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

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001963220013-4
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 19, 2001
• Sequence Number: 13
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

lato the
Coffir"VORM 11~ and 0-atkylpfffolilliatif, XXV1, vu,
x ~ vilf'ov aftil 1, 1-i (4119(fliv (Lotnol-Ov State utily.,
Zk4at:, zk*r. 14A." Kkiffe. (), Goen. Chortu.) 20.
171-4([WO). cf. C,A. 44. 1411tZI. 44,14ib.-Alkyltim4ni.
dius (fetrohydrufurati-A) wrfr com-itcIl to the tw. lit, (U.", 1.
pandt" AlkylpyIrWiltitics (1) toy Iffulljoing thcon (is "
179 SKI
vii"finin.) in oltrong Mls streatu hift) an AJA-filk-d
wijf~ *1 3.110% The
; frr%h orvital"t VsAt isolord fm rach run. t
boo,wifid I .4tv ItewriforIf: a-Me (;Nil", from J.pNfjk)4.
lot" 11V-1 3'. It- ONNO. ovif JAMI IftFale,
lit M1,;A,*6,,, 1:11", 10-KA710, ati-
i -SM" (picram, ni, 103 -
-Jr (15- 1581, dr
iiiiiiiiiiiials,

dW vM tmmmk gild widt hyd e! Wdife. Catirk
ft (is-2-buted*-1.4 . Vu. K. Var ir
Tz
1. ' K it . and R. K. Bfice
State Uttiv., oscow). Zhur. ("id Khim. 4). Cen.
Chem.) ZO. 744-9000). cf. C,A. 43, A(1113f--Nv~4ge a(
(iCCUOU)s (9) at (V-N dn"Anin. in %(rmr AMh Rt
400' rAire mtwh C, omw CsIl,, 110. aml Ir44v4 0 futam
(detected qwifitzitivety). At 350, 1 gave C.11'. detected,
as (ClIFIrds by Absomtkat in or-CHCI.. I (Iff 9.)
Mated A4 00" OVVr akffttOgilk~Att! CUtAlySt At d Off(It"
mitt. with conrumut %mm"ge Of MIS. pire 0.3 41.75 6,
jft.wr,,k, t&-- max. *td beinc o(itakwd at 4(Wl'; the uw 4,1
a lips attu. at 3NI, over Alto, simituly CA%V a trAre 4
lkiap*rgir, i4rLd ist 400'45j. was obtained. flydrogenA-
14M of I oy" Rarity NI In PtOll pvv W.31.
IfInF4,44w, (% 115-164, alif LOU ' d:4 lAvvj; tW4
(141 gjImated with 2 g. ahtmogilicate walyst its 11Y0 -,#I-
pvc 4 C.. nowq. ilklittate. yiet4log on dion. My
bm
w it h Rr in CCI# with %tristig cooling 9mve T,4-4t6fmRv(,F(r,j
hefffurom. INI WLI$~ 1.4" mil, IMILM), d"' 21,414, white.
t c rtmalluter ol the csitllyrtile yk+14,41 ZV'
01`010, Nit 1491 2'.. Ili? 1434U. ill's RKII H,#mh,m-PW4
&W, M. IkIl. K(KAgAIAO

coornpatrative Feactivity of Ammilaiiii isad andine in feection
with (UM t4d(ISTIL1111dine. XXV111.
Stair I niv. /4mf. 11h.h(kel sollit." (.1t
ClictitJ ~0"IWA AW-741). of- 1.4"m
t nit - in# 11 V. I.,,Ht 1-, 4 1 No, 74, NI, h,f, Li.,
CA 44,,MW I to fill, 1o,0111 Ili thi'l 1"1114 11111k V
fillol PlINII, lit
\11. al"I MINIt, twild, milt, I mid mk
flat. ~, lot I'll IA, 1,11:f j it, ph,ft t lift It
41-1 #4 -4
41 llilk~jtl Hot #OfftO blo: IN 44
lo-ov (UhNifir, Ille W.101"wk 'Alic Ifitfiliffitil lit to liffool
-.-t Ale If ill 140 No' with thir valk-eg 4 itiv foired X
llrli%4 (tit p* 1141%. Viorlifif (if IS Z"I";. off 111161VIA14A
1-foOtivu. %liv C.11(aillvd, ITA"JoYlpt".4r, h. Ill A". m-
tit 1!-j IN 1103 It', ofli' I it:"
I . I 11 62. PA,4- fit- 0 NN I I A 11, A,* t A 1 -4 0, 1 is A S .11, Alto m
1141' jv~-tldv xt%kq .6 mioll. III MI. I1 thAmy) 'Atid
N111 iiil",! i%itl,iliol I, t0th It In- IIWtI If" Ille
PlIMIXII, Ali.[ fiff.4111.1111" KA- .4
1'. ~*Jf it". ...A Iq pf-b"I

afivitiso tit conum[A mad dfUltwo ta
=wts 0 Will r
with fusto 410 fulan4finv. Mill VII K,
Vill*" I %1 1, klallorl"w'i -1. (.'r"
c.~,-.s,T,." S-N 10, UMA tk Ill"AI)i Fudl. 1t,401-1,11 I-0, Sr,
C., 1. 43. UW l6, H. %I

