SCIENTIFIC ABSTRACT FARKAS, L - FARKAS, M.

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• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

CA T,7)3,)P Y
ABS. JOUR. rtZKhimo) Ilos 1
A U 'A V OR
C.qjC-
pUB. :
icontld
1960) Yo. 1201~
: aro indleatorl): Ia, 18; b, 19; C, 35; d, 35;
a, 39; f, 56.-- L. Vinograd
3/3

Country Hutleary G-3
Or-togory Orgia-tic Chemistry. Nntural Ocx4pounds and their
Synthetio Amalooes.
Abs. J_-.ur-o:Ref. Zhur.~Ehimiya go. 6, 1959 19623
:Zemplen, G.i Farkas L ; Rakusat R.
Author
inr,titut. :Hungarian Acal"h~eOY-0 lKiencas
Titlo :Structure and New Synthesis of Scutellarein.
Orl,S*Pub. :Acta chim. Acad. scient. hung., 1958, 16,
No 1+, 445-449
~AbBtract Bromination of 1,1+5 g of 6 1+1-diacetoxy-5,7-
dimethoxy-flavanone In CHC13 under irraEation with ultra-
iviolat light gives its 3-bromo-derivativeg yie1d 0.4 g,
MP 164-1650 ?from alcohol); 005 g of the latter heated for
5 minutes with 1.5 ml 30J6 solution NOR + 15 ml h1cohol and
isolated 0,25 g 6 1+0-dihydroxy-5.7-dinothoxy-flavone (Ii HP
2631, (from alcohol). Diacetate of I, MP 2000 (fror, loii'olii.
Saponification of I by boiling with HBr in glacial CII-tCOOH
(2 hours) and subsequent acetylation give 5,617941-te~racet-
oxy-flavone (IVI MP 238* (from GH30H), which on heating (for
3 winutes) with % solution of NaOH + alcohol, is converted
to 59697941-tetrahydroxyflavone - scutellarein (11), aglycone
11 n 1"0'
tj~' : 112

C~)iixitry Hungary
CCt C;-fj:) I. j --
Abz;, Jour,
Aut'- or
Titlc
.OrIG. Pub.
G-3
19623
Abstract of one of the glucoside of �cutellaria altisslaa
L., which does not melt up to 3000 (from CH30H). I and II
obtained in the same manner starting from natural pecto-
linaringenine (compare RZhKhim, 1959, 1456). V. Bykhovskiy.
Card: 2/2
ILI

MWXY/Or3anic Chc--iistry. GrUnnic Synthesis - G
Abs Jour: Ruf Zhur-Khim., No 11, 1959, 38631.
;.uthor Farkas, L.
List
Title The *.cylntion of ;,etive Methyleno Groups. I. A 11cw
Synthesis of IsofIzvone.
Or.'L: ikib: MaLVar Ken Folyoirat, 64, No 4, 136-318 (1958) (in Iun,-arian
with a Genman s=nry)-
,%botract: It has been found that the action of ;lry IICI on an
ether solution of substituted 2-hydroxyphonylbenzyl,
ketones (i) in the presence of Zn(CN),;Z,, leads to
the formtion of beta-ketoaldiuines, which oa hydro-
lysis are converted to a tautoneric aixture of beta-
hetoaldchydes and alphahydroxynethylene ketones.
Card 1/3

.1
MAIG:M/Orcaniiic Chenistry. OrL=iic Synthesis. G
;,bs jour: Bef Zhur-Ehim.p No 11, 1959, 38631.
The latter on rin(; closure (with hydroxyl [;rctrp
in the 2-position C;iva the correspondinC; isoflavones
(II). Dry HCl is Imssed through 50 r.11 of an ether
solution containint; 3 cps 4-uethoxy-I Culd 3 Gns
Zn(CN)k (cooling is aIrplied -t first; In the later
stages the teuvrature is raised to 200); 1.2 Cp of
7-mthoxy-II (Ila) are obtained, rv 158-1590 (from
ale). Dy.tho application of a similar procedure,
11.8 am of 7-hYdroxY-II (ID)p pp 2140 (from C11joil)
are obtained fror, 5 gis 2p4-d1hydroxypLhcny1bci1zY1
ketone and 5 Cps Zn(CIOA,- 0.5 Cp Ilb on acctylation
with (CII;CO),XO in the rjresence of C11 COOITa Ldves
'-o
7-acetoxy-II) up 136 . When 0.4 gi qIb in 12 ml acetone
is refluxed for 5 hrs with 4 ml CIIJ in the presence of
2 Gos Kk~Oj, 0.5 an of IIa is obtalned. 5 cus 2,4,41-
Card :2/3 G-34
Card :3/3

COUNTRY
'
tr
tural Gqmpound-n and
CATEGORY a
a n lorues.
ir Svntlnetilc~rTrz

TOUP
.
-

joTj?
1'e
0~ 2 C,
f7,
Od

2M 0 PY,
CA
A F: J OUR, 5:')

C.,: ll~- Fu 6

V.
Bal)t,51,9 t ~gr
investigation of the 11yeosides of
of pseudobapti-enin. P.217
ACTA CHIMICA. Budapest, Hungary. Vol. 19. no. 2/39 199
Simplified -.7ntheses
Rnnthly List of East European Accessions OW), LC. VOL 8, No. 9. 5eptember 1959
Uncl.

FAIMU, L. ; 3 CHUID,R, X ZEM`il, 0.
A new synthesis ct genistein. p.277
ACTA CHIMICA. Budapest, Hungar7. Vol. 19, no. 2/3, 1959
Monthly List of East European Accessions (MU), LC. Vol. 8, No. 9, September 1959
Uncl.

FARKAS, L.; VARADY, J.
Polyoxy-chromones. I. Structure of 5,8-dimethoxy-7-oxy-isorlavone and its
derivatives.
ACTA CHIMICA. (Magyar Tudomanyos Akademia) Budapest, Hungary. Vol. 20
No. 2. 1959
Monthly Lists of East European Accessions, (EEAI) LC, Vol. 9, No. 1, 1960
Unal

FARKAS9 L,..,- SZANTHOj V.
Investigation of glycosides of Baptisia tinctoris. Lo Ie A now synthesis of pasudo-
baptiganino p*93.
MA(ffAR KENIAI FOLYOIRAT. Budapestj Hungary. Vol. 65, no. 3P Mare 1959
Monthly List of Fmt European Accessions (&AI),, LC. Vol, 8, No. 9, September 1959
Uncl.

