SCIENTIFIC ABSTRACT HAHN, V. - HAIDUC, I.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R000617810019-8
• Release Decision: RIFPUB
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: January 4, 2017
• Sequence Number: 19
• Publication Date: December 31, 1967
• Content Type: SCIENCEAB

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tuG0 :,

(~5.-I. 25, 4100) to a mixt. o[ the �orrc~ondl.g amln~ll-;
phctiyl ell]ets, bt1 ISO~t~s, tn 75% yield, which were
ruled ~o the hMividmtt ethe~ by Suter's meth~ (toe. Hr.).

quin,Jliae (Ii) purlfic,l by ~:cuum dktillu,tlon; b,t D18:-22'. - .
m. 11~5.~L5% ILtICI c~'stailla~ fmsR I~tOH-~t:O ~ the.

lYb. gave HI,,,, Rt. 17~1~;~ ' pkrdte,' yelloiv- needle,' ' m. �
m. 175--5.5~ (d,~,mim-) (ftont l;tOi[~ik.y~tue). To 0.~
mole 1[ in l{~l mi. hat, :th.{. ELOII .~',{s ~Idcd 0.1t52
Na -Y;'r i,~d {,,a~r, Iii) ml. ,{or_: El Of [ 'a',ul added t,, dhsolv�

/

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/ � w ' ' I i. x Ii; .. ' ......

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;l ":i':' .l;;?:..:: %: d;l ': I1~
- ' "_'.,..._ '- :: - - -

.- _ L ~; :2/_.- ;:-� -. ~ :. c. '. -'.' '~,~-i': '.
. ' -::

: ' - ' .~-~s ~t~ off, dhmlv~ L5 28 ml' }[.o I,' ~,..a ..... -,'
pm~ from tile K ~llt with BaC' '

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~C['[CI, w~l~ added ~)owl~ ivith slirring {o a suln. el 6 g. ~-~"
tfuranUide in Il0 I~, CllCll, I. he mJxl. reflitxud ,10

and filtered hot lo give, urt~ t~,lll&g, d..t g.'~-bromoanilide
(I) c~ ~?oml~2-htruic ueld m. 1.12-8"; ulmlyll~l ~ml,I~-,
,n. 101 u�(fromEtOt{)~ Anlixt,of2'i. lalu1251{ll,i:t,llcll.

, wa~ llbtainud [mill ](tmO ~hl.),- thc aq. ~111. wa; fillclcd.
excc~ NaOl{ mhlcd, thc mJxi. oxid. w{ik ElmO,
[ ~,ln. drkd, evapd., thu resMue ,lii~,lvcll ill ll~O, I]ltc~cd
NnOl[ ~oln. added,' Io yield ~rCslliNllt'(ll).
: 2-[uroyl chloride (0.3 g.) ~ 15 mi. C, II, was d/op~d iuh)
g. II in 15 mi. C~I,N, the mixt. r~ux~ 30 miu.. hehl
:hrs. at r~nu letup,, 15 mL C~[{{ a~ld 20 mi, H:O athirst,

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A~s Joust : Ref Zhu~ - Biol.~ ~o 3~ 1358~ 12718

Author

Inst

Title

0rig Pub : Acta pharm~c. Jugosl., 1956, 6, No l, 27~32

Abstract :

Card 1/2

A study was made of 4 N-acyl-urethans: N-carbetho~
succinoamide (I), N-carbethoxysuccindiam~de (II), N-
carbetho~yphthal~mfde (III)~ and N-carbetho~ccharine
(IV). I, III and IV were obtained by usual methods
slightly modified (E~ller~ O., Jacobsohn~ P., Ber.~ 1921,
54, 1107; Eckenroth, E., Eoerppen, G., Bet., 1897~ 30,
1265). II was obtained by the action of an excess of a
25% aqueous solution of ammonia upon I. Toxicity of the

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~UGOSL~.VIA/Or~nic Chemistry .~ S~'_,theti20rg~ni.n ~emistry.
Abs Jour ~ Ref Zhur ~. ~himiy~.~ No 7, 1~58, 21~72

