SCIENTIFIC ABSTRACT VENUS-DANILOVA, E.D. - VENZHEGA, A.S.

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• Collection: Scientific Abstracts
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• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
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• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

Investigation of the Reactions of Pinacols With 79-28-3-19/61
Substituted Acetylene Radicals,
XV. The Action of Sulfate of.Mercury on the ABymmetric Dimethylphenyl-
-~henyl-Acotylenyl- and the Asymmetric. Methyl-,Diphenyl Phenylacetylenyl-
Lthylene-Clycols
product could either be an isopropylivfe derivatiie of
glycol (VII) or that of a condensation oxydihydrofurfurans
(II) with acetone-1-5-dimethyl-2 4 diphenyl-2 acetonyldi=
hydrofurfuran-2,5 (VIII). The attempt to try and obtain
the bond (VIII) by condensation of dihydrofu.rfurans (II)
with acetone was successful. The heating of the acetone
solution of the compound (II) with sulfate of mercury lead
to a product 'which is identical with the one synthetized
from glycol"Mclerthese conditions. This experiment makes it
possible to acknowledge the compound obtained from glycol
in acetonr- solution under the action of sulfate of mprcury,
as being 5.,5-dimethyl-2,4--diphenyl--2-acp*cnyl-.dihydrofurm
furan..2,5. The identity of the producte obtained from (I a)
arid (11) was illvstrated by takIng tho absorption
spectra in ultraviolet light,
There are 2 figures and '12 references, lo of which are
Card 3/4 Soviet,

Investigation of the Reactions of Pinacoln With 79-28-3~19/61
Substituted Acetylene Radicals.
XV. The Action of Sulfate of Mercury on the Asymmet-ric Dimethylphenyl-
-o~enyl-Acetylenyl- and the Asymmetric- Yet hyl - D,_ph enyl -Phenyl :-. ~, ety I eny I -
Ethylene-Glycols
ASSOCIATIONs Leningradskiy tekhnologicheskiy institut imeni Leneoveta
(Technological Institute imeni Lensovet .. Leningrad)
SUBLIMED% January 2~, 1957
Card 4/4

C
AUTHORS: Venus-Danilova, 2. D.;
TITLE: Investigatior, of the Converoion of Pinacols With Substituted
Acetylene Radicals (Ia2ledovaniye prevrashcheniy pinakonov
s zameshchennymi atsotilenovymi radikalami) XVI. Synthesis
and Conversions cf the Symmetric Dimethyl--Phonyl.-Tertiary-
Butylacetylen,~.lethylenei,ylycoI (3,6,6--Trimethyl-2-Pheny1hep-
tille-4.-Diol-2,3) (XV1. Sintez i prevrashcheniya simm.,lime--
til-.fenil.-tretichnc,-.butilatootileniletilenglikolya (3,6,6-
-trimetil-2--feni..~4.Ce.Ptin--4-diola-2.3))
PERIODICAL: Zhurnal obahchey khimli, 1958, Vol. 28, Nr 6,. pp. 1477--MB2
(USSR)
ABSTRACT: At present it is still impossible to predict the direction
of the conversion of the pinacols of the acetylene series#
as every radic-al taking a odrtain position in the m,;lecule
of the pinacol influencea its converaion. The authota only
investigated the summary effect of these influerice!3. How-
ever, the results of the conversions of the symmetrical
di-r,a~uh~-1--phenyl...phenyl.-acetyler,ylethyler-e.-lycoI (Ref 4) of
Card 113 the asymmetrIL.,al me thyl. -diphenyl -tert iary-butylac, etylenyl