PlIf4tittlad Of 1.4-diruthyLtumn by pyrdytis of stultme.
Va. K. 'k'ujr*cv, G. Vi. Kutuhrmma. au-I S, N. Prif"V
(U."V: Viimopowv State VlAv., Nlowim). Pekbuly.fkaJ.
Xag* S.S.S.R. 72, =-60MAJ).-Mcsityl 036W With Cl
SQj( in AeO (Exontaxii and Gallup, C.A. 42, X1114L
save 4517a of tht imUms. m. W*, S g, of which, dry-distil.
with 20 K. rao. M G. CUO, 10 g. Fe filingt'and UZI C. Phs-
Nil, mvA the diAtiltmir washed with 2 N XxIfIAN,
and 11,0. iraw 7d'7c 2.4-dimetA34furao. tno 14 '. xj: 1.437.1.
d'O 0.14093; vrilh pultric mthydride it yi6ds the a4duct,
419kYJfPJf. W
75*(frt=VtP).ilccorup.IfW)&~ It thedisift. above is dmir
enly with CaO-,N'gtCO#. with solW NaOll. or with 441t-j,
Saoll only.SfeCID (40-5,570) is obtaitird ard no iur~;
dttiv.

1h.,
.4 11=0M VMU,
.3tate VOW. 114 y AM. Nank S.S S.M.
(50 C.) ovet
[,that 2,kJ* at 10 in it Na(M. CATV MUCh If,% Xn4t 4
cAtAlyrAte, which an ditu. with F,100 gave 0.3 g. solicl. m.
_-4', Anti MUCh C; VW Off-CAI CGOtaft[Cd MUCh f( And
Ittins. A similair eipt. with 25 g. sulfide, tun in a H~S AtM.
aye SO g, cstAlytatc that solidifittl an itandisig and. on
istn.. tn. 76.5-7.5' (fr*= pyridine), tome 0.6 c. pure
A
roduct, thus obtaiined was z,2.di!Aio(av_e. confirmed by
naly%is,mol. wt-o and ceoversion to 1,S-prm4p4xcdi1hi4J,
.1 17 V, tot* ~,SM. dt, 10770 upon beating 16 hn.
." RUA tok it.-A. t9e d;"I" M. 55.5-d.S* (from
1 1, was idvot" with an authentic vivrinwn. ttrpcti.
14111 A l1w %yothrill it XWl* wilh to) g. stdrillf give 2 It.
dilh6,14ifw, lso- A A)- 1(41*1 In, " 11 IV, TUC pf.hluct (Ail.
to give reactkinscharactettok. of in"Ptatt%or sutfuics.
G, It. Kowlapoff

CA
Reaction of tothytento loside and ethylette glycol with &tit
Mania at elevotted fealferatum in tfw presence of Aluminum
%'it, Nmif,kif, awl V. 1.
StAtO V(414,
Alkhaily Mad. Sauk ,;,SSR 74. 47.1"XIS041) -Wo1v
'thylelle (11itle (1) will \11, ill-ttiv jal-wmv .4 .1*1,4 I.M It ll
PW WC fVIXW ICA 10 Yi0if IlVli4llllr MIA till 1110114 It, llt~ i %141fti- %v
Ait will Mmycmov, C.A. 42. 1.160) jaid A4 11 Aml -.% III
over -AIA At 42~1* Tichl alkylArett lllk"tlr~f.
4"t of the rv-Aetim tof I with Nil, .)%t:r AIP, it Of' g..t,,
11141AIMN (hAt tvily Ilythlille fol"futt"K, Gwill, Amf 11.1
"Y" ",e I'll 'to it-tMot illmmos lite pflktiiv(~; Ow
11 by i*giK-ri"t4"i a I iwo Avil Nl,,axv
Nils at 41m)* over AN' I. cA % v J53 g - r.4 i.-I-
vmte firms 3W C. 1; -11 t. Aell-Nih,
tit, 97', Atut milled '21- ,,tul 4-mthyfliV6011- 04volifil'il
'1111-f ruell-Livi, (mortilI414(illu will fitillit'r vlv~lli I tit the
j-kr-4Iv,l 48ad Aft114111911 A fli-44-14111 Is 11:1 17 '
*a- offNifflA. it WAN not pvtWiliv. 1#414 .4 moh- flilki .4 Ow
01A) Ito (A fit N,*11,4ivv-r A1411l At 4filf, C,t%e,
frinot 27#5 g. giyewil. 276 S. lrAtAtysme Out viihteil, I lg~
Aell-NII, mid isilied 2. Atid 41-nie1hyllivristin", hiettlifivit
liq ablivr: 114. lywridine wall dirtrefir'l. 4.. M.

