SCIENTIFIC ABSTRACT FR:MAJOR, R. TO:MAJOR, A.
Document Type:
Collection:
Document Number (FOIA) /ESDN (CREST):
CIA-RDP86-00513R001031400021-6
Release Decision:
RIF
Original Classification:
U
Document Page Count:
99
Document Creation Date:
November 2, 2016
Sequence Number:
21
Case Number:
Publication Date:
December 31, 1967
Content Type:
SCIENTIFIC ABSTR
File:
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APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
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APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
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APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
~'~~ ,~; .
R~.~rt1:VI~/fiwne,n and !~:ni;aial Ph
y..iolo~,y -Metabolism. V-~
r:bs Jour Ref 2hur - Bial., No ~, 195, 17977
~uthc~r B. i~,jo~:', P. Doczy, G. ~Co~.~r~a, S. t~~gyuri rind :~!. Jazzfp
� -
Inst ~-~ ,.._,...,~.,..
T~.t1e nai.ly Ctzs.nges in Bloc:d Iron Content.
C!rig Pub Coriun. acad. R~:~, 1U57, 7, No 2, ~ 67_271
'abstract eleven rlums~n subjects *r.'ent w1.tY~c>ut f'~~c~cl curing the dt:,y ~.~zd
toc~lc their men ~.s 1't nit Frith the ordinnry l.ntervrzir bet,_
~~~een them, during, ~.'hich they c= '_P_qt. It bras f'~~und. that the
~.ron cor.;tent oi' the blac~d decreased gr~,du~�~,i,ly end reached
its lo.�est va,~.ue at abnut noon of the following dFy, dust
~:s axons; ;,ersans eating at norm, hours the ~~uim~^! reduc-
tior. in blood iron content occuxz�ed towazd midnight.
t,along the indivic3u;~ls taho received nu fraud. r.~1.zz'in~ the ~.=:y,
the iron content of the bioad increased torrarci evening,.
2'he dr~il;y ch~nge~; in blood iron content, as the r,~uthrrs nc1-
te, are ,~.ssociated ;ritt~ food intake.
Card .~~ 1
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
APPROVED FOR RELEASE. 06/23/11 CIA-RDP86-0051 3 8001 031 400021-6
~+ ~7~~~.
l AtT~pR,� ~trhae~ Los~at-t tDaator~tBudapestl Ms or A
Horba,la (13ucht et) ; ~ ~:~..:~:x:~:~~,, ~ ,,, Cpeat, t Vermes,
~~
TIZ7,~s Stud~ea on i~he glucoeidee of ac;acetiae. Part 1S gynthsei~r of tilf~ine
a flavonegl~toosi,de of 'Ti1,ia, Japonica ~#.monlca3, +
I SOURCES Academia ecientiarum huagaricae. Acts chimica, v. 42, no. 4, 19G4
' 395 ~ 393-
.. T+OPTC TAii~s ~c'bo~Yldrate, argaa3,c synthetic process , -
Abstracts ~Genman� article] The g~,ucoside occurring iA Tilia ~aponice
~S~mcnkAi, tit;tatcine, -Was sgntbeeised with the aim of establishi
- � _ ~ structure. ~~s s a8 its
� "acacetit~~ ., ;. iYntb+rsis aas accampli,Sh~;d thxough .the pxepmratioa cf
~' ~ D ~lu~sreide.p~antaaceCe~e Qtiitanit~e Aentaaa+~tat�j, ~e ~,
pr+aduct wait tilent~ti~~d bq ~attf of r1Se synthesis ao i
a~txavio-let e~rectra- with those � of the natural n~~erialh as~ari~ its ,
~,a`diby~lr�~~-�etb` flavone-~~ �U., lucoride rith a melti
�f 2S9-a62�C. ,~ n a amore " ~ ----~_ _ _ ,.. ._ __ -. ~8 point;,
eacpreen they ~~~o the ~~~,,~,;~ ~,~
Sai+,n~~+e far ta~,a
8~~t of this agrk ~d t~,t Ip ,S'"'a-~~ !or hem of
aco~~~plien~'. 4t the , mlaro eumais. n .g~. e~�t, hear ~ formals. .
i ~r~. 7 /9 . , ,,,
- __. _.
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F;UNGARy/C7rgc~nic C~e~mi.stry - Pdaturally Occuring Subs tances G-3
and 'heir Synthetic Analogs.
Abs Jour ~ Ref 2'11ur - Khimiya, Plo 8, 1958, 2525
24 Hours, dissolved in 0.3 rRl absolute alcohol, and ~n
eoolJ:n~ were obtained the d~~,rk red crysta,.l.a of D-~.l,uco-
zone��formazan / (I`1,~t' -cliphenylforr.~zyl)-D-arabotetrahy-
droa~~-butyl ketonel (TIT) IZP 163`, yield 0.22 g. 0.15
g II ~C were dissolved in mi.;rture of 6 r:S ~laeial CHI CGOIi
and :L.S ml alcohol, with moderate heating, and 0.05 g
phen;}rlliydrazine were added. After standing for ~+.5
hours, separation took place of violet crystals of I
(0.03 g). The mother-liquor was poured in I~0 ml water
~ and 'the precipitate of I that separated was filtered ofi'
(yie:Ld 0.04 g). On combining these two products crystals
were obtained fror.~ a solution consisting of 6 parts pyri-
dine and 15 parts ethanol. The identical. nature of cara-
poun~ls prepared by these two rriethods proves not only ~thc:
structure of I, but also the fact tYict in the molecule of
II t;he phenylhydrazine residue is adclecl to C(1), sir~cc
Card 2/3
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. .~.~~ I1~fI ~i ~ r_, tk=: , ~~ ~ ; ~ ~,
' 1
Occuring Substances G"'
HUT1C�,'~'l/Or~:nie Chcanistry - rdatura.].ly
and Their Synthetic E~-na:Logs.
Abs Jour Ref ~~hur - Khirniyrz~ P1o ~~ 195~~ 2~26a
Author P4ester Las zlo ~ p~,~or Acs M
Inst : - ~~ pose of
Title Synthesis of D-Glucosazone I'orr~a.2on for the Purf
P~.^oving Tts Structure.
u,r tud. akad. Kerr. tud. O52t. kosl. ~ ~-957~ ~~ rto ?-3,
Orig Pub Maly
38~-�383
To ~~rove the struc~tuz'e of D-~1.ucosazoneform~.zan (I) ~
Abstract -, ucosaxone and C H,T1.C1 in alkaline al-
obtE~,incd from D gl. (, ~ ,r-
cohl~l solutions synthesis of T was effected by another
method. 1.62 C D-~.ucosone-l.-phcnylllydrazonc (IZ) were
idine and at -5 � was added a s~-
dissolved in 16.2 g PYr' 6~ aniline After standing
lution of C_HSN~Cl (r'rom Oe g
diluted 5-fold with ice
~3p i:>inutes~ the solution wAs
water, the resulting gurIl~Y product was filtered off After
Card 1~3
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