SCIENTIFIC ABSTRACT YURYEV, YU. K. - YURYEV, YU. K.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001963220016-1
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 19, 2001
• Sequence Number: 16
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

M
884n
S/079/61/031/001/013/025
B0011BO66
AUTHORS: Novitskiy, K. Yu., Volkov, V. P., Shayderovv.$ L. P., and
Yurlyev, Yu. K.
TITLE: Studies in the Furan Series. XI. 2,5-Bis-(chloro-methyl)-
furan in the Synthesis of Symmetric 2,5-Dialkyl Furans
PERIODICAL: Zhurnal obshchey khimii, 1961, Vol. ~31, No. 1, pp. 136 - 139
TEXT: The authors synthesized the symmetric 2,5-dialkyl furans by the
reaction of 2,5-bis-(chloro-Ryethyl)-furan with organomagnesium compound.9
in yields 3f 33 - 16 ~,. They found the yield to be highly dependent on the
length of tho oarbon chain and on the nature of the halogren of the alkyl
magnesium halide. The maximum o do of dialkyl furane were obtained with
alkyl maenesium chlorides (46 ?'iYiw1ith propyl magnonium chlorido, find
38 0/'~- with butyl-magnesium, ciil-oride); when using alkyl magnesium bromideo,
the yield drops to 37 0~~ with priojiyi magnesium-bromideq--andto 29 ~ with
butyl magnesium bromide; when using methyl magnesium iodide,-the-yield--is
only 5
card 1/3

Studies In the Furan Seriou. X1. 2,5-Bis- S/079/61/031/0.01/013/;925
(ohloro-methyl)-furan in the Synthesis of BOOI/BO66
Symmetric 2,5-Dialkyl Furans
1. RCH -CH R
3~ 2 0 2
101CH2wA CH 2C 1 - '~~?
\0 (1) -1 R I oil CH2 R
R = CH V C2H5' n-c3H7' n-C4H9' iso-C 4Hq;.R' = 02H51 n-C 3H70 n-C4H9'
Attompta with Grienard roagant,,j from n-octyl bromido, bromo benzene,
benzyl chloride, cyclopentyl- and cyClotwxyl ohlorido were unsucce0oful.
5 ~c diphenyl and symmetric diphenyl ethane (18 -10 Wero uoparatod w1th
phervl magnesium bromide and benzyl magnesium chloride respectively. In
the reaction of methyl magnesium halides with furfuryl chloride (Ref. 7)
a polycondensation mainly occurs, which yields the polymers presented in
Scheme 2. The yields of the corresponding dialkyl furans in the reaction
of 2,ic-bis-(chloro-methyl)-furan with lithium alkyls were 19 - 25 ~c.
There are 9 references: 4 Soviet, 1 French, 1 Canadian, I British, and
3 US.
Card 2/3

Studies in the Furan Series. XI. 2,5-Bis- S/079/61/031/001/013/025
(chloro-methyl)-furan in the Synthesis of 30011B066
Symmetric 2.5-Dialkyl Furans
ASSOCIATION; Moskovskiy gosudaretvennyy universitet (Moscow state
University)
SUBMI'TTED: February 22, 1960
Card 3/3-

NOVITSKIY# K.yu.; VOLKOV, V.P.;,,,.~Irb-vu -YU-K-
Furan aerie-s, Fart 12.* Fuian-215-dialdehyde and its reactions
witE malonic acid deri,~atlves. Zhur. ob. khim. 31 no. 2:53:1.2-
541 V .161. (MM4 14:2)

-KOROBITSYNAl I.K.; INICHENI-12 (Yin Chl-;ti-IJLehl; YM I YEV Yu K.

Reactions of the nethylene, group of 2,20J5~-tetraalkyl-3--
furanidonese Zhur. ob, khim. 31 no.3:836-840 IvIr 161.
(HIM 14:3)
1. Moskovskiy gosudaratvennyy universi-tet.
(methylene group)
(Furan)

I
I
-
a
P
yl.~ .

YURIM Yu,K.; ZEFIROV, N.S.
Furan series.. Part 3./+:.'React-5vit;r of &-oxidee of the 3.,5 e-"do-
3.,6-eudoxocZbhexane aeries. Zhur. ob. kh1m. Yl
o. (MIRA 14:3)
P 0:84MA4 Mr 161.
1. Moskovskik gosudarptvennyy universitet.
(Norbornene).

YUR IYEV, YA.K.; PM-I7M'O,, O.MO
Catalytic conversions of heterocyclic compounds. Part i57: Car,
version of 2-alkyltetrahydroaraw to Z-aJ41pentazwrthYlene sulfides
ZhuroobAhimo 31 no.W883-1885 Jo 161- (KMA 140)
le Mbskovskiy gosudarstvemiyy universitet Imeni H.Mommosovae
(Pyran) (Nothylene sulfide)

7mm
fg
"t
4
~

1AIMa IN TAM ts RaflA � iMmu
yURtyLVA YU.K.; EKNOMT# D.
and -thiophene 7Anr.ob,khlz.
2-Cyclopropyl- and 2-PrOpenyl-furan (mm 14:10)
31 no.lo-.3274.,3276 0 161.
H)okovskiy gosudarstveruqy universitet imeni m.V.Uimnosova.
(cycloprow- e) (puran) (Thiophone)