YURInTs YU. K... KONDRATIRTA, G. YA.,- DEUENIEVA, A. A.
Awanidines
Simultaneous catalytic dehydration of 2. 5-dlalkyland 2p 2, 3# 5-tatmalky1furanidinas
with hydrogen sulfide. Uch. zap. Moak. un., No. 132, 1950.
Monthl Ust,of Dissian Accessionsp Library of Congress, October 1952 UNCLASSIFIED.

f6111 VA,t
Pyrrolidones
Transf cm, ation of buttyrolactone into oe-pyrrolidone avd, pheryi- 4-p-yrrolidGne, Uch. zap.
14osk. un., No. 132, 1950.
Monthly List of Russian Accessions, Library of Congress, October 195V Unclassified.
- - ----- --- --- -

r S. Karuk*va
&
;t wv 71W.
13 mi, H-140s (d. 1.15) to 10 C. I-ph=jfpycrw"n(
tal. AcOH at -2V kWs to an wive = .01ma".0
addaAmompkte, after suadjac oftniot the ooLrj.VjMs
at.
(M), kmp. OW dowwr addet. (OD mho. Imccad
of lo minj 91 ;idd*. (Lavalic, ast. if", 41.
M). Itive 41 17=6 -84 (Of the pcodmt.)-_)UdAhqtiaci
ficl P-T-e- the 'Joak,
whicb witb I&Off
yu a-W41WOC, M, FAOH).
TV the rl SO &rir'. kawed as (to Hof a&. as. fig* (ftom
"*- sto 1). which With 4&4U calve the frcs km. Loa,
(from FJO). - The bea " (90%) is oWiaed With-10.5", U b St.0 [a a N atm. with 84 c. "r desiv. lm EW m
Or mM 40 ml. AcOlf as sdrent wben a4da. uims 10 ML,q;t! ftxiac 2 brf.. am gutftinco" ~kr
hi&tbw or krwer tempL gim kiwer
yidds. the formt.
Ykkfiac omm di-Or &dv. kb is dUkmft to up, Tnat-
#-Be
0v Im Rio Wkh a sou. of
If-VO~ Imm 0.3 9. -VS.V(X. 0 ML H.O. and. am
amt. of MCI hurnmLittly YCEIM
NO* 4*40G m.- 100". idtmtvrb ahm
mm. Aw-. cl 9 C P-Sr deriv. in IW ml. EW t* a sofa.
09fluMcoac-5.8c. ft-U(brtfu-ati*n)fm2SmJ.&jO)Ju&
V 4100, vW ntfudug 5 bmgt- upon p"ripc the mfxt. OR
add, 0. 270, (doom
Id 17% *a an (Mt["

YURIYEV, Tu.K.; MRSAKOVA. I.S.; ARBATSKIY, A*V.
Nitration, bromimtlon and carbox7lation of 11-phen7lipyrrolidine.
Izv.Akad,nauk SSSR; Khim*otd. no.2:166-171 Mar-Apr 51. (GUG 20;7)
1. laboratory of Orgwdc Chonlatry imeni 11-Do Zolinak-i.7 of Moccow
State University.

YURIYEV, Yu.X.; ITOVITSKIY, K.Ta.; LL-4-MOV, L.G.
Obt-14ning of monoethanolarylamines from the et-hylene anl-
oxide. Izv.A7zcad.najk.SSS.TI;Y-him.otd. no.3:317-327 1951-
((;LML 2-0-9)
1. Laboratory of Orr nic Chemistry imeni IT.D. Zelinskiy of Moscow
State Univer3ity.

I IPM El:i~-T.~.-~ullmllqarjn�2kr4npc3lwll3p.
A"d*Wdm MW DmffijwA ztuddcL Va. E:.
Yttr'cv wd Lt. V4. Lavias. Mar, ObAckjKjj4L (I. Cm.
Q30'-HiO9rVhT- with PwtfaR Ad
SumnLIU7 d scitam work (943 cd~~)
0. U.