AV/ 791 -28-.6-9/63
Investigation of the Conversion of Pinacola With Substituted Acetylene
Radicals. XVI. Synthesis zixid Ccnversians of the Symmetric Dimethyl-Phenyl-
-Tort iary-Butylaoetylerq'i ii thy leneglyc o1 (3,6,6-.Trimethyl.-.2-.Phonylheptine--
..4-Diol-.20)
glycol(Ref 3), as well as of the asymmetrical methyl--dij,,heny1-
--phenylaoetylenylethylene glycol (Ref 5 and of the trimethyl.-
--phenylaoetylenylethylene glycol (Ref 8~ make po8uible a
predictiQu to some extent. Of these compounds the first two
yielded only enenealcohola, and the two latter ketones of the
acetylene saxies. It may be expected that the symmetrical
dimetliyl--phen.yl.-tertiary.-butylacetylenylethylene glycol
(formula VIII) on the a-;tion of sulfuric acid had to convert
to the enenealcohol (IX) or the ketone of the acetylene
series (X). In order to check this aaeumption the symmetrical
dimethyl-phenyl-.tertiary.-butyl-acetylonylglycol (VIII) was
synthesized and treated with sulfuric acid in the heat. The
only conversion product of this glycol on the action of a
30 % sulfuric acid was a ketone of the acetylene series, the
asymmetric methyl.-phenyl.-tertiary~.butylacet lenylacetone
(3,6;6-,trimethyl--3--phenylheptine--4--on-2) (X~. Iteasily forms
a semicaxbazone and the 2,4,.dinitrr;phenylhyclrazone. The
Card 2/3 structurG of this keta-ne was proved by oxidation, its infra-

7)-28-6-8/63
Investigation of the Conversion of Pinacols Subotituted Acetylene
Radicals. XVI. Synthesis and Coaversions of the Symmetric Dimetbyl-Phenyl-
..Tertiary-Butylacetyleriyletliyloneglycol (3,6,6-Trimethyl-2-Phenylheptine-
--4-Diol..2,3)
red spectrum, and by a comparison of its ultraviolet spectruw
with the corresponling asymmetrical diphenyl-tertiary-butyl-
acetylenylacetone (XI) (Fig 1). There are 1 figure and 16
references, '14 of which are Soviet.
ASSOCIATION: Leningradskiy tekhnologicheskiy institut imeni Lensoveta
(Leningrad Technological Institute imeni Lensovet)
SUBMITTED: June 17, 1557
1. Ethylene glycols-Synthesis
Card 3/3

AUTHORS: Fabritsy, A,, Venu3-Danilova, E. D. SOV/79-26 .12-14/41
TITLE: Inve3tit;.-".ti~~r. ~f the T van3firr%at ions of Sec-Tf.-rt-a-Glycclo
of the Acetylene Series UnOer the ;,,ction cf Mercury Salts
(I3s1adovaniy.--,- prevrashchonty vtorichno-tretichnykh
a-glikoley atsetilenovogo ryada pod vliyaniyem aoley rtuti)
III. 2-Methyl-1,4-Dipheny'l Butyne-'z-Diol-1,2
(Ill.'~'-inetil-'1,4-diferilbuti-).-3-diol-1.2)
PERIODICAL: Zhurnal obahchey khimij., 1958, Vol 28, lir 12,
PP 3227-3231 (USSR)
ABSTRACT: The results cf the reactiGn of another (Refs 1, 2) sec-tert-
-a-glycol of the acetylene series, of 2-methyl-1,4-
-d.'phenyl with mercury chloride and
sulfate 'Ar. alcohol solution are described. This glycol was
synthcoized according to Zh. J. Jotsich from phenyl-acetyl
carbinc! and magnesium bromo-phenyl acetylenyl:
CHI
/ I
C6115CHOITICN --~ C6H5ClIGHCOCH3---~ C6 115CHOH-COH-C =- C-C 6H5* Compound
Card 1/3 on the action of the mercury -hloride dissolved in alcohol

Investi.L;ation of thin Tranaformationg of SOV/79-26-12-14/41
Soc-Tort-a.-Glycole _~f tho Seriva und'~r thc! if Y'I-rC_,rY
S-Alts, III~ 2-Methy1--!,_j -Diphenyl 3u%rne-3-Dio1-1,2
rapidly 3erarated a white, silk.-1114) product. which on
heatirg the mixtuTa gradually entered solution so that
3--methyl.-."-,r-d1phenyl furan (Refs 6, 7-(111)) resulted as
firal product. 11, turned oit that the final product obtained
as oryotals :ontair.ed mercury and clilcrine,and that, according
tc it3 analys-Ls it cGrrespcnded to the mercurized 3-methyl-
-2,' i.pheny! Kra'
,;,-d n (II). It is considerably stable, even
does not change :)n boiling with al-'~~hol and water, and passes
to a substituted furan only if hydrochloric acid is added,
and cr. ht~ating. Bas~,d on these results it.-ay be assumed that
thq transition of the set-, tert., a-glycols of the acetylene
serjF~3 tothe substitut,~,d furan.~ takes place under the acticn
of mercury chloride by way of the nercurlized furans according
to scheme 2. There are 13 references, 10 of Ahich are Soviet.
Card 2/3