FARM, Larap4j- VARADY, Jozsef
Flavonoids of Soja hiopidao Pt, 1, Magy kem folyoir 65 no,3;94-
96 Mr '59o
1. Budapesti Muszaki Egyetem Szerves Kemiai Tanazake.

FARKASj, L.
Acylation of active methylene groups. 3:1. A now synthesis of poeudobaptiganin,
formononstin armi other inotlavormo * p*105
MAGYAR KEMIAI FOLYOIRAT* Budapeatj Hungary* Vol. 65., no- 3., Mar. 1959
Monthly List of East European Accessions (EUI), LC. Vol. 8, No. 9, September 1959
Uncl.

COMMY G-2
CA7WMY
1ABS. JC'tM-I RZKbixop No. 5 19Wf NO*
kunic-R t Farkas, L. and Varady, J.
1IMST. N ~ ~- -0v e ni-
T1 T11 -.11 The Structure of 5, 8-DimethoXY-7-flydroxyisoflavon
nnd Its Derivatives. 1.
ITC,, 11M, t Magyar Kem Folyotrat, 65, ;j0 5, 186-188 (1959)
~~TJUGT t ~1,8-limethoxy-7-hydroxyisoflavone (1) has been
synthesized from 2,4-dihydroxy-3,6-dimethoxyphenyl
benzyl ketone and HCOOCF5 by ring closure. Metby
lation of I did not give the product synthesized
earlier (A. Ballio and F. Pocchiari, Gazz Chim
ital, 79, 922 (1949); 11. Naranimhachari et al,
Plroc Indian Acad Sci A, 359 50 (1952)) to which*
the structure I has been aBsigned. It has been.
established that the product described earlier
(see reference abqve) is actually 2-hydroxy-5,7,8
'CAPPI 1/3 163

Hungary
CATEOCIRT i
ABS. JOUR. t RMbel NN 5 1960s Not 17838
MIG. PUBS
-trimetlioxy-2,5-dihydroinoflavo,-ie, which wider
the action of OHICO).O in pyridine is quantita-
tively converted to 5,7,8-trimethoxyisoflavone.
The lart product does not given tne Bec-ker rear-
r.'31;xement with ii.9r. The derivative and ti,.c ir.
are given: 2,4 -dihydro xy- 5,6 -dime thoxyPj2un,,.,Iben zyl
ketone, 103 (Oxime MP 173-1740); 7-hydroxv-';,8-
t dime thoxyinof lavonit , 25).-252; 5, 8-di-mothoxy-7-
acetoXyisoflavone, 145; 5,7,8-trimethoxyisoflavone,
167; 2-hydroxy-3,4 . 6-t rime t hoxyph en.~, I benzy! ketone,
PD

r ttit;-
,r,
rt
G- ?
I Hungary
iou -
JMR. i RZYhim., No. 5 lgwt No# 3 8
1 AU?XCR s
I -.iZ T.
A~

V, 941
flavine, 156; 5,?,8-trihydroxyi&oflsvone,
5,7,8-triacetoxyisoflavore, 5-hydroxy-,),
8-dimethoxyicoflavone, 158-1591 7,8-,AmethoXY-5-
acetoxyinof-linvon(" 103.
Fyurst
CAIM s 3/3 L064

Hunsary
(;A7!*.-';-'-C.R Y I
j ln~" ARM. t RZXhtz9,F Noe 5 IW' No, :L&'026
I Zemplen, G., Farkas, L., and Schuller, N.
1 140~. given
T TI F"
1l v Soja hispida Playonoids. 11. A New Synthesir. of
i Geni5tein
CRIG. FL M.. s Magyar Kam Folyoirat, 65, No 5, 169-192 (1959)
A t3rMACT I The authors report the synthecia of genistein
(5,7,1~'-trihYaroxyinof'Lztvone) (1), the aglycone
of the glucoside of S. Hispida L. Starting from
tt',e dimethjI ester of fluoroglycine and p-r-ethoxy-
benzy1cyanide, the authora have prepared 2-hydro7y.
4,6-dimethoxyphenyl-(41--nethoxybenzyl)-ketane,
which on ring closure gives 5,?t4'-trImethoxyi6o-
flavone (II). Under the act-lon of HBr in gla-dial
CH3COCH, II is converted to I, mp 296*. Other
substance3 were synthesized by a simila-r procedurri
1/3 197
ITI

i lit- Al'j,
C4 Ml; CRY I
18o26
JABS, JMR. I ARMAmps Not 5 IWj No&
A r--S',V A r,,Tt(the sut)stance and mp iv *c are civ4un) ;.-I-meth3ri-
5,7-dimethox~ristflavono, 1391 2-methyl-5,7-dihy-
drox.visoflavone, 228: 5,"-dimothoxyisoflavone, i
215
ll;~-; 50-illacetoxyi.130flavone, 17?:
isoflavone, 205:
39; 2,6-dimethc,xv--,,-
';,,fdroxyphezyl-(41-me'hoxybenzyll-ketone, 73; 2,6-
~imothoxy-4-Raotop'he'noxy-(4,-Me'choxybenzyl)-icetome
1371 e,6-dimettioxy-4-hydroxyphenyL-(41-mot~ioxy-
benzyl)-kotone, 73; 2-r~ethyl-5,7,41-tritnel,,Ioxy,.So-

-J3'
W:
I-Di
3/5
r y
Rmim'.. NO, 519660j, 110.
navone, 1FI; 5,7,40-trimethoxyisaflavone, 160: 5,
L 41-triacetylflen~s-
7,41-trincotoryi5oflayon- (5,7
tein), 202, 5,,,,4f-tri*enzylhydroxyi_~of'.avo.-~e 244,1
1960, No C." ;195-
For Commiliticaticn I #3qe RZhKhim, V. Fyurgt
198

FARKAS, Lorand; PALLOS, Laszlo
Final structure and synthesis of coreopsin. Magy kem
folyoir 65 no. ?.-278-280 J1 159.
1. Budapesti Muszaki Egyetem Szerves-Kemiai Tanszeke.

FARKAS, Lorand; VARADY, Jozeef
Flavonoids of Soja hispida L. Magy kem folyoir 65 no. 9:
371-372 S 159.
1, Budapeati Munzaki Egyetem Szervea-Kemiai Tanezeke.