1/0
I 191440. 111CM (41 I:dl ' kll f(HAnithlir iAt 444l') gi,l-tv,il ovff
All; dinkc gave 4 t,4,0 44 ft)VF010 jqnAI, 104t) (Ar Pyrfolain',
1"11. Riniction of nifffio Pytomattilte Withs taulAst. XXX
Vis. K, Vtu'ev And U. G, Wwfel'thlrin, 164, V444-
14*11ANWC Of (MM Ind futilsild(ne wids mots 04 stAdifts PavAte of 9 C. US Vist'viff, W r4-61,. ltia 1,41173. dl,
.
ststid divilded. X3UX. Yn~ K~ Vor'tv atilt V. A. TttmovA 1.17KI, atul U c. PlaN
1t, over AflOt Ili A N Ortam at 47V
(M(P4cu* male UnIv.). Kkissf. (I. Gen. CAVC 14 V.. PbiNllt arul 1.5 c. (17,1'~) 1-f-kessylpr7d4l (1). tn
Chent., 21. & (Wessyle Zapiski Mvs4-ev. 58". At 400' the yicht iq 35c, while at Min 2217.. 1.%
f;0ss,d,j,,t- Cniv. 79. IUS(UHS); C.A. 4S, MEM.-FUrAll UiOM. ak)aC With 4klxxlt 14"o furml of a I atioUr ratio of
and furAniduir heat"I with sulillle,% or Amid" of metak PhNilt is uwd, IleAtnig I it evl" with *1 C, J-hNII, Aro
tilt not etchAncr their 0 for S or Nit. Thust, pyrites. Fe.6;4. 11,3 g. xxtivalctl AIP, in A ~rafril tutte S hr%. in 3511" j~svr
FrS, AMR,, at 3'.15-410* (Ail to *Ill any fratts 0.2 g, 1. [tilt tit 31W. M7, .1 fwail,alt,kie. tit 1-.W. . ..
elth" which are retruvrted rr- ..M.Aiticli; At _V41, A~ ..t 1!2il" 111c Vt. 1.1 WA~ IN H,
Mvrlk~, .1fliendifix ("I t4mililkstiq Iticld): the decontpii. dissittig I0 C. r4ter. 27, g, PhNih. amf I g. A1,4 1, ill, if
1911" 94ve PhNilt, 4 IlAt" 44 1. Alld *#IV; 2-1111,111411111&
UMC 1110WIVI! 411 2 IilttS *team At Jtk~-44W avre AI,44~ if AL.Ch it untitted no rr-i,:ltlOi mxuri. Px-~#Jcv Of Ill K
CAWO up to 3,21.5% Ikeoplusise, bris "4,* 1.5050, 11!, tter ever Alot in a Nawi.At 3,141" gave COs~ W9 it. fut_)lt~
.111.1 1 C. unclunipA "ter: (he rtcr i~ tiliChAnat-il "I Iket,11C.,
-.% vr lCIAts Its A N attu~ At 3-10)" (a lri~ 4 CO, kirmu, Pimm
mi-I IlhNAI, psv-inl ovrr AM), ut.& N,tlut. *1 440)"
1: tw1we the %Ic'LhC grisl4l, tit 1..it~ifj 2 If-daUl"
4 sit, nuclear to, Reacei'm of methyt (licraftildsw
W atillialts, XXXI, 164, ~111 7.
41144, It% of IM, g tie
10vto I'll 411" 1 - M,, i ,
1,144 (fift) And 2" It. 1111,4111, ul 44 N,
Milt, ker A11(hAt 3illi ii.tvt- 0 1,, 14 jg~ 111tNII, tilt t.5 K.
b, 101 5", Ril` L.,J,441. 4:* 1.01161;
PAOSICt Of Itle tte- at :Pit)' OW
ill A N Alm. care 420g. properle. anti MeOlf, fly-Int!"k of
the "ter wish 21 N N`A0If 1 h4", At rittItsig g;&vr 7d% fife
i.sid. a qrupy atkril" I, m4tis,. this tivitett tit Vu-itit'
begifts; tit kPic C(h. Whicto oc"A" (rerly at 300-P. wicllfiot
fulismidixis, tPu C-S". stif IMM, (1:* WOW G. M. K.

Yul"! MIJ
by Yu. Ir', Yur I ev, cl,1.4 E. G.
The reaction of met'71 furoat'o uiith an-ilble.
Vendell slmeln. (i:..255)
SO: Jow-,al of GenerO, Chqmi,~,try (Zhurnal Obzhchei rhirml) 1951, Volme 21, 71,11o. 2-

yu,,r-','Ev, Yu. K.
Ul bi K. ev
th anilLn 4
rfrie react-I on of -,;et!Vl:',etralVdrO'
e n .
E. G. Vendell olnt L
ev -trr Obshchei Khirdl) 1951, Vol
SO: Jouj-j~aj of General Ch e 21, ilo. 2

Vw K. R- Vol,
l.ifwr.pv (ACUMW-14f v UffivA 11:0,11, Ak-ij,
N-took.4 S-S~R..Ikbl. Khiac Nat%& 1951. 317-2 .-Taimste
(44 it.) 600 VOI or I'to\'ff. xtvl .1.1 old
IIA) M I I -14V ill .1 4 Ill,*. (at Its, vu-I 44 lite lite
loollp. fj~ ns"oolust"VU-4v lot 70 PW Its qtMe 4 fill. V-411
Uillst ~Ilpt vis-1,14 Zs A"V, M.Wit'llot *11.1 oil. 1-4. Got'.
not. xv 1.101-% rf~ralr. to. 11.4* ((""CA V will.
riptin Ames, "Ill U."I. the Yield dro-lit* Ill 32%
Stlorlitid ot,we not appe-at to Atfoovt lite view, Millillulv. P.
!f4uhilitent 141 Ill' its Ow form"m of Z0170 (Ily 'XIA 4.111,41
clirrio k1%. to, IWO, ;it., W
04fale. Ii. Post): o4foromw 140% ott,"
to mi. M01f, and 10 mi. IfO ticated with it C. I afler
inhial b"Ong an a steam halb kave 70 A No" I-C.!I,NII-
01.01.411f, 111 1929, to, 501 (piridlp.m. liiol"T~ e-AtlW4l;iip
Itn'tror Ilse ststwo Of"Wid'itle give 1411,;o f- Met ICtlNtff-tl,
Ot-I'll blot MI 1* sli,* I.AW, I:q 1,1,1101 -~lhf ill.,
I ~4.~wrp 1`7061"), to. 1XV, lot 4 1'.