NOVITSKIY, K.Yu.; VOLKOV, V.P.; SHAYDEROVAO L.P.; YURtYLV, Yu.K.
Fumn series. Part 28: 2, 5-DIs611--alkylazomethin )- and
2,, 5-bia(K-arylazomethine)-ftLranso Zhur.ob,khim. 31 no.10:
3277-3281 0 161. OaFA 14:10)
1-0 Maskovskiy gosudarstvennyy universitet imeni H.VAcconosova.
(Furan)

S/079/61/0.'1/011/003/015
D202/D305
r0
AUTEOM s Yurlyevt YU, KIF Zefi Y, N. S., and Gurevich, V. M.
TITLE: Investigation of the furan series M. The reaction
of 2-vinyl furans with cx. -unsaturated ketones
PERIODICAL% Zhumal obahchey khimii, v. 31, no. 119 1961p 3531-3534
TEXT.- In this work, the authors found that i-vinyl. furan reacts with
v- I P -unsaturated ketones which have a substituted methyl group, in the
presence of traces of H 2 s04 as a catalyst, according to the schenie:
R-CH--GH-1\j + CH2j-C0CH3
0
FICHI-CIH-COC113
R-CH=C11- \O/
la R R'=11'. 16 RCtll,, R= H; 10 R11 It'= C116
Card 1/ra

S/07DJ61/031/011/003/015
Investigation of.,.. D202/D305
where R = H, or C 3H7 Rl H o r CH3 Similar furan derivatives
react in the same way; as these reactions proceed with the forination of
1'esinous side-products, the yield is low, but the method is considered
an easy way of preparing furan ketones. Ketones substituted with 2-furyl
acetylene were not prepared. The ketones obtained react -with rzaloic
anhydride giving additional produets* Hydration of the vinyl side chain
of furan. proceeds smoothly when p alladium or WO 4 are uced as a
catalystp and it is easy to obtain an additional product linked to the
furan -vinyl double bond. Freparation of the. following compounds is given:
2-vinyl furan, by a previously known method. Reaction of -zinyl furan with
thiophenoit a mixture of 4.2 g of thiophenol and 3.8 g of vinyl furan
was left in a closed vessel for a few days; the product diatilled in
vacuo yielded. 7.5 g of sulfide (92%); b.ps 1.46 - 1480C (6 mm);
20 20
UD 1.5811; d 4 1.0017; AIRD60.88, calcul. 60.22 * C 12H12 03 F 5
f~&bstracterls notes " F "probably means fraction-7, 1-(5-vinyl furyl-
2)-butanone-3 (cpd. Ia). To a flask containing 0.2 g of hydroquinone,
Card 2/5

S/079/61/031'/011'/00-3/015
Investigation of,,. D202/1)30'5
14 g of mothyl vinyl acotone and 2 drops of cone, 11,S0 14,1 g of
0 V
2--vinyl Ittran was added (at r~ 2.1 C), T110 M i X. W 1'Q WAIR .4 L i I'VO 11 rO r I
hour, diluted with etherg washed with NallCO3 and water, and dried over
%uh. MgSO4; the yield wag 5 g (2O.5A) after distillation in vacuo fa it
1.
stream of nitrogen; b.p* 109-1100 C (5 mm)~ nD20 1.5171; d4 20 -'-00303'.
1% 48,,22;calcul. 46.39 The additional product of la ketone xad
mal.zlc anhydride-. 0.82 g of Ia itas added to a concentrated solution
of 0.49 g of maleic anhydride in absolute ethep after 12 - 15 haurpl,
white crystals were formed,, with bp* 110 -- III C (from benzene)o They
decomposed after a few hours in contact with air. 2-:-methy1-).-('5-vinyl
fury'l-2)-intanone-3 was obtained in the same way, as compound la, from
14.1 g vinyl furan and 16.4 g of methyl iso--propylene ketone, yielding
5J g of the products b.p,, 105 - 10'70(0 MM); n D20 10080! d4 20 100390Z
MR 52.16,scalcu'l~ 51.01; C H Op. . By the same method, .1-0--vinte-
D 11 14
Card 3/5

S/079/61/031/011/003/01 ~5
Investigation of... D202,/D305
nyl-l-furyl-.2)-butanone-3 was obtained from 20.4 g pentenyl fur-an ani
14 ir methy). -vinyl ketone; the yield = 6.8 g (23%); b~p. 121 - 122o (5 mm)7
a 20 1,50814 4 20 1.10511, WIn 62,29;calcul, 60.29 2-6thyl ruran Was
D 4
obtained froet 9~4 g of vinyl furang kidrated in 50 ml of methyl alcoho)
-with 001 g Pd on BOS04 (15% Pd). After the amount of 11,; -equivalent
to one double bond has been absorbed., the hydration retiction stopp-A
abxruptly~ The yield ~Fas 8.1 g physU~a:t properties vf-Tz, in gDoJ
agreement -ith data given in Weatern literature..
butanonc--3 was prepared by tvo methods, (a) 3.5 g, of kc~tan,_, I-) I ri
40 ml of met.haq,~ vi-,,r,~ hvilratk-). aaq abo-q-, qif,b yield ot 2,,9N g
b.P. 95"(f, wM)., n 20 .1,47261 d 2 0 011 9DR6 ) lift 4(~,CVJ c-,ql eu I . 46,,5,,IS
D
(b) From 9,,6 g of etkyl furan and 10o5 g metby) Vinyl keton-
00A 5 wl of concentrated 'R SO by o. -i-tho-I desteribyd pr.?-viou!~Iy ffr irh~
2 4 1
Preparation of 2-methyl furan,, 8.6 g if compound -L&,ntical with thai
Ca~,d 4/5

