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

Document Type: 
Document Number (FOIA) /ESDN (CREST): 
CIA-RDP86-00513R001859420002-0
Release Decision: 
RIF
Original Classification: 
S
Document Page Count: 
100
Document Creation Date: 
November 2, 2016
Document Release Date: 
September 1, 2001
Sequence Number: 
2
Case Number: 
Publication Date: 
December 31, 1967
Content Type: 
SCIENTIFIC ABSTRACT
File: 
AttachmentSize
PDF icon CIA-RDP86-00513R001859420002-0.pdf3.14 MB
Body: 
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;