Investigation of the Transformations of SCV/75-26-1 2-14/4-1
1,
See-Tert-a-Glycols of the Acetylene Series Under the Ic'i.-,n of Mercury
Salts. III. 2-Methyl-1,4,-Dinherlyl Buty-ne--3-Diol-.1,2
ASSOCIATION; Silezskiy politekliniclieskiy institut, Folsha i
Leningradskiy takhnologicheskiy institut imeni Lensoveta
(Silesian Polytechnic Institute, Poland, and Leningrad
Technological Institute imeni Lensovet)
SUBMITTED: December 20, 1957
Card 3/3

OA
ri

J-
5.34oo
77L-17
1; C) ~,7 /7 'j - 1 -7
AUTHORS: Allbib.,,kaya, V. M., E. D.
TITLE: Letter to the Editor. Isom,--vtzatioa ,X Secondary-
Tertiary Acetylenic Ct-(Ilyiial Into a SabOtituted
/3-Furan
PERIODICAL: ZhArngl obshchey IchInill, 1~60, Vol 30, Nr 1, pp
3119-350 USS11)
ABSTRACT: 3-MethYl-5-ylienylperit.~,rie-,;-~1J.ol.-2,3 (I) lo converted,
by heatinZ-;-wIth 20-'J()% ~mlVurlc a~;Id, Into 2,3-
(III) In equIlibrium
w1th Ito eriol form (11). The f3orne rizat tort can
be represented by the Collowin,,r
Card 1/3

Letter to the Editor. Isornevizatlon of
Secondary-Tertiary Acetylenic CL-Glycol
Into a Substituted Furan
771117
SOV/19-30-2-78/~8
(Alaelloll-c-cli-c-Calls
c1l, c1l,
(_C--C C611
C113(l --6
0 0110H
clylc- --(,Oil cli'lic'---co
I ;~:t
C11311C ko 11, ("11311cl
\0/ \0/
(11) (fill
(bp of the Alran 138-138.50 (21nn); M 1~i-).6, 1838.9
(calculated 190); n 20 1.5360; 81% enol; Its semi-
Card 2/3 carbazone: mp 116-PIYO) . Int'rared spectrUIR Of

Letter to the Editor, Isomerization of
Secondary-Tertiary Acetylenic (I -Glycol
Into a Substituted a -P-Aran
ASSOCIATION:
SUBMITTED:
77417
S 07/7 9 -30 - 1 -7,8/7 8
furanone h1d the followino absorption bands- carbonyl
(1,709 cm- ), double bond (1,6,23 cm-11, eth;r oxygen
in the tetrahydrofuran ring OX3 cm- ), and hydroxyl
(3,440 cm-1) Uae of Absorption Spectroacopy in
Chemistry--Primeneniye spektroskopii v khimii--IL
(1959). Ther2 are 3 Soviet references.
Leningrad Lemoviet Technological Institute
,'(Leningradskiy tekhnologicheskiy institut imeni
Lensoveta)
October 3, 1959
Card 3/3