FARKAS, L. (Budapest); PALLOS, L. (Budapest)
Natural polyhydrmW-bensalcounaranmes (aurones) and their glucosides.
Periodica polytechn chem 4 no.1:73-76 160. (EM 9:12)
1. Organisch-Chenisebes Institut der Technischen Universitat,
Budapest.
(Glycosides) (Aurmes)
(Benzylidenehydro7b~nzofuranone)

ZJWLEN, Geza (died in about 1959); FAMWILorand (Budapest); SATTLER, Tamas
(Budapest)
Polyoxychromones. II. Synthesis of 2g6-dinothYl-7-hydrmW-isof3.ayme
and 6-xetbyl-7-hydrmW-1st)navone. Acta chimica Hung 22 no.4:449-4%
,6o. (Ew 10:2)
1. Institute of Organic Chemistry, Technical University, Budapest.
(HydrmWchrmw.e) (Hydroxyisoflavone)
(Hydroxy tbylisoflavone) (YAtbyl group)

F~~AS, Lorand (Budapest XI, Geller ter 4); VARADY, Jozsef (Budapest XI,
Oblle-F-ter 4)
Data on the ring isomerization of isaflavones. 1. Synthesis of 5t?,
8,41-tetrahydroxyisoflavone and 7,49-dimethyltectorigenin. Acta
chimica Hung 24 no.2:225-230 160. (EEAI 10:4)
1. Institute of Organic Chemistry, Technical University, Budapest.
(Tetrahydroxylsoflavone) (Isoflavone) (Methyl group)
(Melting points) (Tectorigenin) (Iodides)
(Fiperidine)

FARKAS,, Lorand; PALLOSp Laszlo,- FAAL, Zoltan
Final synthesis and composition of sulfurein. Yagy kem folyoir 66
,4.no- 4:121-123 Ap'60.
1. Budapesti Muszaki Fgyetem Szerves-Kemiai Tanezeke.

ZEMPLEN, Geaa [deceased], PARKAS, Lorand; SATTLER, Tamas
053mthesis of 2,6-direthyl-7- soflavone and
Polyoxy chromones.II.L oxyi
6-methl-7-oxyisoflavone. Magy kem folyoir 66 no.9:335-338 S 160.
1. Budapeati Mussaki Egyetem Szerves Kemiai Tanazeke.
f

PARKAS Lorand- PALLOS, Laszlo
Synthesis of palasitrin, a glucoside of Butea frondosa.
Magy kem folycir 66 no.10:391-392 0 160.
1. Budapesti Muszald Egyatem Szerves Kemiai Tanszeke.

.FARKAS, Lorand; VARADI, Tozoef
Ring isomerization of isoflavones. I, Synthesis of
5.,7,,8,,/+- tatraoxyisoflavone and dimethyltoctorigenin.
Magy kem folyoir 66 no.10:413-415 0 160.
1. Budapeati Muszaki Egyetm Szerves Komiai Tanszeke.

FAPJW , Lorand; VARADY, Tozaef
Ring isomerization of isof2avones. II. A new synthesis of
tectorigenin. Nagy kem folyoir 66 no.n:446-447 ir l6o.
1. Budaposti Muszaki Egyatem Szerves Komiai Tanazeke.

FARKAS, Lorand; PALLOS, l,asalo;-HIDASI, Gyorgy
Synthesis of cernuosid and aurousidin. Magy kem folyoir 67 no.9;
388-390 S 161.
I.Budapesti Muszaki Fgyetem Sserves Kemiai Tanazeke.

FARKAS, Lorand; VARADY, Jozaef
Polyoxychromones.iir.new synthesis of isoirigenins. Magy kem
folvoir 67 no.9;390-392 S 161.
1. Budapeati Muszaki Egyetam Szerves Kemiai Tanazeke.

FARKAS, Lorand; VARADY, Jozaef
.rdng isomerization of isoflavoned,III. Synthesis of 3'-methYl-
isoirigenin and 7,31-dimethyl-irigenin. Magy kem folyoir~67
no.10:431-433 0 161.
1. Budapeati. Muezaki Raetem Szerves Kemial. Tanazeke.
-1

PARKAS, Lorand; VARADY, J*ozaef
Ring isomerization of isoflavones. IV. Direct eynthesis of irigenin.
Magy kem folyoir 67 no.n.-495-496 N I&L.
1. Budapeati Mussaki Egyetem Szerves-Komiai Tanazeke.

FAHW , Lorand, dr. (Budapast XI.j Gellert ter 4); VARADY, Jozsef
TBdaa-peat XI., Geller ter 1.)
Polycr,cychromones. III. A new synthesia of isoirigenins.
Acta chimica flung 32 no.1:101-107 162.
1. Institut fur Organische Cbemie der Techniscben Universitat,,
Budapeat.

J_ARKAS-,Lorand, dr. (Budapest XI., Gellert ter 4)j VARADY, Jozsef
(Budapest XI... Gellert ter 4)
On the rizur isomerizationa of isoflavones. III. Synthesis
Of 7-4wtWl-iaoirigenine and 7,,-f-dimethylirigenine. Act&
allmica Hung 32 no.1:109-213 162.
1. Inatitut fur Organische Chemio der Technischen Universitatp
Budapest,

FARKAS, Lorand; VA~ADY, Jozaef
polyoxy-chromoneg. IV. S7nthggis of isocaviunin. Ylagy kem folyoir 68
no.lig-ii Ja 162.
1. Budapelsti Mwzaki rgyetem Szerves-Komiai Tanszeke-
(ChromDng) (Caviunin)

FARKAS Lorand- VARADY, Joamef
I
Ring lemrftatlcm-of isoflavonea.V.Pinal structure of
cavign%F W"thesis of 7-methyl-caviunin. Magy kem folvoir
68 no.3:93-~.94 Mr 162.
1. BtdmVwttiMamk:L Effetem Szerves-Kemiai Tanazeke

.FARK.AS, Lorand; VARADY, Jozsef
Ring isomerization of isoflavones. Magy kem folioir 68 no.6t
237-218 Ju 162.
1. Budapesti Massaki Egyetem Szerves-Kemiai Tanazeke.

FAPJW, Lorand; VARADY, Joasef; GOTTSEGEN, Agnes
Ring isomerization of isoflavonse.VII.Synthesis of 41-methyl-
tectoriganin. Magy ken folyoir 68 no.6s238-240 Je '62.
1. Budapesti Mussaki Igyetem Swrves-Neslai Tansmake.