G-2

Author
Inst
Title

0rig Pub

V. Eahn, No Pr~vdio-.Bla~o",ric.

The 1~'eparation of Some 1-!~nitrophenyl)-.R-p~ridones and
o.thiopyridones �

Croat. chem. acta~ 1957, 2~ No 2~ 127-1~9

Abstract

Card

1-(3',,nitrophenyl),-R-pyridone (I) and 1-,(4'-nitrophenyl),-
-~.-pyridone (II) were sy~.thetizedand the corresponding
2-thiopyridones (iii and IV) were obtained from them.
Pyridone-2 is prepared of O.lmole of 2-aminopyridine in
100 mlit of 20~.uel HRS0~ by the action of 0.106 mole of
NAN02, yield 75~, e~nd it is transformed into ~e K deri-
vative (V) according to Binz and Raeth (Liebigs Ann.
Chem., 1931, 489, 107); V is a monohydrate, melting
point 269 to 273�. 45 mmole~ of ~hydrous V, 180m~ole
of m~,BrC6H~N02 and 0.3 g of Cu powder are heated h hours

~c~Sl$l~l~~ $($1~ �L~S ~YI~�7/~i� c~%~6P86-OOS 1�~-000617810019-8'
Abs Jour : Ref Zhur ~, Khimiya, ~o 7, ~958, 21~7a

at a40 to 260�, distilledwith steam and I is extracted
with water from the residue, yield 63~, melting point 18~
to 185� Iifrom alcohol), l0 mmoles of P2S5 is added to l0
mmoles of I in l0 mlit of anhydrous CsH5N, all is poured
out into 50 ~lit of water and III is ~eparated (at about
0% 12 hours), yield 84~, melting point 199 to ~00�
(from benzene)� II was prepared of anhydrous V and
n-C1C6H4NO2 similarly to I, yield 50~ melting point 188

to 189� (~rom sd.aohol); Y~_was prepared similarly to III~
yield ?]5~ melting point 17~ to 175� (from behzene).

Card 2/2

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HAmt, V. (Zagreb); KUKOLJA, S. (Zagreb)
Studies on 4-pyronos and 4-pyridonos. I. The proparation
of 1-aryl-3-hydr�xy-4-Pyrid�nes and related compounds.
Croat chem acta 33 no.3:137-144 '61.
1. Laboratory of Organic Chemistry, Faculty of Teclmology,
University of Zagreb, Zagreb, Croatia, Yugoslavia.
2. t.~mber of the Editorial Board, ,,Croatica chemica acta,
Arkiv za kemiJu" (for Kukolja). '

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KUKOLJA~ $.} H~J{N,. V.

Studies oa i-pyrones and 4-pyridones.
rearrangement of ]-a11~loxy-A-p~rone.
229-233 '61.

II. The preparation and
Croat chem acta 33 no.4:

1. Laboratory of Organic Chemistry, Faculty of Technology,
Univeraityof Zagreb, Zagreb, Croatia, Yugoslavia. 2. Clan
Redakcionog odbora, 'Croatica chemica acta' (for KukolJa).

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PRAVDIC

, N.; HAI*I~ V.

Contributions to the knowledge of the n~mides of thiocinnnm~c
acid. Thionmtde. Note II. Croat chem acta 34 no.2:85-88 '62.

1. OdJel biokemiJe, Institut "Ruder Boskovicw, Zagreb, i
Zavod za-organsku kemiJu~ Tehnoloski fakult~t~ Zagreb.

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}5%HN, Witold E.; KoTaOWSF~A-~I~EJA, Zofla

Hy~roxycarbonyl derivatives and a~ s.logs of benzocycloheptene. Pt.l.
Rocz chemii 37 no .11:1447-1556 '63.

1. Department of Organic Chemistry, University, Lodz.

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Diene synthesis of he%erocyclic rings.

p. 616.

WZADO~IOSCI CHD~ICZNE.

(Polskie Towarzys%wo Chemiczne)
Wroclaw, Poland.
Vol. 9, no. 12, Dec. 1955.

Monthly List of East European Accessions (EM&I) LC, Vol. 9, no. 2, Feb. 1960

Unel.

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, w, F_.

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;:

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.............. . .......................