19
chlorwillu axidlr G~ sluallauto oxide Oil 4e caulyff la
XXXII. Vt*. k Vt81*.v'A'Vt
V. A - Tlwarv.4 (Sk-ow N;ife I 'sdvj._ ZA~, ' -(*-A. 1,1
Kht". (I. ("fli. chims') Z1. 742 WIPM); cf, Ifka. Afeum.
I he Ot)!ilt111M trM IL 0( tr;Al1Af0fMA1I4rH OffiNFORidiffe (1) IWO
P~'Prlkfimr (W) w Wopkatte (111) ties lictow IhAl (if 4itnihir
.0~climi over AIA al-we, Inst the yirlls nf 11 and III are
the (ortnAtia"
.wvrrelv l"himl. In the prcwft~v of Cr4_
411 It fW10 1.41 3,10 !1116' 1* XIN"HjMnieli 11V tlChVdf0VttAtlOn.
at 'Am) . The Law limbal,tv forms from pytfOr orat either
hill"'16-11f. nt (urall adifig fr(Ists 1. which
met CON A1,41. at NO% l',e*ajxr of I twer Or sistdvo
(9.5 33A% 0,40 In a NIto stfraill at Mol UP* al 4; 4"
tr4dily Kate 11, pyll-40. mold 4..411-41440; fhe
f0fMAII-111 44 It 0111WAIS I'VC-21 lit MW With all VAIA4410, I"It
ski the temp. 6 raiwJ to 5101 lhe mint. lit It dedines rAphily
W 0. 'Ahilt- the VIC141 Of CatNIOle fj," With ift4WASM Moil,
and that of pyrrote Is lxnt sit atmt 010. The b"t cuta-
No compal. 14 1r# the higher range a(CrA ontim 1.
The ma%. yield (if It I't but 18% of .01-44' (with AIA
it frAdlex at 350, and 44.A% lit 400'), Pure
wt? 1.44.31, d!- nMI: pf~rd.".. M. I I I -
12* (frnm MOM. Pure pyffule Itu 110-1*. xj* I,WK
11:00IMM, Purecalltaxotem.,-W. PAM-4ceal lover the
rmal"t Ina If's ott"In XAVe bcd tesults ill the N"ttatim" lit
M (7,41" 1 ul Not'. "hich *etc still bdow the fr4ults will,
AlPi ak"tc. Purr 111. b?m wi.* .4"
11AMM pags.114C of Y) g. I over the Catalyst (W);J,
CrA) at Adrom1min. at I'M* gave 111.5g. condensate an,[
14.11. grm (0.4% OLl. 0~2.%% CO. 11% C0j. 21% olefinq, Wq
Men". 4,107" 11); the liquht carittentale cave fordow. b. '.'?4
al? 1,4M., St. KVW4,41.10

,do of -in
Actl ftlutvfm~a at Glirtfu-beaft
Wo - V k
wun-balwe
Vur' =11.). *h.",:
COOM
OXG t Kinsm, Gen. Chcra.) 21, 973-NX1951); d.
CA. 43. &WA. W-Me.-Comparatbre fmr0eity studies of
Pb%lft anti ali hAdc &min" with fumnWine (1) showed
It
tkAt fit teaciiens of I with inked HtNils and Mils. POW*
'its vul Ph
ItIllf PhNiff, INS -Nih. and MlQhC%v!&Ml"t- and
thtm Is (Qntterl (11) white If*
CrArIkmo with smM44ty Amin" (PhNIM, Ilb!41111-1r,
PhNIIII(f And Cyck4etvUllIff"t), act rommi It, AM.
tuft, and ;rv;;4 of blylayl(M). PvAttg 10g. C lig. PhNIft.
dud ICN'All 4(Jk)"gAVt
(I's C. I-dA)(PrFoAl4xd' b'. 14-10 (Irk-latc, M. t83-64 1.
a 7C.
PhN a. an from 2 tombintd rum). 1 (9 S.)
I NIM d=11ar y cxve&Sl7. PhNifs and Illv' It.
all as (bolated the ditaximide, Wrv) arid IJI
wen
(isolaCed " the fetrubmaLl-W. I (S g.). 4 g. PrNife. an,l
64 C. MOW duly 921V W% Ph*,Ilt arid 10% 11.
MA a* the d0non, , 78%). and a trace of
tit as above), 1, OUNIff. amd Pb%'Ifo fikmise pvc
ArAf. 5phniff 40' a- I with PhNI(Ifu 1IM114fly
gave 67% pnbqlfs 11% it, as well &A (%% C411. and a
littlellf. I with PhNflonrul cVctaftexV1*m(ne(.":I:J mclxr
ratio , 60 rg'CyC(Qhrxtne' M% PhNift. and 4% U:
at 1: 1:1 Mda 47m, 62.3% 4Md M%. Mp.. Were fOCITted.
A 1. 1 MOW MISCOf I With OVkhtsYlAlliti" gmvr 414M v7rf~