Investigation of... D 2 0 251/M 015
Obtainpil by method (a) given above,~ The above- experiments provi- tbat. tb~
r~~actinzis of alkenyl furans with unsaUtrated 'ketones belong to the typ~-
of addition-substitution oneso There- are 1.13 referetrr,,,~SZ 6
and 9 non-So7iet-bloc, The 4 most recent references to the Eng.Ai~-h-
language publications read as follows-~~ J. WeW G. Porcherdt., ij,,S,- Pat-
2~640;057 (1953); J~ Bachman, L, Hei-gey, J~ Am~ Chetzi~ Soc~ 71, 1095
(194951 D~ Coffm'rzn ', P. Barrick, R, cretl~er., W Rep--At-! J - Am, Clictri
TI; 490, (19,19)! E, BrE-ault, 0, Dremf,-r, Ch, A~~ 43; 201.5
ASSOCIATIONI~ Moskovskiy gosudarstvonnyy univerait-,~ im.41, V., Lomon,).cjo1;,,I
(&(oscow State Universitv im M, Lomonoso,)V)
SUBMITTED! December IG. 1~1160
CaTd 6/5

SADOVAYk., NA
Chemistry of selenophenes Part 34: Reduction of ketones of the
selenophene serieso Zhur. ob. khim, 31 no. U0535-3536 N 161.
(MIRA 14111)
1. Moekovskiy gosudarstvannyy universitet imeni M.V. Lomonosova.
(Ketones) (Salenophene)

YURI vjju~ EUXURDT, D.
Synthesia of heterocyclic amalogs of stilbene. Zhur. ob. khim.
31 no. 11:3536-3539 11 161e (MMA 14:11
1. Moskovskiy gosudarstvonnyy universitet*
(StUbsna)

Jolivat's work "Study of 3p6--andoxo- 4t-tetrahydrophthalic
anhydride" reviewed-by W.K.lUrlev., N.S. Zefirov. Zhur. ob
khim. 31 no. 11:3840-3841 N f6l. (KtRA 14:11)
I., Moskovskiy gosudarstvennyy universitet,
(Phthalic anhydride)

I.K.; YMttt.'YEV X4 IN' CHENI-LE (Y-In Chien-lel;
~yu
DAVYDOVA;. GAYDAMUCHi N.N.
Fl=anidino-pyrazoleas zhtwoobokhim., 31 no.22:3921-3926 D 161.
(KM 15:2)
is)
~=O)

BALMIDINS A.A.., akadenik~ red.; ODOM, 14-10p Prof., red.; LEBEDEV,
V.P. ALITSEVI A.1%,, za--. red.; AGR("(Yv'OV,#
ftts.# iarm. red.; Y
*V#p prof., redo; Y[R!:IZV
Me.., dots.$ wn. red,; TomIYEVA, K --,&-
Yuji... prof.j red. PANCIMMOVP G.1,10-0 prof.j red.; SOKOLISKIY,
D.V., akademik, red.; VOLlymommiN, F.F.s prof.p red.IIAZAIINA,
LV.,, tekbn. red.
(Catalysis in the institutions of higher learning; papers of the
First Interunivervity Conference on Catalysis)Kataliz v vysshei
shkole; trudy. Moskvnp Izd-vo Mo-ik. univ. No.1, Pt,2. 1962.
325 P. (WRA 15: 10)
1. Mezbmmmvsk6~re soveshchaniye po katalizu. lst, 1958. 2. Ake-
demiya naWc Kazakhskoy SS;,, (for SokolIskiy)v~-~,i-*KtdmIcU=ski7 fa-
,kulltet Moskovskogo gosudar6tvemogo univeraiteta (for Yurlyev).
(Catalysis)

YURIYEV. Y o MAGDESIYEVA, N.N.
(i -Acetyl-2-acetoselenophene (selenenoyl-2-acetone)
and C.)-trifluoroacetyl-2-acetoselenophens (selenenoyl-
2-trifluoro aceione). Fet. poluch. khi . reak. i repar,
no.6:5-9 162o ~HIRA 17:5)
1. Mookovskiy gosudarstvennyy universitet.

YURIYEV. .; MAGDESIYEVA, N.N.; TITOVp V.V.
_P~~u.X
1,3-Dibenzoyl-1-3,-di-(2-selenencyl)-propane. Met. poluch.
khim. reak. i prepar. no.6:9-11 162. (MIRA 13:5)
0 ,

-;lRl ~Evyu- K.; PENTIN, Yu.A.; Revenko, 0,M,; LEBEDLTA . E. I.
2.,3-DialkylpentamsthAene milfides and their infrared aboorptlon
spectra. Neftekbiala 2 no.2:137-143 lir-AP 162. (MIRk 15:6)
1. Mookovskiy gonudarstvermyy universitet Imeni H.V.Lomonosolraq
khimicheskiy fakulltet.