5.31100

AUTHORS i Pavlo-va, L. A., Ovlova, A. H. ._ Veriu,,;-D,tiA1 D.
TITLE: Concerti-i-rig th4-2 of
Hyd roxyp) i t1ja la i i a i id 5, 1)1 D-! 1 -1 1
dihydrofuran-2,5 With Acotic. A"'1hydrNi-1,
FERIODICALt Zhurnal obshchey Ichimil, !960, Vol -10, N- '-1, oP
--) .
(USSR)
ABSTRAM This is the continuation of in%restigatuions of
densation of hydroxyhydrofurans and hydroxyphthalans
with acetone, pheny1methylpyrazolone, and other ccr,-,rjc)ur,,ds
'
C51
this journal,Vol 26, p 884 ~1956); ibid. , Vi 2~3, P
R
958)j ibid., Vol 29, P 158~j (1959). In th~-,- pr-----c--nt
t
-diTnetliyl-l-pl)enyl-l-hydi,oxyphtla~,., 11 ,..a
study, 3,3
condensed viith acetic anhydrido an Loilin,~, for hr in
the presence of pyridino. The reaction gavii.
-1 -11 J
dimc-tiiyl-l-pht~ziylplit-.h--ilyi-1) acetl,-, zacj.d (11, yl~'ld -'5%;
i
0 106-1070 C, from ethyl other + InfAr(Acilm eth~,v) and
m
.
o-isoprope,-i,~,,~'t,enz,ophenoiic, (IV, yield 52.4'i-), mp 42-430 C,
Card 1/5 from methanc.- dilute). The lat'Ler -,-ias for-ied as a res,.;lt

Concerning the Condensation of 3,3-Dli-,iuthyl-l- 78251
Phenyl-l-Hydroxyphthalan and l,-:-D!met!%,rl-
2,LI-Diphenyl-2-Hydroxy-di~,,-~dro~.';irE.,ri-2,5
If
Acet-lc Anhydride
of the dehydration of th,-~ open
of phthalan I.
Ml
[Al
\0/ clqll~
(I V)
Card ~/5

Concernin the Condensation of 3, -1-DI.mf,, IJ iYl-l- 78251
9 j C-O-J/ 7~~_ _:~Ii' '~
Phenyl -1 -fly droxyphtlialan and 5,5-Diraethyj.-
2,1~-Diphenyl-2-H,ydroxy-dihydrofi.ir,in-2,5 ',,Ilth
Acetic Anhydride
The condensation of 5,5-dl.metliyl-2,1~-dipheriyl-2-oxydi-
hydrofuran-2,5 with acetic anhydride gave (5,5-dimethyl-
2,4-diphen 1-2,5-dihydrofuryl-2) acetic acid (VI, mo
137-1380 C~) and not acid M a~,3 suggested pre-viously
by the authors (this journal,Vol 23, p 681 (1953).
c1l,
C,1115
Loll
(V)
C4115-c-r'll
py,(1; Villcooll
.\, ll;~\Cllils
0
(VO
Card 3/1~

Concerning the Condensation of ~,3-Dimethyi- 78251
-1-Phpny1-1-IIydroxyphtha1an and 5,5-Dtn- S 0 V //7) -5 /6
ethyl-2,lt-Diphenyl-2-Hy(droxy-,Iihycl.-o-li,rar,-2,5
With Acetic Anhydride
--cl 1
G~
()/ 1 0,
(VII) (VII
(c,00102 + C41Is-C~=Cll-C-CtIl5
I !I
Mf I Q (Vill)
co, + Cuilzcocoml
:(2) C 115
CO
(2)
c"ll,cooll + ll(IOC-(
i Oil
I (I X)
('015COC0011 ~ (G0011)2
Card 4/5

CO I W e I'L I L I iL110
2, 4 -Diphonyl -' 1-Hydi-oxy
Acetic Anhydrld,~~
ASSOCIATION:
The ,Arlioturc-, o1' VT Its
ox1dation t;lth pota~-~.Pltn Thu pr1n).ary
prodiict oC thf,, hydroxyke'lo-acid (X),
00111d 1-101, be ~11t-'J)~IV:M(2(t :t;l it rapldly Ln 2
d1.v,--c,1Jon~.; (Viii, ytf~-].d
') and ()YE11-11c (I ~2 ;! Id
X6 d 'I c
3
Ix -, yiclcl ,itid lw.-n~:olo %t~Ld. Th~-,r-- a-r~wl 2"
~? U. E. 'L) Fv,,-,nch, I Dutch, P) G-nrnn,
ovalv, I "I
U., . arid U.K.
ar--: J. L. I'lleArl, W. F, lhi-t, J. A:n. Chem- Soc-, 59,
c- I)
719 (1937), J. E. J. ChQM. '30c., 3W4 (irl-fl;
F~. Parn~:!tto J. Tv". I. G. Nixon, J. ch-.2m. soc.,
kt (19'27); E. 11. If. C. Walter, J. Am. Chem.
Soc., 70, 3702 (1948).
Lensoviet Leningrad Tachriol-ofrical Institute (Leningrad-
siciy telchnologichO21cly Institut Imeni L,:nso,.,eta)
SUBMITTED., D-acember 30, 1938 Card 5/5