FODOR, Gabor, akademikus; BERE, Denesne; BITE, Pal, kandidatus; DOBO, Pal;
XA9NAa4_L ERT, Karoly,, kandidatus;
graUt....Jandidatuo; F. VARGA., Eva; MIPE
MVQB-#. I&azlop kandidatus; SZAIJTAY, Csabap kandidatus; UMCH, Ferene
An account of the Prague Symposium on Natural Organic Compounds.
Kem tud kozl MTA 19 no-1:95-103 '63.
1. Magyar Tudomanyoo Akademia Sztereokemiai Kutato Csoportja.,
Budapest (for Fodor, Beke; Lempert,, Otvos, Uresch). 2. Magyar
Tudomanyoo Akademia Kemiai Tudoinanyok Osztalya (for Bite, Dobo,
Farkasp F. Varga, 3zantay), 3, "A Magyar Tudomanyos Akademia
Kerliai Tudomanyok Osztalyanak Kozlemcnyei" szerkeszto bi-2ottsagi
tagja (for Fodor).

FARKAS, Lorand, dr.j VARADY, Jozoef
-----------
Polyaxychromone. IV. Acts, chimica Hung 33 no.21l79-182 162.
1. Institut fur Organische Chemie dom Techaischen Universitat,
Budapest, XI., Gellert tar 4.

FARM, Lorand,, a kemW tud=Lnyok kandidatusa
Natural isoflavones and their glyaosideso, Ken tud kosl t
MTA 19 no.2:213-219 163.
1e Budaposti Mussaki Egystem Sserves Kemiai Intesete,

-ran'" I.-AJI 0-:) - IS Tq:
y;oa-' LP _`!-.Y, lanoo; Teeh.-,olo.-ical Uni%re=4ty
AL Xn,
of 3-udaoes-'k,, Diaixaft-rient of Orl:7anic Chen.4 stry (Budapesti ~'u j'7,k4
"i2erves-Kemizi Tanszek5-
"Rin!-, Isomerization of Flavones, 1. Conversion of 7-I"'ethyl Vo,~Onin into
7_XeIk-Ihyl Oroxylin.
Budapest, Ma"ar Kemiai Folyoirat, Vol 69, 1'~I'o 8, Au.,- 19'3,
Abstract: [Authors' Hungarian sm-aary] The benzyl derivative of 5-hydrovj_
?,8-dime-uhoxy-flavone, 5-benzylocy-7,8-dimethoyy---rllvone, react3 ~-'ith
potassium ethylate to form 2-hydro-.%y-2,4-dimethoxy-o-benzylocy-d~-l'-v,~rzoyl-
methane. This compound, on catalytic debenzylation and subsequent heatin'7
in vacuo,loses water and the product, 5-hydroxy-6,?-d:LTc-tiio..:y-flavone,
that is, 7-methyl-oroxylin A is obtained. All 'dostern referencez;.
1/1

FARKAS, IOrandj VARAI)y, jozaef; GOTjSErEjj Agries
'.. ~. ~~ ~, -, _4 -,--Al- pt.8. 14agy ken folyoir
Ring isomerization of iSO-flavOneso
69 no-10:458-460 0 163.
Ring isomerization of iso-flavones. Pt.9-460-462.
1. Budapeoti Munzaki Egyetem Szerves-Keiniai Tanazeke.

FARKAS, Lorand; VARADY, Jozeef; GOTTSEGER, Agnes; KENGYEL, Vilma
Research on Baptisia tinctoria R.Dr. glyaosides. Pt.2.
Magy kem folyoir 69,no.10:"8-450 0 163.
1. Budapesti Muezaki Egyetem Szerves-Kemiai Tanszeke.

PALLOS, lqszlo (BiidnnP--t, XI., Gellert ter 4); FARKAS, Lorand, dr. (Budapest,
XI., Gellert ttr 4)
Aurones and their glycosides. Pt.5. Periodica, polytechn chem
8 no.31l83-189 164.
1. CI-tir of Organic Chemistry of Budapest TachnicnI University,
and United Drug and Nutriment Factory, Budapest. Submitted
February 6, 1964.

ERDEY-GRUTZ) Tibor, akademikus; BRIJCKNER, Gyozo, akademikus; VAF.GHA , Ia-zlo;
KORACH j Mor, akadem-ikus; FREUVT, Mihaly, akademikus; FODOR, Gabor,
akademikus; GEREGS, Arpadp akademikus; SCHAY, Geza, akademikus;
BITE,, Pal, kandidatus; BOGNAR, Rezso, akademikus; FARKkS,"Lorand,
kandidatus
An account of the work of the Section of Chemical Sciences, Hungarian
Academy of Sciences. Kem tud kozl MTA 22 no.2:109-152. 164.
1. Secretary, Section of Chemical Sciences, Hungarian Academy of
Sciences, and Editor, "A Magyar Tudomanyos Akademia Kemiai Tudomanyok
0aztalyanak Kozlemenyei", Budapest (for Erdey-Gruz). 2. Editorial
board member, "A Magyar Tudomanyos Akademia Kemiai Ti-domanyok
Osztr;:lyanak Kozlemenyeill (for Bruckner, Korach, Freund, Fodor,
Gerecs, Schay and Bognar)- 3. Corresponding member, Hungarian
Academy of Sciences, and Editorial board member, "A Magyar
Tudomanyos Akademia. Kemiai Tudomanyok 0sztalyanak Kozlernenyei"
(for Vargha).

FARFAS, Lorand, u:-.
Complet#,:, of phyoclonlno. A.Cta- chinica Hung 40 no.3:
309-315 Ic,4.
1. 1riatitut, der Tlf~jchnl Lichen UnIvrrgitat,
Budtq,o-.L, (1 , , Gellert Ler.4.

FARW Lorands dr.; VMADY, Jozaef; GOTTSEGEN, Agnes (Miss)
Data,on the ring isomerization of isoflavones. Pt.10. Acta
chimica Hung 40 no.41457-461 164.
1. Institut fur Organische Chemie der Technischen Universitat,
Budapest, XI., Gellert ter 4.

FARKAS, Lorand, dr.
11
Ioolation of luteoline-7-glucomide from Achillea millefolium
L. and a new synthesis of this glucoside. Acta chimica Hung
40 no.4t463-469 164.
1. Inatitut fur Organische Chemis der TechnIschen Universitat,
Budapest, XI., Gellert ter 4.