WRIYEV, Yu.K.; MEWITSOVA, N.N.; TWHGHCVAp Ya.G.
Haman spectra of 2-propyl-, 2-cyclopropyl-,, end 2-propen-7-1-eleno-
phone. Vest.14ook. un. Sor,2:khim. 17 no.100-62 J&-F '62.
- (MIRA 15:1)
1. Moskovskiy gosudarstvemVy universitet., kafedra organicheskoy
khimii i laboratoriya molakulyamoy spektraskopii.
(Selenophene--Spectra)

DIELICHAKOVA, N.V.; MEZENTS OVA9 N.N.1 FEN AN CPIe^ng Ang); PESHK07AV' V.M.;
YUR I M Yu. K.
V
Charaeteristics of some A-diketones of the aeledophe-na series.
Vest.Mbsk. un. Ser.2:khlA. 17'no.1:63-67 Ta-F 162. (MIRA 15'-l)
1, Haskovskiy goaudarstvenny~ univeraitet, ketedra analitichaskoy
-khimii.
WaE~Iophene)

Synthesis of 3-alkvitetrabydropyram. Veqt.Yask.un.Ser.2.- Khi=.
.17 m.2:68..71 Mr-Ap 162. OP&M 15:4)
11 Wedra organicheskoy khJmjj 140skovskogo universiteta.
(Eyran)

FBI fill r8a
016 ~~I, . t4l~ 7tmi

NOVITSKIY K.Yu.; VOLKOV, V.P.; 'YURIYEV, Yu.K.
Fsaran series. Part 20; Reactions of condensation, oxidationt
and reduction of furan-2,5-dialdoWe., Zhur.ob.khim. 32 Vo.2:
399-402 F 162, (MIRA 15: 2)
1. Mooko.vokiy gosudarstvennyy universitet imeni M.V.. Lomonosovs,
(Furan)

FLU
j,-ffiuX.,- GAL 'BFRSHTAbl M.A.; SADOVAYA, N.K.
XJJRIJE
Chemistr;r of selenophene. Part 26t.Reactions of 2-ebloromethyl-
selenophene and its homologs. Zhur.ob.khim. 32 no,4:1301-1307
Ap 162. (MIRA 15:4)
1. Hoskovskiy gosudarstvennyy universitet iaeni M.V..Tomonosova.
(Selenophene)

YURIYKV Yu.K.: MZENTSOVAp N.Na; SAPOROVSKAYA, M.B,
Chemistry of selenophene. Part 37.- Synthesis of 5-(2'-seleaie.V:l)
pyrazoles substitutes in the position-3. Zhur.ob.khim. 32 no.5:
1444-1446 Vq 162. (MBA 15:5)
-1. Moskovskiy gosudarstvannyy universitat,
(Selenium compounds) (Pyranole)

TMIWVI YU.K.j HEZENTSOVAR N.N..; XLDAj,,B.I.
S~mthesis and reactions of 2-
Chemistry of selenoj*ienea ~Fart,'386
virqloelonaphena-*-----"4huriobkhim.- 32--naiW820-182
(MIM 1516)
1. Moskovskiy gowidarstvennyy universitat im. lf,,V.Iomonosovae -
(Selenophene)

YURIYEVO YU.N.; RMNKOP O.H.
f-ata3,vtic conversiow of beteroctclic compoundso Fart 58: Conversions
ne au2fidea. Zhur.
of 3-alkyltetrabydroppans to 3-d342Pen'tamethY,10
(MIRA 15:6)
ob,khim. 32 no.6-.2S22-r-19U Ze 162-..
1, 14oskovskiy goeudarstVenn" universitot im. HASIMMOSOva.
(Pyran) (Hathane)

ME tan R U-401M M p 14 TO. L"I"75zirt5ri-_i~~L~K~a:-_ni-ual~,~.--.IcirAom~----
Yu.K.; ZHIK(IARn.,A p V. No
NOVITSKIY2 K,-Yu- - YURIMJ,
curan with
awan series. Part 22: Reactioil of 2,,5-biS(Ghlorc-meth7l)
aminese Zhur*obolcliim* 32 no.6:MS24-1828 Te 162o ORA 15 -.6)
1. MoskovsIdY 90sudarst7emyy universitet im. H.V.Iomonosova.
(Amines)
(Furan

-EMOV, H.S.; PRIKAZCHIKOVA
L.P.
Stereoehemlstry of the oxnercum#on of dimethyl ester of ezo-cla-3.
6--andoxo-dLtetraLhydrophthftlio maid. - Zhuro'bAhim. 32 no.80V*"
2745 Ag 162, (MIRA 1519)
lo. hoskovokiy gosudarstvennyy universitat,
(Phthallic acid) (Mercuration) (Stereachemistry)

YURIYSV, Yu.K.; GALIMMHTAM, H.A.
--Ghemistry-.Of selenophene Part--39; -Condenzation-reactions
Of 2-chloromethyloolenophene. Zhur.obkhim..32 no.10:3249-3252
.0 162.
1. Moskovskiy gosudarstvenrqy universitat imeni
lf*V. Lomonosova.
(Selanophone)
(CouOnsation pwoducts (Chemista7))

YuRnv, Yu4K.; MAOISIYEVA, N.N.; TITOV, V.V.
Ch9mistry a pelenophons. Part 40: 'g-Diketones of the
selenophens aerieo. Zhur.ob.khim. 32 no.10:3252-3255 -
o 162, WIRA 15.11)
(SelAnophane) (Ketonell)

MOVITSKIYI K.Yu.; YURIYEV, Yu.K.; ZRINGARMA, -V-N-
Ftwan series. Part 23; Reaction of 2,5-bi5(cbIOrOr-th-.,I)
furan with metal cyanides. Zhuroob*khjm. 32 no.lo-.3303-3308-
0 162, (HIRA 15 ; 11)
1. Moskovskiy gosudarstvOnnyy universitet imeni
M.V. Lomonosova. (F~uran)
(AlknIIi, metal oYanides)

rJR*-YEV vu K GALIBERS11TAH, H.A.; RMANTSEV,, G.G.
Selenophene chemiatxr7. Part, 41; Zemai--n ef
2-ohloroviothylsolanapharle with amlm~ alcohou.
Zhur.ob.kh:Lm. 32 no.11:3562-3~67'.. N. 1,62. (HIM 115:11)
1. Moskovskdy gosudarstvennyy urdversitet imea
M.V. Lmonosova.
(Selenophone) (Alcohols)

yURsygy yu K.; GAIBFMHTAMp M. A.
Chemi gitry of selenopbene. Part 42t STnthdsls Of t8tramf06tf--
tutAd etbylanediamines of the-selanophene, series@ Zhur. ob.
kbim. 32 no.'39;3922-3925 D 162, (MIRA 16:1)
1. mogkovskiy goj3ud&xat7eniqy univaraltet imani M. V. &9=0807a-
(Stbylonediamins) (993.enophwne)