Vur W 4tul 1, S. LVvt txfa~~M ScAle, 1711wi V';1L:f;"
Afa. Mcak S-N.S,R. 73, 72Ntql%1P -li(iiClIpAill
(1) 4 142 g;) p4w-l " At^ in :4 %rAk otcAut 4 N, ist
If)#, jhf- lit 00" COVO 121 W. VAI All AMP, 44 14 lifth I hO IVA,--
fk-ts No Of-M" (80 clif than^ txvvt fiol kut ~ 14 iktrm4-
tied by the Karmen stiftfruns ma A'twtf 411 Alf~-(~fO ~1111 Ift-
CM). and IN@ (facli'm N. ILI A 5 V (W 0 ) 64 . jllkt. if
allyl anti Pr 4k-s. FrartficT ditto of the Aq, twt t4 the
VAIdTfAte YkMfd UNC11211011 W 9. 1 AM 3 9. (XClltCJlr
41711,01U.4 At 3501. 143 C. I Cave P5 C. "t4lyrate (62 ig- Afl.
layer artel P cz Nil, The sq part gAve 2 4 it uncli saigrit li'
the 44-31' ftaefloo (J A N.) k A ftial, (4 AticV.1 uttt.
It# 7*(:Ig ., i f% A 91100,
at 40% PwOlf AM (111% allyl Ak- The fraction b. MI.
il R(elit-ofecito. The Amt.. of ct.1 from 2.5 C. I were
,.Vl and ZIM cc- (S.T.P.) at '-'A) 2nd Xrdi*, And their
CC),. CO.L lit. C.Ifft, 1. C.1j.) At 12 L 4. 2.2.
I$"'. JOL7. (50-0, And at Mill, 7.9). "A' ::'0. 3'M. -'SLp Til-
M4,1141J.-ft" "Xidt, WA. n FD-773
CsC bond In the coilpaund in greatCr than that of the isolated bond.
Orto table.. Pirtc--t-, n7frir,~-ncea (one foreign).
Institution : Chair of Physical Chemistry and Chair of Organic Chemlotry
Submitted : July 10, 1953

2w
:n !"V*trly
f" wt~~ wd
SWA
'4 -1
ii it't 10
2W. 'j
t ~3v' zou 41.. 1
V~ A(3 I
114(3 . #' il
IJ, rj 2'-,,- .
4r,"" 71
>'z4 ;o
3~
'j" i"j I Ij
j~t r

X20
emis ry Xyeu 'ur-f YD -1 GG 6
Card 1/1 Pub~ 129-9/2q
Author- Yurlyev,-"Iu. K.-and Avbatskiy, A., V.-
Title Dyestuffs containing the pyrrolidine ring
Periodical Vest. Mosk. un., Ser. fizikomat. i yest. nauk, 9, No 8, 63-69, Dec 1954
Abstract Prepared azo dyes containing the pyrrolidine ring by treating N-phenyl-
pyrrolidine with diazonilm salts. JUso prepared tri-Pheny1neethane dyes
containing the pyrrolidine ring by treating N-phenylpyrrolidine with
benzaldehyde and with 1,1ichler's ketones. An indamine dye containing
the pyrrolidine ring was obtained through the oxidative condensation of
N-phenylpyrrolidine with N-kipara-aminophenyl)- pyrrolidine. The ab-
sorption spectra of pyrrolidine orange and N, 111(bis)-tetrejaethylenein-
damine salts are further in the long wave region than those of methyl
orange and the corresponding Bindshedler's-salts. Five refforences.
(all USSR). Equations; graphs.
institution--
Chair of-Organic.Chemistry
Submitted June 19, 1951'

)~tJ R yc,,/ 1A I k-
I . ?, 1~ -
Title ' Synthessin, arl re a ct-;or~3 D" 1 *-P~-.qnpq nf' t I-, t- -k - ~ -- , -

ci -,vnrcuj ~p - p- -- -- - - -- - - . . A -!,, -A 1~ 1 T ". 0 ~ 0 . : . 4. - , ; . . ". -

~ v - I I . ;P.
- . "! -, I f , -

:: r

Title f U-~ in i ~-- ~ ~v Lni'-, - :-,nn nr-t:i-arv~ -,'-:ri u if; ~iz~ i

Author& 16
ry,3 v an,-,
)
Title
_x the :)rpsence of slu-
E ca L~,
Periodics,l 71,mr. ob. kh i-r. 24/8, 11,444 1LO, Auglist, 1954

Abstra:t 7-11, Orl~; ,Cts obtained 'rom iclvrlratinn of --.-r-

at I Z;ns -r --I- t h i t ~.p -I T-T,
instit,ation : State University, '-Ioscow
Slibmttcd : Ihrch 1~, 1954

mpm/ Chv--Pi5try
ane thr ~ut
T 1 t, 1- -1 - r1 - j nyl t h h,
Abstr,tct 7ie gffect rf furthpr alk-i-I en-mlication In the basic 1~ta-alkyLPiranid-
~e-,-arb-n Atr)-. ~f '~hP fllrq-li iinR c7cle, -Tlev-3n USCR;
'ubml tt-i ,~ch 22,

41
Ty
C A.

L
It

Pin

ob.

~ - - i

C I t k'i

9."~: tip

~'%A A
4it,

NOVOSMVA, A.V., otv.rede, TOLIVIOTICH, S~Iaq red*; GBRASIMOT' Ya.l.'
red.; YURI YET, ru.K.., r ed.; MI YZVA* L*P* . red*
[Department of Chemistry of Moscow state University] Khimi-
chaskii falmlltat Mookovskogo ordena Lenina i ordena Trudovogo
lErasnogo Znameui gosudarstvannogo universiteta imeni K.VwLomonoso-
va. Moskva. 1955. 59 PO (KIRA 13:6)
1. Moscow. Universitet.
(Moscow University) (Moscow-Chemistry-Study and teachiag)