ANTONOTA, A.A.; _T; nJ5:P#1q1pVAm S.D.
Conversions of pinacones vith substituted acetylene radicals. Part
18: Synthesis and conversions of uns7a. meth.71diphenylvinylacet7len-
ylethylene glycol (2-noth7l-1,1-diphenyl-5-hexen-3-yne-1,2-diol).
Zhur. ob. khim. 30 nc.9:2872-2877 5 160. (MIRA 13:9)
1. Loningradakiy tokhnologichookiy institut imeni Lensoveta.
(Hezen.vnediol)

S/079/60/030/009/015/015
BOOI/BO64
AUTHORS: Danilov. S. N., Venus-Danilova, E. D., Orlova, A,
Yegorov. A. G., ka z i m-1-f ZVW-,-r-. -t-,
TITLE: In Memory of A. I. Bol'shukhin
PERIODICAL: Zhurnal obshchey khimiij 1960, Vol, 30. Ito; 9,
pp. 3145-3147
TEXT: A. I. Bollehukhin died or November 14, 1959, An outstanding peda-
gogist, he ranked among the best teachers at several institutes of Lenin-
grad University. A son of peasants, he was born in the Government of
Vitebsk on February 20, 1906. At the age of only fifteen he was already
allowed to frequent the preparatory classes at the physical and mathemati-
cal department of Leningrad University. Ile worked himself throuCh his
student years as a laborer and a clerk, and later was a laboratory assis-
tant at the Tuberkuleznyy institut (Institute of Tubercolosis). There,
under the guidance of E. D. Venus-Danilova he was able to complete his
graduation treatise on the synthesis of thyroxine (Ref. 1), which gave a
description of the intermediates 3,5-diiodo-4-(41-ethoxy phenoxy)-nitro-
Card 1/3

In Memory of A. I. Bol'shukhin 3/079/60/030/009/015/015
BOOI/BO64
benzene; 3,5-diiodo-4-(4'-ethoxy phenoxy).-aniline along with his hydro-
chloric salt (Ref. 1). After graduation he worked out an original method
of determining acetyl cellulose-bound sulfuric acid at the Inotitut
drevesiny (Wood Institute), at the laboratory headed by 11. 1. flikitin
(Ref: 2~. He collaborated in the synthesis of soluble cellulose triacetate
(Ref 3 . As an assistant, he worked in the field of general, inorganic,
and organic chemistry at the Lesnaya akademiya (Academy of Forestry), at
the Komvuz imeni Stalin, at the Zootekhnicheakiy institut (Zootechnical
Institute), and at the Leningradskiy gosudarstvennyy universitet (Lenin-
grad State University). He submitted his diasertation for the degree of
a Candidate of Chemical Sciences at the Leningradskiy tekhnologicheskiy
instlz-.,,' im. Lensoveta (Leningrad Technological Institute imeni Lensovet),
During the war he headed the laboratory of the Glavnaya vodoprovodnaya
stantsiya (Central Hydrological Station) in Leningrad, and, later, the
Trust "Lenvodoprovod". From 1943 on he was a docent at the Pedagogicheskiy
inatitut im. Gertsena (Pedagogical institute imeni Gertsen), and at the
Leningradskiy pedagogicheskiy institut (Leningrad Pedat,,,ogical Institute).
After the two institutes were merged he was appointed docent of the Chair
of Inorganic Chemistry. A list is given of his writings a part of which
was worked out jointly with E. D. Venus-Danilova, A. 11. Orlova, A. G.
Yegorov, N. I. flikitin, T. It. Rudnev, It. Ya. Solechnik, S. G. Avraamov,
Card 2/3