COUNTRY : P oian,'l h-25'
ABS. JOUR. ' 2~Z,..a JJn.
AUTHOR ;
iN3T. : Lo~z Scientl~'ie
TIT'S] : Foam-Forming ~operties of theo_~c'~'~ of'kryl-
Succinic Acids.
ORIG, FUB, : Soc. scient, lodz. acta chlm.~ 19~8~ 3~ 9-20
ABSTRACT : The possibility Was investigated of utilizing
as ,.~,~B,.n~ the ~roducts of the reaction
acenaphuLene ~ and tet~ahydronaphthaiene
add maiefc ~nhydFide~ on the other~ in the presence of
benzoyl peroxide as a catalyst. Foam foIqa.[ng properties
~tnd s~.,.[a~ tension of so!utlons-of the salts of the thus
jsvntheslzed aryl suaainie acids were eompared~ at different
pa vaguest w~tt~ the correspondinB prope~tie~ o.~
~of liquid soaE. and Merzolya~ D. Hes~ts
showed tJ~e possibil!ty of utl!izinB ary]. succinic acids as
~ ~' in
d.t,t.~,rgen~.s textile and leother industry~ in impregnation
t..,~ wood, in ~.lotation Drocesses~ . G, Bo~vech.
AP~OVED~OR REL~E;j ~t~g~.0~l c:w~!,-~Pe~0513R000617~10019-8'
 ..... Cyc ].ohe ~t,. ne.

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AUTHORS:

� TITLE:
PERIODICAL:

P/012/5~/004/03/10/020

Russocki, Uo; Chrz~szczewska~ Ao; Slawi~ski~ To; Hahn, W Eo
Synthesis of 1~ 6~ 8, 2~, 4~ 6~-Hexahydroxyphenylfluorone

Societas Scientiarum Lodziensis Acta Chimica~ 1959, Vol 4.
pp 90 - 93

TEXT~ The scope of the investigation described in this article was
the synthesis of a hitherto not known symmetrical hexahydroxyphenyl~luorone
in which all otto positions~ as regards the central carbon~ are filled
with hydroxy groups� This goal was achieved by condensation of phloroglu.~
cine aldehyde with phloroglucine in a classical way� The condensation
carried out by heating these compounds in 50~/~a]cohol, acidulated wi~h
H2SO~ in the atmosphere o� a~r or carbon dioxide. The output was between
48~6~%o The same product~ but with lower output and purity~ was obtained
by condensation in concentrated sulphuric acid� There are 4 references~
German and ~ English~
ASSOCIATIONs Katedra Chemii Organiczne~ Uniwersytetu ~Sdzkiego (Lodz
versit~r~ Department of Organic Chemistry)
PRESENTED: ~arch 'f4,, ~959
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P/012/~9/004/0~/12/020

AUTHOR:
TITLE:

� ~ ~ minoalcohol~ III. Investigations of the Influence
Synthesis of Amino~_~�"~_~_~..~one Ring ~pon Addition ~eaction
of Substituents in ~neny~"~~
of Formaldehyde~With Omega_Monoarylhydrazones of phenylglyoxal

PERIODICAL: Societas Scientiarum Lodziensis Acta Chimica, 1959, Vol 4,
pp 101 - 115

TEXT: In connection with investigations carried out by the author,
hydroxymethylation reaction of omega_monoarylhydrazones of
concerning the efs. 1, 2, 5), the author obtai~e& several compounds
oxal derivatives (R ..... ~_~.,oval.~ These compounds were n~t
gly a_monoarylohydrazones o~ pne~A~t,,r~ available in Poland. To
of omeg ~. ~t~fic-l~teratu-
yes describea mn chemmoa~
these compounds formaldehyde was added in the presence of an alkaline cata-
lyst and two new types of compounds were obtained: D_derivatives of alpha
� nd B_derivatives of lo5-diphenyl-2, 4s. . -
ar lazo-beta-hydr�x~pr�P~�p~en�~ ~her. the author lists ma~n pr~
� Y lazo)-pentadmone ~, ~ ~r ~_~o ~n ~urse of his experAm
b~s-(ary - - --~ ~=~ es in ~ .... o
of these compounds an~ ...... o
There are 2 tables and 15 references: 5 Polish, 6 German, 3 English and 1
Card 1/2

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~/012/~/004/0~/12/020
Synthesis of Aminoalcohols III. Investigations of the Influence of Substit-
uents in Phenylhydrazone Ring Upon Addition Reaction of Formaldehyde With
Omega-Monoarylhydrazones of Phenylglyoxe/

Italian.

ASSOCIATIONs Katedra Chemii 0r~niozneJ Uniwersytetu ~odzkiego (Lodz Uni.4
versity, DepartmL.nt of Organic Chemistry)

PRESENTED: January 16, 1959 ~/

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2/012/59/004/0]/15/020

AUTHOR:
TITLE~

PERIODICAL:

Hahn, W.E.