y
ZELINSKiT. Hikolay Dudtrlysvich, 1861-1953 (deceased] WARSKIf. B.A.,
akademik; BALKOIN, A.A., akademilz; WCHISMV, X.A.; SMU119, V.I.;
KAVMNNA, Te.D, doktor kbinicheskikh nauk; LXVIYA. R.Ta.. doktor
khimichaskikh muk; FIAT3. A.F.. dektor khtnicheakikh nauk;
03IMMIM, A.M., daktor "imicheakiMi nauk; YURIV-xv. TUA.. doktor
khimichaskikh nank; KISXUVA. A.A., telchulches?w 4.
(Collected vorks] Sobrante trudov, Moskva, Izd-vo Akadenii na'uk SSM
Vol. 2. 1955. 743 P. (WaA 8:n)
1. Chlen-korrespondaut AN SSSR('for Koeheshkov and Shmykln)
(Hydrocarbo=) (Patrol, ~, - )

21

ILI,
a T ht RA
73NIT
'X '! i -" ~o4i.
!o-v. UN ,
'%~ 1 0.- , -') t38--

i
, I
- 4

YURIYZV.YU-K-
a& mpoxmds In the
The chamistrY of jaydrocarbons and h teracyclic co
works of.H.D.-Zalinekii and his school. V66t# Kosk. un, 10
no.45:145-167 Ap-my 155. (Km 8:8)
(ay0ocombons) (Zeliaskii, 111kolai Dmitrievich, 1861-1953)

KOROBITSTItko I-K*; YUR IYEV, yue K*; LUXIVA, Yeetis
id fro2s -furwidone.
aminofuranidine ard dIglYcOlic ac (KM 8-7)
ZL-,ob,khim, 25 no .3.1,563-565 Mr '55-
1. )40akovakiy Gosudar3tvGW universitet*
(-ruran) (DiglycoliO acid)

t~h C"eT

f to imam V-W~L
7 SL4cnN-
. -

h HIS '11~
wwv Nui,
-'1 C7
rt-
Vql'

AID P - 3582
SubJect USSR/Chemistry
Card. .1/1 Pub. 152 - 19/20
Authors 'ev Yu. K!, A. V. Arbatskiy, I. K. Korobitsyna.,
and ev
Title Preparation of N-phenylpyrrolidine from 1.4-butaned.Lol
and aniline in the presence of aluminosilicate
Periodical Zhur. prikl. kh1m., ?8, 7, 781-7820 1955
Abstract Under optimum reaction conditions the yield of
N-phenypyrrolidine obtained was 66.1%. The-prepara-
tion is described in detail. One table, 5 references,
all Russian (1937-1950).
Institution None
SubmLtted Je 30, 1954

IjV

45

I L
7 1- r

YURI Y&V# -yu-41E., prof 0; - tNSttNYAuOv, A.H. - ak-adeImik,- o-tv.red.
Ileboratory work in Organic chemistr7; program for -the ChesistrY
Faculty] PrQgrammii praktikums po organichaskoi khimil (dlia
khtmicheskogo f6kmllteta). 1956. 14 p. (H24 11:3)
1. Moscow. Uhiversitet.
Whemistr7, Organic-Study and teaching)

/ 1_4 r ' e ~_ -/ / 114 , /~:'- ,
USSWPhysecal Chemistry - Moleade, Chemical BorA.- B-4
Abs Jour: Referat. Zhurnal RhImIYa) No 2, 1958o 3575-
kathor : P.A. Akishin, N*G. Rambidil Yu. X. Yurlyev.
List :Macow University.
Title :FaMan Spectra of Heterocyalle Compounds, 171.
Orig Pub: Vestn- mosk. un-ta, 1956,, 061-67.
Abstract: raman spectra of ten sulphur containing heterocyclic ccmpouads
trimethylenesulfide, thicphene,. 2- and 3-methYltetrahYdrothio-
phenes., '2.42-.9 3.93', 2,5-, 3.,4- and 2,4-dimethyltetrahydrothio-
phenes and tetrahydrothippyrine vere obtained. 'Vae line inten-
sities were measured photom6trically using one and the same ob-
jective scale. The cbmateristic of the differential band in-
tensity of the C-3 link valence vibrationn JS-j3hown. An except-
ion Is the intensity of the frequencies 0 (C-3) in th-- 3,3-dimethYl-
tatrMhY(IrOih:LOPhene spectrum, which surpasses the others by 20%.
This fact is explained by a possible interaction of k~ (C-S) fre-
Card 1/2 -43-

USSR/Physical- Me-mistry --tfoleaule,,- Che.mical- Bond. B
Abs Jour: 10ferat. Zhurnal Khimlyap No 2,- 1958P 3575.
quencies with holosy=%etrical vibrations of the group containing
the qvAternary C at=. The Intensity decrease of (C-S)~ bands
in compounds baving conjugate C-S azd C=C lin , for example)
in 4--l-dihydrothiopyren and thiophene, is noted. See part II
in RMMim, 1956, 53677.
Card 2/2 -44-

Ly
YuEtlyLlVv YU.Ko; aEMM, L.S.
heats f
0 14 //3 -mere apt oethyl) -ar7lamines and ir-( /If-mereaptoetYql)-
pyrrolidine. Yest.Mook.un. Ser.mFtt.,makh.,astron.,fiz.,khim. 11
no.1:197-199 156. (KIRA 10:12)
1. Kafedra organicheakoy khimii Moskovskogo universiteta.
(Amines) (PYrrolidine)