In Memory of A. I. Bollshukhin S/07p/60/030/009/015/015
BOOl/Bo64
Ye. P. Brichko, V. L. Zhitorchuk. Thero are 1 figiire and 20 Soviet
references.
- 6
Card 3/3

VENUS-DAMILGV. E.D.
Action of mercury salts on acetylenic pfglycols. Trudy LTI
no.6002-48 160, (KURA J4:6)
(Mercury salts) (Mycols)
.il

ANTONOVA, A.A.; VENUS-DANILCVA, E.D.
Investigation of the conversions of pinacols with substituted
acetylene radicals. Report 16: Synthesis and conversions of
unsym-dimethyl phenyl -An~lacetylenyl ethylene glycol (2-methyl-
3-phonyl-6-hepten-4-yne-2,3-diol). Trudy LTI no.60s85-91 060.
(MIRA i4s6)
1. Kafedra organicheskoy khimii, Leningradskogo tekhnologicheskogo
4~nst'ituta imeni Lensoveta.
(Heptenynediol)

ANTONOVA, A.Aw;_V,F21US-DAN1LOVA, E.D.
ConveroionDof pinacones with substituted ar.-itylene radicals. Part 9:
Reaction of dimethylbenzoy.11carbInol with vinylacetylene in the presence
of sodium amide In liquid rLmimonttn. Zhur.ob.khim. 30 no.101~263-3267
0 161. . (KIRA 14:4)
Is Leningradakiy tekhnologicesk-iy institut im. Lensoveta.
(Acatophenone) (Butenyne)

PAVLOVA, L.A.; VENUS-DANIID-vA. E.D.
Hydrox7dih7drfurans. Part. 7: Condensation of 5;lldizetb7,1-2,4-di-
pbonyl-2-bydrox.v-2,,5-dihydrofuran with dieth7l malonate. ZhIli.
ob. khim. 31 no.4%1-150-U54 Ap 161. (141RA 1l+ - 4)
1, Laningradskiy tekbnologicheskly Institut imeni Lensoveta.
(Furan) (Malonic acid)

SFERKOVA, V.I.; ANTONOVA, A.A.; VENUS-DANILOVA. E.D.-
-
New type of 2-hydrorj-2,5-di~tydrofuran condensation. Z~ur.ot.~tim.
31 no-9:3141-3142 S 161. (MIRA 141:0~)
1. Leningradskiy tpkhnaloricheskiy inFtitut Imeni Lensoveta.
(Furin)

SLRKOVA,, V.I.; ANTONOVA, A.A.; VENUS-DAIIIILVA, E.D.
Conversions of pinacones with substituted acetylene radicals.
Part 20: Synthesis and conversions of anoym. dimethylpheny1mothyl-
mothylacetylenyl ethylene glycols Zhur.ob.khim. 32 no.6tl771-1778
Je 162. WIRA 15:6)
1. leningradakiy tekhnologlcheskiy institut im. Leningradskogo
Soveta.
(Ethanediol) (Acetylene)

VENLL%.IDANILOVA,_E,,D,; ALIBITSKAYA, V.M., F.'UNTSEVA, Z.V.; VOROBIYEV, LJ'l.
v
"onver-sions of secondary- -tertiary acetylenic. cfglycols
under the effe-~t of sulfuri,~ acJd. Zhur.ob.khlm. 32 no.7:21-18-
212-2 JI 262.. (KIRA 15:7)
I. Lemingradskly tekhnolo[;ichefjkiy iristitut imeni Lensoveta.
(G:~Tol*)

PAVLOVA, L.A.; YAKOVL".V) S.V.; VENUS-DANILOVA, E.D.
Transformations of pinacols with substituted acetylenic
radicalo. Part 21: Synthesis and transformations of
2-math:(L-3-phen7l-5-p-tolyl-4-pent7l3--2,3-diol.
Zhur.ob.khi-. 32 no.10:3260-3265 0 162. (14IRA 15:11)
1. LeaLngradakiy takhnologichookiy institut imeni.
Lensove ta.
(Glycols)