Synthesis of Aminoalcohol IV. Reaction Products of Ome6a~Mon-
oarylhydrazones of Glyoxal Derivatives With Formaldehyde and
Amines ~

Societas Scientiarum Lodziensis Acta Chimica, 195~, Vol 4,
pp 117 - 1~0

TEXT: The subject of the investigations was to carry out the addition
reactions between the formaldehyde and primary amines and between the second-
ary mono- and diamines and the series of omega-monophenylhydrazone deriva--
rives of phenyl- and methylglyoxalo Similar investigations were carried
out by other scientists as wel~, but only with secondary monoamineso As the
result of experimental series described in detail in this article~ several
new compounds were obtained; they were derivatives of 2-aryl..4-alkyl-.6-
acyl-2, 3, 4, 5-tetrahydro-1, 2, 4-triazine. These compounds are formed
with a good output and they crystallize easily� They were not described yet
in chemical-scientific literature. There are 2 tables and 12 references~
5 German~ ) English and 4 Polish.

Card 1/2 ~

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?/012/~9/004/0~/1~/020
Synthesis of Aminoalcohols IV. Reaction Products of 0me6a-Monoarylhydra_
zones of Glyoxal Derivatives With Formaldehyde and Amines

ASSOCIATION: Katedra Chemii Organicznej~ Uniwersytetu L6dzkiego (Lodz Uni-
versity, Department of Organic Chemistry)

PRESENTED: January 16~ 1959 j

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C~ the construction 9f benzocycloheptene. Bul Ac Pol chim ? no.5:
279-283 '59. (EEAI 9:9)

1. Zaklad Chemii OrganiczneJ, Uniwersytet ira. A.Mickiewicza,
(Benzocycloheptene)

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HAHN, Witold E,

Rea�%ions be%~een ~/-monoar~lh~drazone deriva%ives of gl~oxal,
formaldehyde, and primary amines. Rocz chemii 33 no.4/5:1245-1247
'59. (EEAI 9:9)

1. Zaklad Chemii OrganiczneJ Uniwersytetu, Lodz
(Aryl groups) (Hydrazones) (Glyoxal)
(Formaldehyde) (Amines)

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Investigation of the addition of formaldehyde and mercaptans to the
~r .monoarylhydrazone derivatives of glyoxal. Rocz chemii 33 no.4/5:
lZ~.9-].2.,~ ,.,s9. (EEAI 9,9)
(Formaldehyde) (Thiols) (Aryl groups)
(Hydraz ones ) ( Glyoxal ) .

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HAHN, Witold E.
Cyanoethylation of aryl hydrazones. Rocz chemii 33 no.6:lSOl-1503(EEAi 9:9)
1. Zaklad Chemii OrganiczneJ Uniwersytetu, Lodz.
(Cyanoethylation) (Hydrazones) (Aryl groups)

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HAHN, Witold E.; MADEJA, Zofia; PIECHOCKI, Tadeusz
Studies on fluorene derivatives. Fluorene-4-aldehyde (4-formal
fluorene). Rocz chemii 33 no.6:150~-1506 '~. (EEAI 9:9)

1. Zaklad Chemll OrganiczneJ Uniwersytetu, Lodz.
(Fluorene) (Formyl group) (Aldehydes)

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=;: :j. !

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Witold Eo; EPSZTA~i, Jan

Utilization of the ~-~lnnich reaction for the synthesis of heteroct~
-, � 2
ellnical sy. stems4~II, Some derivatives of (_2,>,~,~-te~rahydro.,1,-,A,~
triazine-~ - acetic acids. Rocz chemii 3~ nOoA:907-916 ~61.
1o ~tedra Ghemii Or~,antczne.~ UniwersTtet, Lodzo

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CHRZASZCZEWSKA, A.; }DIPE], W.E.; KACZA~'~, J.
Research on the diacyl$1ycerophosphoric acids. Pt.3.
8:29-35 '62.
1. Depaa.~nent of Organic Chemistry, University, Lodz.
A. Chrzaszczewska.

Acta chim

Presented by

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~. ! ':'~ ;~ ';3~ ', I '~ [ ' !~:i~! il~! :II1~t~

HAHN, W.E.

Oyano~.~hylation of h~drazine deriv~tives. Pt.1. Ac~ chum

1. ~r~ent of ~gnn~c Chemistry, University, L~z. Presented by
W. Hahn,

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~_z~W~.~E~; WEGLEWSKI, J.
Synthesis of aminoalcohols. Pt.6. Acta chim 8:45-54 '62.
1. Department of Organic Chemistry, University, Lodz. Presented
by W. E. Hebu.

