:, followed by the addition of water (Ref. 4). Reaction of the
oxida4 with diethyl-amine gave the corresponding hydroxy-amines in yields
varying from 40 to 80., acc6rding to the-structure of the oxide. For the
format5on of hydroxy-amines, the components had to be heated in sealed
ampcules cn a water bath for 20 - 30 h. This reaction proceeds in
accordanse with Krasuskiyls ruled The authors mention a publication by
I, N. Danilov,. There are 4-tables and 7 referenam. 5 Soviet, 1 French,
Card 3/4

Studies on Unsymmetrical o