)MIFMIYEVAP T. G.; PAVLOVA, L. A.; VRJUS-DAHILOVA
--I E. D.
Hy"Irox7d'hydrofuranm- Part 8-- 3,,Ikimtb7l-tort-butylacet7lonyl-
1-bYdroxyphthalan. Zhur. ob. Ichi4. 33 no.l.-55-59 163.
(MIRA 1.6: 1)
1. Ieningradakiy takhnologicheaki3r institut iment Lenaoveta.
(Ilhthalan)

?ELENTIYEVA, T,G.; PAVLOVA, L.A.; -Xi~jqS-DANILOVAt E.D.
Hydroxydihydrofurans. Part 9.,
3,3-Dinothyl-l-pohnllacotylonyl-l-hydroxjrphthalan. Zhur.ob.khim.
33 no,6tl851-1857 Je 163. (KRA 160)
1. Leningradakiy tekhnologicheakiy institut Imni Lensoveta.
(Phthalan)

WLENTITEVA, T.G.; PAVLOVA, L.A.; VENIJ&-DANILOVA, E.D.
Hydroxydihydrofurans. Part 10:
3,3-dimethyl-l-p-tolylacetylenyl-l-hydrox,yphthalan. Zhur.ob.khim.
33 no.7:2126-2129 Jl 163. (14IRA 16:8)
1. Leningradskly teklinologicheskiy inatitut imeni Lensoveta.
(Phthalan)

MELENTIYEVA, T.G.; PAVIDVA, L.A.;
Hydroxydihydrofurans, Part lls 3t3-dimethyl-l-mothylacetylonyl-l-
hydroxyphthalan. Zhur. ob. khIm. 33-no.8:2548-2552 Ag 163.
(MIRA 16:11)
1. Leningradakiy tekhnologicheskiy institut imeni l4s3oveta.

ATITOIICVA,,, A.A.; WMS-DANTLOVA, E.D.
Tranaformatl~on of pinacol.,j with erubst-l't-ited as-evleni--t rad-',:-a'~
Fax'I 21.z SlynthAsIs and transformations of asy=.
d=ethylph6nylisopropenyla-;et7lenyl ethylene glycol. Zhur. ob.
krlr. 34 now:~,!18:-.218) n I~tL (141RA i738)
-1. Lmlngradskiy tak~aiolcgl~-hevk~'y instlltu4l ime-n! Lens,)veta.

MELENVIEVA, T.G.,, PAIIWVA, L.A.- ~TENUS-DAYILOVA, H.D.
Pydrorydih7dn,;.*aianF. Paz` '1;-. Bvii-. I-opert..ies of the iaomtri-
zatlon FT-OdLl-;t9 of a-e4yienicc nydroyyphthaJans. Zhur. ob. khim.
34 (MIRA 17.-8)
'k"i:r s t,l- tu t
en nqo. ta.
Leningrad~t-'-j Y.-~kh=log! h~!c in in Le ve

ORLOVA, A.N.; PAVLOVA, L.A.; VENUS-DANILOVA, E.D.
Hydroxydihydrofurans. Part 13: Condensation of 3,3-dimethyl-i-pbenyl-
1-hydroxyphthalan and 5,5-dimethyl-2,4-diphenyl-2-hydroxy-2,5-dihyd-
rofuran with malonic acid. Zhur. ob. khim. 34 no.10:3265-3270 0 164.
(MIRA 17:11)
1. Laningradskiy --osudarstvenn)7 pedagogicheskiy institut im. Gerstena
i Leningradskiy takhnologicheskiy institut imeni, Lensoveta.

SERKOVA, V.I.; PAVLOVA, L.A.;.~TTS-DAXILOVAJ, E.D.
Transformations of pinacenes with substituted ac,,*tylenl~=
radicals. Part 23., Synthesis and trarsformation of non-
symmetrical dimethyl-tert-butyl-.phenylacetylenyl ethylene
glycol. Zhur. ob. khim. 34 no.110624-3630 N 164
(MMA 18A)
1. Leningradskiy tekhnologicheskly Institut imenl Lanscveta.