Lorano, dr. (bUlapsist., P., C-Ilcr';
(ftem"'Wit, 'XI. Cjtll,)rt ter 4.~ t:
Xi., GbIlsirt ter 4)
Data on the ring isom6rilzF-tion ef
161
chimica Hwg 41 no.49441-1,44 0
1. Inbf;!tu'. fur Organianhe (,hem-1cl ie.- tat
Budapest.

OITI(, r
no.
ntry,
--�rl",

FARKAS, Lorand
Structural determination and synthesis of one of the glucosides
of Rheum palmatuiR var. tangut. Magy kem fo-lyoir 70 no.9:390-
392 S 164.
Synthesis and isolation of luteolin-glucoside (7) from
Achilles. millefoli= L, Ibid.092-394
1. Chair of Organic Chemistry, Budapest Technical University.

FARKAS, Lorand; MAJOR, Adam
Acylation of active methyleno groups. Pt-3- Magy kem folyoIr
70 no.10:421-422 0 164.
1. Chair of Organic Chemistry, Budapest Technical University.

FARWAS, Lorand
Synthesis of casticin. Magy kem fol)roir 70 no.10,,441-
442 0 164.
1. Chair of Organic Chemistryp Budapest Technical Uuf-vz~-j--.ty0

~~4RKAS, _Lorand, dr. (Budapest, XI., Grellert ter 4'); WRADY, Jozsef (budape-st,
X-I-.-,IGellert ter 4); MAJOR, Adam (Budapn3t, XI., Gellert ter 4);
GOMEGEN, Agnes (Budapest, XI., Gellert ter 4); !;TWE-1,1,7IY, Janos
(Budapest, XI., Gellert ter 4)
Ring Isomerization of flavones and isoflavones by means of potassium
etbYlate. Perlodica polytechn chem 8 no.3:177-182 '64.
1. Chair of Organic Chemistry of Biidapest Technical University.
Submitted February 6, 1964.

L 63729-65 RM
ACCESSION UR: kT5M2241 EIU/2502/64/0041/0004/044l/olA4
AUTHOR: Farkas Lor Its)(Doctor)(Budapest); Varadyj Jozsef(Varadij.)
~qk_ _ aj4(Farkash,
(Doc tor)tBUI-a-p-e-sT7,~-W-tVse-gen, Agnes(Budapost)
TITLE: Ring isomerization, of isoflayones. Part II. A new synthesis of 7-methyl-
tecturigenine
SOURM Academiae scientiarum hungaricae. Acta chimica, v. 41, no. 4, 1964, 441-
444
TOPIC TAGS- crystal, isomerization, ketone
ABSTRACT: The synthesis of 5, 41 -di ydroxy-6.7-dimethoxyisoflavone*(7-methyltecoI
h
torigenine, found in the flower of Dalbergia als-do o_)by_ po~a=sum7ethylate- induced
ring isomerization of 5,4'-dihydroxy-7, 8-dimethoxy-isoflavone was described. The
ethanol-soluble product has a melting point of 226-227OC; it forma light-yellow-
colored need~e-shaped crystals.Orig. art. has: 2 figures.
ASSOCIATION: Institut fur Organische Chemia der Technischen Universitat-f Budapest
(Institute for Organic Chemistry at the Tecbuical University)
I.-Card. 112

3729-65
6
L
ACCESSION UR: AT50M4
SMMITTED: 18Feb64
M REF SOV 1 000
ENCL: 00
OTM.- )008
Card 2-12

L 63691-65 E'dP(J) RM
A-CCMS1014 IMI MoaaAa HU/2502/64/0041/0004/0445/0449
AUTHOR, Farkas, Lorand (FarkaakiL.)(Doctor)(Budapeat); Kajor, Ad (Kayor, A..)
(Budapest
TITLE: Acylation of active methylene groups. Part 31 Extension of the gattermK6 --cl,
synthesis of tri- and tatrehFdroxyphenyl benzyl ketones
SOURCE: Academiae scientiarum hungaricae'.-Acta chimica, 41, no.4, 196.41
445-449
TOPIC TAGS: ketonelchemicalreaction
ABSTRACT-.-2,4,5,6-tatrahydroxyphenyI benzylketone and 2, 4, 6-trihydroxyphenyl
benzylketone were formulated with.zinc cyanide and hydrochloric acid in the,
nucleus. In the tetrahydroxy compoundt foruqlatiod occurred in the alpha position
with respect to the ketone group, - Orig. art. has'. 3 figures.
ASSOCIATION- Institut fur Organiache Chemie der Technischen Universitat,Bu4apest
(Institute ior Organic Chemistry at the Technical UtLiveraity)
Card 112

JJ -i
L 61691-65
fm:
SUMITM- 22Apr64 ENCLt 00 SUB CODE-. OC,OC
NR RM SM 000 07='. 013 JPM

L 3277-M
H
5W64~- b4Zft4-A393/0393
U/2
AUMORt LarkM,, Iorang (Doctor)(Budapeet)l Najors Adam (BuUpost): Vermeal
BorbaU
TITUt Studied on the glucasides of acacetine. Part Is SynthesIA Of tiumnimt
a f1avone-Aucoside of TJ I I a Japonica SimoWmi
SOURCE: Academia ecient4aru- hungaricaeo Acta chindca# re 42l noo 49 1%41 393.
r
395
TOPIC T&GS: carbohydratet organic synthetic process
Abstract: Orman. i Lei' Ythe Btu'-Co*side 66iur*rLn'g to Tilla lai)onica
t
Simonkai, tilianine,, was synthesixed with the *in of establishing Its
structure. The synthesis was accomplished through the preparation of
scaestine-7-0-D-glucoside-pentaseetsto (tillanine pentascetate). The
.product wis-identified by'asans of the synthesis,, and by comparing its'
ultraviolet spectra with thosc-of the natural material, as
5j7-dLhydroxy-41-oatboxyflavons-7-0-D-alucooLds, with a malting point..'
of 259-262*C* " "The* -jj'tji-94~~'Aademq of
J&iit6iie f6i-the support of this vork and Chemist I& Balog-Batta for her
so mplishiment of the micro andlywiso" Orige arto his 1. formula.

FLRKA.S, Lorand; MAJOR, Adam; Borbala
Analysis of the glycosides of acacetin. Pt. 1. Magy kem folyoir
71 no.3:98-99 Mr 165.
1. Chair of Organic Chemistry of Budapest Technical University.
Sutmitted June 22, 1964.