YUR'YEV, Tu.K.; YSLYAKOT, G.B. ; IMLYAKOTA, Z.V.
Cyanoethylation of isolpropyl-2-thienyl -ketone. Vest.Kosk.un.
Ber.mat.,mekh.,astron.,fiz.,khim.11 n0-1:201-203 156. (miRA io:12)
1. rafedra organicheskoy khimii Hoskovskogo universitsta.
(Thienyl ketone) (Ethylation)

V'L' /V- jy'~~ I/VA-
LIVINA, Royal; YURIM, YU.K.
Acadendolan 4&. fa-~tkinls studies in the field of chemistry of
alio-yalle hydrocarbons and.their derivatives: on the-occasion of
the 80tfi anniversary of his birth, rest. Mosk, un. Ser. mat. makh.,
astron., fin,, khIm. 11 no.Z:121-13Y 156. (14IRA 10-.12)
1. Ufadra organicheskoy khimit Hookovskago gosudarstvanuogo univer-
siteta.
(Nametkin, ffergel Samenovich, 1876-)
(Alicyclic compounke)

MY:

7..: A- t!lv

' v:CMI af
7 L~:.~
py rr

'Mm

:vlt vp I~elvfly e e
A A
g5lz

dj
,
-4!
.z

71' i
-Ft
r yi'i`;~

kii, I Ii .
I : : I., ~ ~ ., i -
.. i , i * I
. --l--.---.-.. -- - .
,"!.-

., P ; ,
I . t:. . I
~ f.-; :
. f ..., I.-
t, f lr~.
r i

ft'YBY, Y V.I.; GMRW, L.S.
Aruthests of 3-aa7l- and 2,3-diarylthiatolidines. Zhur.ob.khln.
26 no.2;350-353 F 156. WRA 9:8)
l..Xookovskiy gosudaretvannyy universitet.
(Thiazolidins)

TEIRIYET, Yu.K.-, LUXIMA, Te.M.; FOLdn"Ov. YU.M.: TOIAKOV, Y.F.
Catalytic conversions of heterocyclic compounds. Part 48. Prepa-
ra;ion of 3-isoamyl- , 3-hexyl- , and 3- P-to'Lyltatrabydrothio-
phones from corresponding furaniaines. Zhur.ob.khim. 26 no.2:
553-557 Ir '56. (HLFA 9:8)
1. 14oakovskiy gosudaretven"y universitet.
(Thiophone) Oruran)

AY
uf x
llrcii Diu'
;Orr,

~ TOR' Y9V -Yu.K..- YILYAM, G.B.; VYSOKOSOV, A.M. -
-
Tetraacyloxysilanes in the synthesis of r_,j.3-uneaturated acids.
Part 1. Synthesis of cinnamic acid. Zhur.ob.khla. 26 no.3:926-930
Hr 156. (Km 9:8)
1. HoskovskLy gosudarstvannyy universitat.
(Cl-nAmic acid)

Mem, Yu.K.; SAMAU. U.K.
Chemistry of selanopheas. par-, 2. Acylatioa of 3.4-dimetiqlgeleo-
v
phene by tetraacylozysilanas. Zhur.ob.Wm. 26 no-3:930-933 Kr 156.
(KM 9:8)
1. Moskovakty gosudarstvennyy universitat.
(Selenophene) (Silane) (Acylatioa)

8A

USSR/ Organic Chemistry - Synthetic organic chemistry E-2
Abs Jour Referat Zhur -,Khimiya, No 4o 1957) 11649
Author Kor obitsyna I.K., Yurlyev Yu.K. Shvedova S.N.
Title Synthesis of l,4-D_M1_n_oB_uRanone-2.
Orig Pub Zh. obshch. khimii, 1956, 26, No 6, 166o-1662
Abstract 51 9 of 1, 4-dichlorobutyne-2 are 'stirred for 8 hours with 2 liters
of concentrated NH OH, acidified with concentrated HC1, evaporated
70 hours, extracM with other; yield of 1,4-diaminobutyne-2 M
37%, BF 82-840/ /6 =, MP 41-43'. 5.4 g I in 360 ml 10 solution
KOH are shaken for 3 hours with 18.4 gC61f Coe' to convert to N,N'
-dibenzoyl-1, 4-diaminobutyne-2 (3:1), yiela 90.3%,'14P 2100 (from
alcohol); 15 g 11; 900 ml 90% CH3CWE and 6 g M04 allowed to
stand for 12 hours, heated 20 hours at 70-800, filtered, solvent eva-
porated, added 300 ml water; yield of N,N'-dibenzoyl-1, 4-diaminobu-
tanone-2 (111) 72%; 3 g III boiled 30 hours with 75 ml 98% CH COOH +
75 ml concentrated HC1 (added four times 10 ml of Eel). Sol2ion
decolorized with charcoal, evaporated in vacuum, and extracted with
ether. To almost dry residue added 35'ml alcohol; at 00 the hydro-
chloride of 114-diaminbbutanone-2 separates out, yield 65%, hT
215-2160 (decomposition).
Card 1/1

w; N I I.,

V-, N;

1.J 4