FEDINt E.I.; PETROVSKIY, P.V.~; REVENKO, 0.14.; YUR'yzV, Ju.K.
Nuclear magnetic resonance spectra of homologs of thLophane and
pentamethylene sulfide. Neftekhimlia 2 no.3:270-274 Ify-Je
1621. (MIRA 15:8)
1. Institut elemantoorganicheskikh soyedineniy AN SSSR i
Moskovskiy gosudarstvenniy universitet.
(Thiophene-Speotra.) (Thippyran-Spectra)

YURIYEVO r1494L ZEFIROV, H.S.
Furan series. Part 2'11: Wagner-Maerwain rearrangement in
3.6-andoxocyclohexane. Zhur.ob.khim. 32 no.3s773-782
bfr 162. (KRA 15:3)
(Norbornane) (Rearrangements)

U.N.; TITOTO V.V.; YURIYEV Y14AK PMHKMv VA
PEN AN; MAGDESHEVA, 0
Study of the disacclatiOn Of scme selenaphene-containing
A -dikatones using fte potentiometric method. Vest. Moak. un.
Ser. 2t Ehim. 18 no.3270-74 )tr .. JO 163. (mm 16:6)
1. Kafedra analiticheskoy khimii Moskovskogo universiteta.
(Ketone) (Potentiometric analysio)

YEFIMOV, I.P.; IAGUHOVA, b.D.; MAGDESIYEVA, M.N.; TITOV, V.V.; YURIYEV, Yu.K.;
PESHKOVA, V.M..
Determination of the acid dissociation constants ol. -diketones
of the selenophene series. Vest. Mosk. un. Ser. 2: tim. 18
no.5t49-53 S-0 163. (MMA 16 11)
1. Kafedra. analiticheskoy khimii Mookovskogo, universiteta.

A. F.
YuRtYF.V Yuo K-; OLEM"o
NOVITSKIYI 9 p
Furan serial' Fa~t 0~01b. khim. 33
,d rurf=yithiazolidineflo Zhur (141RA 16i1)
163.
1. moo kovaidy gosudarstvenW uuive,raitat imeni M. Vo
lawnosova.
(FurZU71AmIne) (ThlasolidIin*)

YURIYEV Yu.K.t GALIEMIITAM, M.A.
Chemistry of selenophene* Part 43s Reaction of 2-chlaromethyl-
and 2,5-dizathyl-3-chloromethyladlenophene with potassium
cyanide. Zhur.ob.khim. 33 no.2:462466 F 163. (MIRA 16:2)
1. Hookovskiy gosudarstvannyy universitet imeni M.V.L6monoaovoL.
(Selenophene) (Potassium cyanide)

YURIYE:V, Yu.K.; ZEFIROVp H.S.
3,6-Bndcxo-cyclohe%on" end -07010hexangs, Part 91 PM
Wagner,Meerw-ain rearrangement during the halogenation of
derivatives of 3*6-endo rolohexeneq, 3.6-emdoxo-tyclohexeneot
Zhur.ob.khim. 33 no-3.*8r-S':L3 mr 163o (MIRA 16:3)
_goSWar$tVennyy universitat imeni
Moskovskiy
I%V. Lomonosova.
(Cyclohexene) (Halogenation)
(Raturrangownto (Ghamiatry))

, N.S.; IVANOVA, R.A.
yURil&V yu.K.,l ZFFIROV
.
,6-Endoxo-cyClOhdkSU6a'and eyelohexenes- Part 9:
3
.
synthesis of awin6"aerivatives of the 3,6-endoxo-cyalohexane
:
(HIRA 16:3)
series. Zhur.ob;khim. 33 no.3:813-817 Mr 163-
1. Moskovskiy gasudarstvennyy-universitat imani
M.V. Lownosovas
(Cyclohaxons)
(Amino compounds)

UP
P" I "IN
8~ R 1.

~

3p6-ZWoxa-.oyalohaxaxw~ W4 -0yalohmnon, Tart 10i
Acetoxymarouption of dimothyl eater or--"*~- AV4:1
3,6-endoxo-.AA, -tetrahydrophthalic acid. Z Ahim.
33 no-3:818--820 Mr 163s (IMM 16:3)
11 Moskovskiy gosudarstvennyy universitat imeni M.V. Lomonosova.,
(Cyclohexoned icarb.oxylic acid)
(Mercuration,

N-N.. Timov, V-V.
Ap
Mir
Card 1/2

Card 2/2

NOVITSKIYP K.yu,; VdfjoVo V.P.; ILIDIA0 Yu.M.; YURIYEVs YU-K-
Furan- series. Part 25 Oxidative cleavage, of 215-cUsubsti tad furanso
(ICRA .16
no -1145-1 -AP-163*
Zhur.ob.khira. .4 U9
1, Yoskovskiy gosudarstvennyy universitet imeni H.V.Lomonosova.
(Furan) (Oxidation)