FARPLL-, LcranJ; N031*01 1,11haly
I Y
Ramark-q about the 0trUCt[;l-r; Of and zrApotinin. Pt. 1.
Magy kem foJyotr '71 nn.'3:'l3-,'.-135 Mr 165.
2. Chair of Orgariic Chemi.,.,try of Budapest Technical University.
Submitted July .1.5, 196"10

--------- ----
L 01186-66
:ACCESSION NR: AP3025819---
!AUTHOR: Farkas,* Lorand; Pallas, Lasslol Nogredi, MUmay
TITIZ: Aurones and aurone gluoosidese Part 8: Synthesis or naritimins, one of
the glucosides in Coreopsis mritima
SOURCE: Magyar keNdAki f02y0ir9t. V. n, Do. 6, 1965, 270-M
iTOPIC TAGS: carbobydrate. plant chemista7. organic synthaUe process
,ABSTRACT.- (part 7 of this series was published In M"ga MdkP
1964' P 2961 6..7-dihydrfty-2-(3.4-dihydranybenul)t'CUift;WC3 .0'
D-glucoside-(6), proven to be identical with oas of the gb1cosides in
201:-980)t was "athe-
t: 207-20SOC; I&D
CqXeggli =ritim2(selting poin
etzed iq9thef coAde6ation of G...-7-dihydroxy BIUCAGids
lehyde -In m6stlc ride followed-by "Pon"t-
with protocatechol al~
cation. Orige ar~'ffi-haa: e
ASSOCIATION: Mazald EVOtAx Sserves-Kemial Tansmakel, Balffest (Departmut of:~.
Organic Chemixtr7 at the Teabn1cal 11niversi1r)
SUBMITTEDt lvtl)so64 EM14 00
.30 CWB: CC. IS
NR REF SOVt 000
009
~15

L 01185-66
ACCESSION NRt AP5025820'
AUTHORs Fark"t,10randl Pallos, Lasslo; Hogradi, Miha3y
TIT12: Aurones and aurone glucosidese Part9s A now synthesis of Idptosine
SOURCE: Magyar kemiai folyoirat, vo 71, noe 6. 1965. 272-273
TOPIC TAGSi carbohydrate, plant chemistry, organic synthetic process
ABSTRACT: 6-bydroxy-7-notlioxy-2-(3,4-dihydroxybetkzal)-cumaranane-(3)-
I -0-D-glucoside-(6)s proven to be identical.with leptosine, one of the
glucosides ii% GorjoR#Lp,&X&nd~flgr&.W .., was 'synthatized from
6-hydroxy-7-mathoky4vairadona;-(3)-P;-u-giucaside-(6)-tatr"catate
by condensation with prok6catecholaldehyde. in acetic anhydride, fol-
lowed by saponification. The product had a metting point of 235-23VC-61
'-ik. ham' fo
0
rige
t
ASSOCIATION: HusrAki. Egyetex Starves-Keniai. Tanstake, Budap~st (Department. of
;Organic Chemistry atthe1schnical University)-
iSUBMITrEDt 17Deo64 ENCLt 00 SUB CODKt GC, IS
,NR REF SOV: 000 OTHERI JPRS
~-Card 1/1

AUM I Pmv-1-mr., tornnd; Major, Adam; No.rrsdi, 11haly
CRG: Department of Organto Chemistry. Phkinpe.-jt Trochnological UnIversity, DWapest
(BW&pnsti Masaid %y*Un 3serves-Kemial Tanssake)
TITUs Synthesis of two d1hydrochaloone S;=oWes from Malus trilobata and He
sieboldil arboresomm
SOURCKs Xaffw lanial, folycirst, Y, 71. no. 11, 196.5, 477-479
TOPIC TAGS: organic synthetic process. bydrogenation, bydrolysis, plant chemistry
ABsT.jAcT. Catalytical, hydrogenation of the chalcome obtained from 2-bensoyl-
:.phloivacetophonon-4-0~-D~-glucoside and. p-hydroxybenzaldehyde gave phloratin-
:41-p'D-glucoside. This was identical with the dihydrochalcons isolated from
,Malus trilobata. Partial bydrolysis of 3-hydroxyphloretin-21,41-di-p-D-
glucoside yielded 3-hydlvxyphloratin-41-A-D-glucoside, identpal with the
dihydroohalcocs Isolated from Malus sisboldii, arborespens. I.JFRSt 33,0-67'
SUB CODE: 07, 06 / SUEM UTE t 17W65 OTIE REF 1 013
Card 1/1 Vrb
7e,

MKASO L,G., HUDr
Surgtcal spithalization In burnn. CAD.lek.cank. 91 no.41:1177-1183
10 Oct 52.
1. Z kliniky plastickej chimrgle K.U. v nemocnial na Kral. Tina-
hradoch.
(Buns, surgor.7.
spithellmation)

FARXA , L.G. - DOLVZAWVA, J.
Surgical difficulties in bypospadias. MIeff. sebeezet 7 no-5:
361-370 Oct 54.
1. A.3ragal PlaeztDc&JL Sebessett Klinika (igazgato: dr. F.Burian
prof kazlemenys.
(HYPOSPADIAS, surg.
urethroplany)
(URETHRA, surg.
plastic in bypospadiam)

FARKLS, L.G., MUDr
Oonservative and surgical treatment of chronic skin defects. Roshl.
ohir. 33 no.1:4-11 Jan 54.
1. Z kUniky plastickeJ ohirurgle v nemocnict na Kralovskych
Vinohradech
(SKIN, wounds and Injuries,
surg. & ther.)
(WOUNDS AND INJURIBS,
skin. surg. & ther.)