DANILOVI S.N.; gj--. rpd.- AHBTJZOV, A.Ye., rod.,- VVEDkII.-:KIY, A.A.,
red.; VENUS-DANIWYA.,_Z.D.j, red.; ZAi'IW,-,OVA, A.I., red.;
IOFFF, I.S... red.; KAVERZNEVA, Ye.D.,, red.; LUTSE2iK0, I.F.,
red.; MISIICIOIKO, K.P., red.; 11FITSOV, M.S., red.; PETROV,
A.A., red.; FREDLIVA, R.Kh., red.; .31111-INAKIN, M.M., red.;
SHUKAREV, S.A., red.; YURIYEV, Yu.K.,, rod.
(Biologically active compounds] Biologichooki aktivriye
soodineniia. Moakvao Naukay 1965. 305 P. (XIIIA 18:7)

DOULOV, rlwv, -;~A.: ZUHAIVIA, A.I... rod.; Xti;UZOV, A.Yo.)
re-1 VVE-, i-'l 1 A A ~ , 'M ~'IJ ~~ . J.
-.D.-%':JLO'lh., B.D red .
LF- rf-cl.; K.Fl; n.d.; lilNTSEV, I..S., red.;
FETRbV, A.,A.t rrt,'~ H"EMLITIA, R.Kli., rod.; ljfq't,iYAKTN,
rerl.. SHCHUKAh-EV, Li.A., rf,.I,, YU101TV, Yu.K.,, red.
fpcobigm.", Gf orp"anic S,'lltnesis) Prolblemy Orgsim-cheskego
ointeza. Nauka. 1965. 323 p. (1,1111CA 18~8)

POLVIA, L.A.; VENUS-DANILOVA, YEll,"ISOV, A.V.; ORL911%, A,N.
5,5-Diynethyl-2,4-diph-~nyl 2,5-d1hydrofuran. Zhur. ob.
35 no.9:1690-1691 S '65. (MIRA 18:10)

MCHW, G.I.; GRIGOIYEVA. A.Go; VMMTO-V, N.V*
Effect of live virus concentrations in anti-influenza-yaceine
on its immunological activity [with summary in English] Yop.
virus 3 no.6:357-362 N-D 158, (;IRA 12:1)
1. Leningradskiy nauchno-iseledovatel'skiy inatitut, vaktain t
a7vorotok.
(My ]III 7A, immunol.
vaccineq eff. of live virus concentration on
imm=olj qualities (Rue))

VEN I- YAMINQY,*__-A-N, , red.
[New wrieties of fruit in the central region of the European
USSR and the UkraineliNovye aorta plodovykh kulltur srednei po-
losy Evropoiskoi chasti SSSR i UIrrainy. Yoskva, Izd-vo Mosk.
univ.1 1961. 462 p. (MIRA 15:12)
(Frult--Varieties)

VENIYAMINOV, A. N.
20890. Venlyaminovp A. N. Michurinskoye ucheniye v deystuii (Iz praktiki selektsii
mestnogo sorta slivy skorospelki) Sa-!. i ogorod, 1949, No. 6f s. 12-1h.
SO: LETOPIS ZHURNAL STATEY - Vol. 28, Moskva, 1949
19

1. VE10YAMDOVp A. N.
2. U&SR (600)
4. Cherry
7. Clonal selection of the cherry. Agrobiologiia no. 5, 1952
9. Monthly List of Russian Accessions, Library of Congress, January -1953. Unclassified.

1. VENIMINIMV, A. ~!., I-rof.
2. USSR Wil
4. Cherneriko, Serrar, Fedorovich, 1877 -
7. Anniiersrivy of an outstanding p1tint brps&-r, Sad i oC. , 'To. 11, 1952.
11
)5'1. Lnclassified.
9. Voonthl Li3t of Rus.,Aan Acceg,.,!,)ns, Library of ConCirers,, v,

VENiyAMINov, A.N., professor.
, I.- I I - ~-.: .1.1 . Priro" 43 no.8:109-111 Ag 154.
Apricot In the central zone (MLRA 7:8)
1. Voronazhakir se1'akokhoz7a7stvenn7T institut.
(Apricot)

VEN-JAMINUIV, A. N.
Cherrie andplums
Yoe',.-va, Gos. zd-vo sel;