YMIYEV Yu.K.- ZEFIROVP N.S.; SHTEYiW, A.Au...
Furan series. Part 26: Relation between the rifttL,-,n of dlene
synthesis and oubstitu-t4on eAdition in the fursn series. Zh ob.
khini'O 33 no.4-.1150-4156AP 163. .(MIRL 16:
1. Moskovskiy gosudarstvanny-y universitet imeni, K.Unmonosova.
(Furan) (unsaturated compounds) (Substitution (Chemistry))

YURIYEV, Yu.K.; GALIBERSHTAM, M.A.
Chemistry of aeleni)plhene. Part 45, 5-Halo-2-chloi-east-n~-Iselenonhangs.
Zhur.ob.khim. 33 no.6s1780-1793 Je '63. (HM 160)
1. Moakovskiy goaudarstyennyy univeraitet iman'A, M.Lomononova.
(Selenophena)

YURIYEV, Yu.K., ZEFIROV N.S.; PRIKAZCHIEOVA, L.P.
3,6-Endoxocyclohexamea and -ejolohexones. Part 11:
Cirs-hydr,o;qmercuration of dimethyl eater of
exo-cis-V-endoxo-~e -tetrahydrophthalic acid. Zhur.ob.k)lim.
33 no.6tl!t'93-1801 ~Je 163. (AURA 16-7)
1. Moskovskiy gosudarstvennyy universitat imeni M.V.Lomonosova.
(Cyclohexenedicarboxylic acid) (Mercuration) (Stereochemistry)

ZSFIROVP N.S.; YUR'YEV# Yu.K.; PRIKA2)OHI.KOVA, I.P.; BYKHOVSKAYA, M.Sh.
3;6-Sndoxo-cvclol-.exanes and -cycloh~Xenes. Part 12: Stereo&4-aiStry
of nucleophilic addition on a GZG bond in the aystems of
3,6-endoxo-cyclohexe.ae and 3,6-endoxo-eyelohexadiene. Zhur.ob.khim.
33 no.7:2153-2158 11 163. NIRA 16:8)
(Cyclohexe,ne) (Cyclohexadiene) (Stereochomistry)

YM YEV. )M-Kti. MAGVESIYEVA, N.N.; TITOV V.V.
Chemistry of seleno1*9ne. Part 46: Reaction of
(A), -4,ensoyl-2-acetoselenophene with hydroxylamine. Zhur.ob.khim.
33 no.W2158-2163 J.1 163. (MRA 16:8)
1. Moskovskiy gosudaris.tvennyy universitet im. M.V.Lcmonosova.
(Selenophene) (Hydroxylamine)

POVITSKITY K.Tu.; YUR"YEV, 33t.K.; ZHINGARSVA, V.1j.; YMSoVf M. S.
Furan. series. Part 2,04 Synthesis of 1*5-bia(A-dialkylaminoethyl)
furans. Zhiwlob.kbim. 33 no.7~,a64-2167 Jl 163s (MIRA 16:81'
1. Moskovskiy gosudar,stvennyy universitet imeni M.V.Lomonosova.
(I~Itwan)

YURIYEV, Yu.K.; MAGDESIYEVA, N.,N.;-TITOV, V.V.,
Synthesis of W -(p-nit:robenzoyl)-2-acetoselenophr--ne. ZI-AU.-.
ob.-k-him. 33 no.8:2577.-2578 Ag ~163. (MIRA 16:11)
1. Maskovskiy gosudars-tvennyy universitet imeni M.V. Lomonosova,

YURIYFIV, Yu.K.; MAODFSIYEVA, N,N.; BRYSOVA, V,P,.
Chmdstry.of.-selenophene. Part 47-..Synthesi.-i arA alkylat-ion of
t'3 -diketones-of-the selenophene-series. Zhur..ob. khim. 33
no.g-.2579-2581.Ag- 163116 (KMA i6tll)
1. Moskovskiy gosudare.tvennyy universitet imeni M.V. Lomonosova.

ZPFRW N.a.; IVA NOVA, R*Ao.; KECHMs #,~H*;
Bromination of addWits Of 2-mtbYl- and 2.5-dimthylfuran
vith maleic whydrMe. Zhur,ob-kbiTne 33 noolO.-3439-3440
0 t63* (141RA 16:12)
1. Moskovskiy gosudarstvannyy universitat.

MFIROTO NA.1 IVANOVA, R.A.; FIIXTOVA. R.S.; YURIYEV
Deamination of methyl oster of exo-cis-2-amiw~-3.6-endojco-
..hezahydrophthalic acid* Mur.obekhim. 33 no.10:3440-,A44
0 163. (141RA 16:U)
1. 14oskovskiy gosudarstvennyy universiteta

ZEFIROV N.S.; PRIKAZCHIKOVA, L.P.; BONDAREVA, M.A.; YURIYEV, Yu.K.
Hydroxymercuration of dir4thyl eater of ezo-l-irethoV-3.,6-endozo-
e-trans-tetrahyd:rophthalic acid. Zhur.ob.khim. 33 no.12:4026-
4027 D 63. (MIRA 170)
1. 1-loskovskiy gosudarstvennyy universitet imenj Lo-monosova,

ZEFIROVj N.S.; PRIKAZCHIKOVA, L.P.;
--Stereachemistr7, of- the addition-.of-mrCury lums -to olefins,
atudied_b~-tha us'e-oflho meroury salt of-trinitromothane,
Dokl. All SSSR 152, no.4t869-VI 0; '(53. (miRA 16:11)
1. Mookovskly gosudarstvennyy universitet im, N,T. Lomonosova,
Fredstavleno akademikom AA Neismeyanovym.