FARKAS, L.G.
Dermo-spiderml graft In the hands of a surgeon. Bratisl. Isk.
listy 34 no.2:189-195 7 154a
1 Z K11nHW pLotickaj chirurgle Karlovaj university, prednosta
prof, dr. Yr.Darian,
(all TUNSPLARTATION9
*derm-spIderma cWts)

EXCERPTA MEDICA See 12 Vol"13/4 Ophthalmology Apr 59
609. EXPERIENCES OP THE CLINIC FOR PLASTIC SURGERY IN PRAGUE
wrril THE TREATMENT OF CONGENITAL PTOSIS BY THE METHOD
OF REESE-BURIAN - Zkulenosti kliniky Plastickd Chirurgie v Praze s
166bou vrozend ptosy videk metodou Re esovou -Burt anovou - F a r k a 9 L.
Fdra M. and SedId6ek J. Klin. Plast. Chir. a O6n6Ei_n..Ilyg.
Fak., Karlovy Univ., Praha - 6SL.OFTHAL. 1958, 14/4 (283-290)
Illus. 3
Sixty-one patients were operated on from 1936 through July 1957 at the clinic
mentioned above. The method was used In 26 cases and showed very good results
in 18 patients, favourable in 7. The remaining patient could not be controlled.
The advantages of this method can be summarized as: the surgical procedure is
simple and of short duration; it does not interfere with the anatomical structure
of the eyelid; it makes a natural and proportional raising of the eyelid possible;
it shortens simultaneousIv the skin and the orbicularis, the postoperative scars
are hardly visible; it does not preclude the possibility of further corrective oper-
ations, if necessary.
Zahn Prague (XII, 19*)

EXCH(PTA 3ec 9 *101 1311 Surgery Jan 59
277. CORRECTIVE OPERATION ON THE LIP AND NOSE - Korektivni
operace rtu a nosu - Fa rkaA L. G. and Stockar B. Klin. Plant.
Chir. KU, Praha X11 - ACTA CHIR.-ORTHOP. TRAUM. CECH. 1958,
25/1 (43-53) Illus. 40
The authors have reviewed material from 666 patients with deformation of the lip
and none from clefts, in whom a corrective operation was carried out at the
plastic surgery clinic in Prague from 1946 to 1956. The operative technique is
concisely described for the most common forms of deformity of the lip and nose
from cleft palate. Good results after corrective operation were attained in about
50% of the patients, very good results in more than 33%. (D(. 19*)
Ali

STOCKAR, B.; )%NW, L.G.
Secondary operations in cleft palate. Acta chir. orthop. tramm. coch.
23 no.1-.54-62 Feb 58,
l' Klinika plasticke chirurgis SU v Press XII, prednosta. akadmik
P: Burian.
(OLVI PAJAM swg.
secondary surg. (0s))

FARKAS, L.G.; KMZ&K, R.
Avulsion of the skin from the penis and scrotum. Acta chir. orthop,
traum. each. 26 no.4.-312-318 Aug 59.
1, Kliulka plastloke chirurgle v Praze, prednosta akademik F. Barlan.
(SCROWN, wds & inj. ) (PENIS, wds A inj. )

(-I I
-- FARKASL.; XARA, H.
Role of skin imnlantg in plastic BUrgery. Acta chir. orthop. traum.
each. 26 no-4:319-327 Ana 59.
1. Klinika plastiak~ Chirurgie byglenicke fakultY 11arlovy University
v Praze 12, prednosta akademik Yr. 'Barian,
(SKIN TYANSPIWMTION)

BURIAN,Y.; FARAL,M.; FARWtL.
Pyamorphia Orbitopalpebralis Congenita. Acta chir. plant. 2
no.1-1-11 16o.
1. Glinia of Plastic Surgery, Gharles University, Prague
Oxechoslovskla), Director:.Academician 1. Burian.
WIMIS abnorm. )
(ORBIT abnora. )

FARIAS,L.; FARk.M.
----------
The surgical treatment of congenital blepharoptosis by means
of corium wascle flaps. Acta chir. plast. 2 no.1:12-17,60.
I
1. Clinic.of Plast,to Surgery. Charles University, Prague
(G2~choslovafcI&-). Director: Academician Ir. burian.
(273LIMS abnors. )

PARKAS, L. ; FABA, M.
Skin grafts of the orbit. Act& chir. pl&st. 2 no.1:52-58 160.
1. Clinic of Plastic fnwgory. Charles University, Prague
(Osechoslovak4a), Director: Acadesiolan F. Burian.
(OBBIT surg.)
(SKIN THMPIANTATION )

FAFXAS, L.G., MUDr.; KLASKOVA, 0.1 MUDr.
Mrperienceo with a key questionnaire in research work. Cesk.
zdrav. 11 no.12:514-516 W63.
1. Iaborator plasticke chirurgie CS&T,, Praha.

MRIANY F., academician; KLASKOVA, G
'7 AL CMIMMA, J.
Qaestionnaire for resea2ch on the etiology of cleft-lip
and cleft palate and other congenital malformations. Acts.
chir. plast. (Praha) 6 no.2t88-113 164
1. Laboratory for Plastic Surgery# Czechoslovak Academy of
Sciences, Prague (Czechoslovakia)IDirector: Academician
F. Wrian.

SAS, M., dr.; FARKAS, M., dr.; SZEGVARI, M., dr.
Treatment of the menopause with a/,preparation of estrogen-angrogen
combination. Ther. hung. 10 no.3 :14-18 162.
1. Gyrfiecqlogical Clinic (Directors Prof. F. Szontagh) of the Medical
Univeraity. Szeged (Hungary).
(MENbPAUSE) (ANDROGENS) (ESTROGENS)

HUNGARY
FARKAS, Marton., Dr, RAK, Kalman, Dr; Medical University of Szeged,
-Obstetrical and Gynecological Clinic and I. Medical Clinic (Szegedi
Orvostudomanyi. Egyetem, Szuleszeti es Nogyogyaszati Klinika es I.
Belklinika).
"Hemorrhages of Thrombocy-topathic Origin."
Budapest, Orvosi Hetilap, Vol 104, No 22, 2 June 63, pages 1016-1019.
Abstract: [Authors' Hungarian summary] Two sisters suffering from
thrombopathy experienced severe hemorrhages during abortus and deliv-
ery. The hemorrhage during delivery was especially difficult to
control and after a long and unsuccessful conservative treatment,
hysterectomy had to be performed. After a summary on the physiological
role of the thrombocytes, the biochemical aspects of the pathological
blood platelet function, the classification and terminology of thrombo-
cytopathies as well as methods of treatment are discussed. 15 Western,
3 Hungarian references.
J
M

FARKAS~ Marton) dr.; RAX, Kalmn, dr.
On thrombocytopathic hemorrhagic diathesia. (Gynecological hemorrhagic
complications in familial. thrombopathy). Orv. hetil. 104 no.22:1016-
loig 2 je 63.
1. Ssegedi Orvostudomanyi. Egyetem, Ssuleszeti, es Nogyogyaszati
Klinika es I. Belklinika,.
(THROMBOCYTOPATHY) (UTERINE HEMORRHAGE) (POSTPARTUM HEMORBRAGE)
(ABORTION 9 THERIFEUTIC) (BLOOD TRANSFUSION) (HYSTERECTOIff)
(AMINOBALICWG ACID) I

COSMAY V.,, dr.; FODOR, 0., prof., MUNTEANU, P., dr.; SCHWARTZ, M., dr.;
MEDREh, B. dr.; ERDOSY, St., dr.; BADEA. Gh., dr.; in cola-
borare cu: FORGAGS., V.dr.; GRACIUII. I., dr.;-F-ARKAS, M.dr.
Research on several digestive diseases in an occupational
lead-poisoning environment (ulcer disease and epidemic
hepatitis). Med. intern. 16 no.2:221-228 F164.
1. Clinica a III-a medicala I.M.F.,, Cluj (for Cosma. Fodor,
Munteanu., Schwartz, Medrea, Erdosy Badea). 2. Dispensaral
Uzinelor metalo-chimice,, Maia Mare (for Forgacs, Craciun,
Farkas).

FARKAS, Margit
DeterminatIon of coal and hydrogen content by the lamp method.
Veszprom #agyip egy kozl 4 no.41305-306 160
1. Peasi Orvoetudomanyi Egyetem Kemiai Inteaete.
.1

HUNGARY
FARKASM M . -tedical University of Pecs, Institute of Pathophysiology
(Pecsi Ao-Astatomanyi. Egyatem, Korellettani Intezet)*
"The Effect of Thyroxine, Cortisone and Exposure to Cold on the Liver
.ycogen Level"
GI
Budapest, Acts, Physiologica Academiae Scientiarum Hungaricae, Vol XXX,
No 1. 1966, pages 31-38-
Abstract: ZE-nglish article, author's English summar7 modifieg In a cold
environment, there was a temporary decrease in the liver glycogen contebt
followed by an increase approaching the normal value. The liver glycogen
content remained low throughout chronic thyroxine treatment. The decrease
in the liver glycogen content caused by thyroxine was blocked by cortisone
at room temperature but not in a cold environment. The weight of the liver
increased to a considerably greater extent in response to cortisone than
in response to thyroxine of cold. The reduction in liver glycogen content
by thyroxine and by cold is caused by different mechanisms and the effect of
cortisone on the liver glycogen content is dependent, to a large extent, on
the environmental temperature. 2 Hungarian, 22 Western references. 5-1~u-
script received 12 Aug 65.7
1/1

~M,
I NGARY
FAW6, Maria, XOZSA, Szabolcs, and DOROFFSR, Szilard, Institute of Patho-
pE-ysli-~I~o~',-Vhivemity Medical School (orvostudo-many Egyetem Korolettani
Intezeto), Pecs.
"The Effect of Fypoxic ;~rpoxia and Environmental Tem.peraturo on Body Temporatu
and Oxygen Consumption in the Course of Pyrogen-Induced Fever"
Budapest, Acta Physiologica Academiae Scientiarum, Hungaricae, Vol 30, ,,'a 2.
1966; pp 155-159.
Abstract [Article in English; authors' -Wnglish swmrary]: At ambient tomporatur
below the themoneutral zone of the normal rat, the response to hypoxia
(breathing 12% oxygen) was the same in the animal witiO. pyrogen-induced fever
as in the untreated animal; oxygen consumption fell and deep body temperature
declined. At an ambiont temperature corresponding to the Jndifferent tempe-
rature of the untreated rat, however, oxygen conswnption increased and deep
body temperature declined in pyrogen-i-nd-aced favor, whereas both oxygen can-
sumption and body temperature increased in the untreated animal. The bearing.
of those results on the relationship of thermoregulatory responses and of the
response to hypoxia is discussed. 6 References, of which 4 by Fungarian autho
(3 of these in iiungarian journal). (Manuscript received 15 Oct 65).
1/1

FARKAS, Marianne; MDORM' CSANn, Piroska
Determination of the lead-tetraethyl content of benzine
by the absorption of the retardation radiation of tritium.
Magy kem folyoir 69 no.9:407-409 S 163.
1. Eotvos Lorand Tudomanyegyetem Fizikai-Kemiai es
Radiologiai Tanszeke, Budapest; Elektrokemiai Akadevilai
Kutato Csoport.

DCMHOYM. Sz.; VARNAI. Ilona; SZEGVARI, Gy.; YAJUW, Varia; JARAI.I.
Paper chrovAtographic and pisper electrophorstic analysis of
iodothyronine and dtiodotyromine preparationa. Act& physiolo
bung. 17 no.3:251-264 T60.
Institute of PhathoptWalology, Nedical Univeraity. Face.
(WROSITZ chem) (THYR(NM chem)

FARKAS, M.
'Hilbert spaces with kernel function' by H. Memchkowski.
Reviewed by M. Farkas. Periodic& polytechn electr 7 no.2:
168-169 163-

FARKAS, Maria
Aqtivities of t~e Scientific Association for the Agricultural
"d Food Industries at the Kapoavar Sugar Factory. Cukor 11
no.5:127 MY158

SILBERG, A.j SIMITI, I*; FARKAS, 14,;.SILBERG, S.; MANTSCB, B.
Contributions to the study of thiazoles. Rev chimie 7
no. 1: 513-519 162.
1. Medizinisch-Pharmazeutisches Institut, Laboratorium
fur organische Chemie der Fakultat fur Pharmaziep
Cluj.

11.1
FARKAS, Ribaly
Import-export problema of the heavy ourrent industry.
Elektrotechnika 52 no.2/2:52-58 I,59*
1. A THAISELEKTRO foooztalyvesetoje.

FABERj, Miklos; FAPJLAS,, Mihaly
mounting Of ths Elizabeth Bridge.
6 Je 16.3. Nilsz elet 18 no,12:1.,,Io

FARKAS, Mikulas, inzo
Terrain repreBentation on a map. Good kart obzor 8 no.9:176-179
s s62.
1. Kartograficky a reprodWwni ustav, HDdra-Harmonia.

k
lm";*i
!U9m6w&j mu=&, X.
.SOPsimp abdoximl lMhO9raWA1OffAtosjg bY Pannyalopathy,
OrT. hetil. 92 no.2t56-5? 14 jan 1951, Si=latsd NINL 24:2)
1e' Doctors. 2. Internal Clinic (Director -- ]Pror. Dr. Janos Angyan)
and Institute or Patholoa.0grector - Pror. Dr. Bola lints) of pace
University.