of 1-y- i oV r'l-c~.h,lf-,~-rimr,~.'I-,'fl",,[, c,, r0 1', Qr..
I yan h 1% -1
r g,

-if 7u v G'T IrEFS!"I'AM M.A.; I,
Kinatic sturly' -ill T,*---) 6erles !'-f e - - n r--,T.- b e r e d n (I a
-, . I I I ~ -1 _.PoL
Part 2: Kir.etics of soljolysljo of find 2,5-lizethyll-3-
chloromethyl comnpciund3 Of fUranp tniophene, grid selenoph(ne in methyl
alcohol. Izv. vy.~j. uchob. khiia. j. kh-Un. tek-n. 7 no-4:598-602
16,, 33-12)
1. Kafedra arganic~esRio-,:- ~ _~j 4 "o-skovskogn, -,3sddaz%Avennu=o univer-
'teT
L a
s

YURIYE-Vx y~k.K.; SADOVAYA, N.K.; GREKOVA, Ye.A.
Chemistry of selenopherie. Part 49: Reactions of 3-bromoselenophene.
Zhur, ob. khim. 31+ no., 3:847-851 Mr 164. (MIRA 17:6)
1. Moskovskiy gosudarsl;vennyy universitet imeni M.V.Lomonosova.

ZEFIROV, N.S.; DAVYDOVA, A.Fi; YURIYEV, Yu-.K.
Cis-bromination of dimx!thyl ester of 3,' endoxrdihyd.-cpht alic
th -
acid. Zhlir. ob. khim. 34 no. 5:1681 Mj 164. (MIRA 17:7)
14oskovskiy gosudarstvennyy universitet imeni Lomonosova.

YURIYEV, Yu.K.; SADUVAYA, N. K.
Chemlstry of selenolphene. Part rjl*. Sulfonation of
and 2-methylselenoplaene. Zhur, ob. Khim. 34 no.6sIS03-1807
Je 164. (MTJIA irl. 7)
1. Moskovskiy gosu&irstvennyy universitat Imeni Lomonosova.

NOVIT~.IIXI-Y, K. Yu,; KHAGHATUROVA~ G. T.; YUHY%Vo K.
FDran series, Part .112; t-jp- s7n-Uls-ais
of 5-,nitrt>-2.:-f~arfLr~rl.am,tnes, ',hur. ob. Khjm. 31, no.6zTlUWaat
I k~ Iw~
Je '64.
2. Mo~ikovulkty gosudarstvermly univaraivt1%. lmaW Lomononon.

YURIYZV,.Yu.K.,, SADOVAYA.,,.N*Ke
Chemistry of salwophene. Paxt 529Sul-ftaatlr-,n of iselenophenew-
2-aldebyde and ofilenophene-2-iarbor7lic aald, Zhur. ob, khim.
34 no.7e2lc)O--219,'; Ji 26~1, (MU 17:8)
Imenl,

MEFIROV, N.S.; FILATOVA, R.S.,- MWYEV, Yu.Ke
Beha7dor of dimt; 'hyl enst,~-r oe ~~twvmo-3,6-endtAohearahydra-
phthalio aoid In solGiolysia. Zhur. ob. khim. 34 no.7t
2468-2469 Tl- 'C"i4p (MIR& 17ag)
1. lftakovskiy goaudaratireninyl universitet imeni I-l.V,T=cnosova,

k SM-0 IWWA
NOVITSKIY, K.Yu.; YURIYEV:, Yu.K.; ZRINGAREVA, V.N.; GRMLt, Kh.
Furan series* Pltrt,33.- Reaction of 3,4,-.bio(halomethyl) furans
with metal cyan!Ldes. Zhur. ob. khim. 34 no.8:256&2570 Ag 164.
(MIRJA 17:9)
1. Moskovskiy gosudarstvennyy universitet im. Lomonosava.

YURIM, Yu.K.; OLLIBERISHTAM, M.A.; KANDROR~ I-I-
Cleavap of di (2--thier7l)~- (2-!:elmyl) lead imder Une effect of
hydrogen ehlor-Ids. Zbur. i b, khim. 34 no,12:4116 D 164
1. Monkovskiy gosudarstvennyy universitat imani M.V.tomcnosova.

ZEFTMV 11. S FIA 1 4,01'. A. : IIJR I YEV , 'iu.K.
Ea- 1-7: ~:-,.ff.gura
of the adducts of 2-meth-%rl- and wf-
yTiride and 'heir epoxydation. ?h-ur. ob. ki-Am. 35 no.!..,-*,C--,-,
anh, u
I JA~ T~rjA
Ja '65. 11 - 18:2)
1. lL4cskc-,v2kiy

11111 !7N, Yii.?,. 14P41"ESIYEVA '10HAMOVA A.T.
Chamistr,v of se' noLhen;7-. ',-art 53:
Zhur. ch. kh 3 5 1 F -70 J a 5.
1. I-,Iookovsld.y gosudarstiemyy un--versltet.

ZEFIROVp N.S.; KANTAMS-KAS, P.P.; BAZANOVAp V.N.; YURIYEV, YU-K.
Stereochemisfry of the nitrosochlorination of 2,3-dicarbom-ethorr-
7-oxabicyclo-(',1,2,1]-5-heptene. Zhur. ob. khlm. 35 no.4.-752-753
Ap 165. OKIRA 1835:1
1, Moskovskiy 110oudarstvannyy universitat im. V,M. Lomonooova,

ZEFIROVO N.S.; PRIKANHIKOVA, L.P4; YLTRIYEV, YU.K.
3,6-endozoeycle5hexaneu and -cyclohexcnea-, Part 20: Acetozymercu-
ration of demethyl ester of 3,6---andoxodibydrophthalic aciLd. rhur,
ob. khim. 35 no.4:639-641 Ap 165.
(141RA 18'.-
1. Moskovskiy gosudarstvennyy universitet Am. M.V. Lomonosova.

TRESHCHOVA., Ye.G,; EKKHARDT, D.; YURIYEV.
Correlations in the spectra of furran, thiophene, and salenoi:hene
derivatIves. Zhur. fiz. k1lim. 38 no.2.295-303 F '61,.
(MIRA 17.8)
1. Moskevskiy gosudar.3tvennyy univeraltet,,
MW

Y-a.,,iy Kom~ltaritinovich; GOL'D-EINMRG~1 f".S., red.
[I.acoratcry work in orr-ar;
raboty po orgarachaskoi khi,..,ii. lzi-vo ~"OnK.
univ. No.3. lzd.2. 19U. 25"1 ('-,l I R A II

YURIYEV, Yuriy Konstantinovich; GOLIDENBERG, G.S.0 red.
[Laboratory work in organic chenmisti7j Frak"Ichesk-le
raboty po orgunichaikoi khimii. Moskva$ lzd-vo Mosk.
univ. Nos.l-,':,. Izd.3. 1964. 418 P. (MIRA 18:3)

D W-ILOV S-11-z gIJav. ;rej., ZAK~ARUVA, A. I. red ARBUZOV 9 A- Ye.
d, . red.;
red., IKO
KAVER21"EM Ye red.; Lursm
red IUSHGHRMKO~ K.P,,, red,*,; ITEWISEV, 1,,,,S.,.red*-j
RbV, A.A,., r e, -1 z FREYDLIHA H.,Kh... reC;, SM-ff AKIN,
PET
rad,-. YURVY15V Yu.K.p red,
red.. HCHU KARBY S.
of_ oi,ganic syntho:As) Problemy organicii6skogo
----323
sinteza. Vlopkvaq Naului., .1965.

I. jyu.; YURIYE VYu.K.; OIEYNIK, A.F.; RODINA, N.B.
NOVITSKIYl
Furan series. Part 34: 13ynthasis based on (I -(2-furyl) ethylwaine.
I Z-jur. org. khim. 1 no.1:160-162 Ja 165. (MIRA 18:5)
-rosudarstvennyy universitet imeni M.Lomonosova.
L- mcako,v's"kiy

YUR I YEIV Yxt.K.; MAGDESIYEVA, N.N.; TITOV, V.V.
Chemistry of selenGphene. Part 914: Reactions of' 4.; -ace tyl-2-ace tose lenephene
and the syntheslE~ of 4,J-hydro-xytei~~zryl)-2-aestoselenopliene. 27hur. org. khim.
-1 no.121.63-107 Ja 165- (MIRA 1825)
1, 146skovskiy gosudarstvenny~, universit-et im. N.V.Lemonosova.

NO.VIAP.,Kly, K.Yu.; YURIYEV Yl. - OUL-INhi, A.F.; D-0,11ISOVA, G.V.
. -I(- I
Furan ser-leg. Part 35: -Izm-theoe3 tared on 5-me4shyl-2-brrrioace*.,7)LUran,
Z,hur.,)rg.khim. 1 no.2086-388 F 165.
(KIIIA 18:1,)
1. Mookovskiy gosudarstvenny-.f universitet imeni M.V.Lomonosova,

NOVITSKIY K. Yu.; GRESL', Kh,;
Furan series. Part 36: Lffect of the solvent on the reaction of
2-chl-oromethyl-furan with sodi= cyanide, Zhur,org.khim. 1 no.3:
539-541 Yx 165o (MIRA 18:4)
1. Moskovskiy gosudarstvennyy universitet,

NOVITSKIYO K.Yu.; OLEYNIK2 A.F.; NAYDENOVA, N.M.; 1-URIfEv, YU.K.
Furan series. Part 371. Reactions of 2-vinylfuran oxide stilth ammonia
and amines. Zhur.org.khim. 1 no,38541-5.1,5 Mr 165.
(MIRA 1884)
Moskovskiy gosudarsbvennyy universitet,

r
54-i.442:547.266
A' ye v - il
n t a n. rig

a
-I.s .ibs t. i t ut e-I pyr
if
mell
y'llr
3UB CODE
A'I'D PRF'3,q Cl 4017

V V DISTROV, V.F.- LEZINA, V,PO' YUR'IBV, Yu.K.
Stru!Aure of f-and b.lu- fi-dilketires of tte zelerxphere- ceries.
Zhur. struk. khlz. n,:,.3:402-406 Fa--Ta 165,,
(MIRA 1818)
1. Mbskovakiy gosudarstvannyy universitst imani M.V.Ixjmonosova i
Institut khimichaskoy fiziki AN SSSR.

YUR IYEV Yu.K6; GALI&,'HSIITAMv M.A.; PHOKOFIYLVA,, A,F,
Kinetic study in the series of five-memberad heterocyclic
compoundc of arcmatic nature. Part 3. Tzv. v7s. ucheb. zav,;
kbim. i khim. tekh. 8 no*3,.421-,425 165, (HTRk 18:10)
1. Moskovskiy gosudargtvenn-yy universitet imeni Lomonosova,
kafedra organicheskoy khimiio