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HAHN, W.E.; WOJCIECHOWSKI, L.

Reactions of the dimsrcaptomaleic acid derivatives. Pt.1. Acta
chim 8:55-59 '62.
1. Department of Organic Chemistry, University, Lodz, and Institute
of Organic Industry, Section Zgierz. Presented by W.E. Hahn.

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HAHN, W.E.) TOMCZYK, D.

The reactions of 2,3- and ~/~-cycloalkenequinoline derivatives.
Pt.1. Acta chim 8:61-67 '62.

1. Department of Organic Chemistry, University, Lodz. Presented by
WoW~o Hahn.

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'S/081/~2/000/02~/041/120

AUTHOR:
TITLE:

PERIODICAL:

Hahn, Witold E.
The use of the ~iannich reaction for synthesizing hetero-
cyclic systems. I. 2-aryl-6-acyl-.2,},4,5-tetrahydr�-l'2'4-
triazine derivatives
Referativnyy zhurnal. Khimiya, no. 23, 1562, 299-~OO,
abstract 23Zh242 (Roczn. chem.', v. 36, no. 2, 1962, 227-254
[Pol.; summaries in Russ., Eng., and Ger.])
TEXT: Condensation of RCOGH~NNHAr (I) with R'NH2 (II) and CH20 gives
2-R-4-R'-6-R"-2, ~, 4,5-tetrahydro-1,2,4-triazin~s (IIIa-s, where
R" = CH~COi
R" = GH$OO$ (b) R = C6H5, R' = 0255,
(a) R = c6H5, R' - CH~,
(c) R = C6H5, R' - C$H7, R" = CH~CO~ (d) R = C6H5, R' = iso-CsH7,
R" = CH3C0; (e) R = C6H5, R' = C4H9, R" = GH3CO$ (f) R = C6H5, R' = allyl,
~ R' =
R"- CH$CO; (g) R- R' ~ C6H5, R" = CH3CO; (h) R c6H5,
R" = C.H~CO; (j) R = c6H5, R' = 06H5CH2, R" = c6H5C05 (k) R = C6H~,
Card 1~5

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S/081/62/000/023/041/, 20
The use of the ~Iannich reaction... B166/B101
R' = cyclohexyl, R" = C6H5C0; (1) R = R' = 06H5' R" = C6H5c0;
(m) R = C6H4COOH_m, R' = CHi, R" = C6H5C0; (n) R = C6H4COOH_p, R' = CH3,
R" = C6HDCO; (o) ~{ = ~6H5' H' = �-naphthyl, R" = CH3CO; (p) R = C6H5,
I=
R CH2CH2OH, R" = CH~CO: (n~ W = o

-,, 6.4 2-~' ~ ~ ua~, ~,, = CH=CO; (si R = ~ u �~ _ ~ 5. '
'" = CH3C0)' RCOC(=NNHAr)~H_NHR, (I~ ~-'. ~674"v2 p' H' - ,so_C3H?'
course of condensation, ~ - ~ ~ zormec zn~ermediately in ~he
which is oroved by the indeoendent synthesis of
C6HsCOC(=NNHC6Hs)CH2N(CH3)2 (V) ;nd CH3COC(=NNHC6Hs)CH2N(CH3)2 (VI) with
C6HsCH2NH2 and converting ZVj,t into IIIj,t b~ hea~i~g i~ with CH20.
Reac~ing V with insu��icient quanti~y of C6H5CH2NH2 ~ives
CH~COC(=NNHC6Hs)CH2N(CH2C6Hs)CH2C(=NNHC6H3)COCN5 (VII). The action of
C6HsNHC2H5 and CH20 on I (R = CH3, Ar = C6H5) (Ia) leads to the formation of

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' s/08 ~/62/000/0~.~/0,~ ~/~ 20
The use of the Mannich reaction... B166/B101

2-phenylhydrazone of l_ethylphenylaminobutadi-2,3-one (VIII) alone. To a
mixture of 0.02 moles I (R = Ar = C6H5) and 0.044 moles 37% CHyO in 40 ml
alcohol are added 0.022 moles C6HSCH2Nt{2, this is heated ~or '1 hr a~]d after
24 hfs IIIj, C23H21N$O is precipitated, yield 75%, m.p. 95-96�C (from
CH30t{); the hydL'och.~o,'lde has ~he m.t~. 190-192�C (from ~lcohol). - III
obtained in the same way (the following give's the substance, the reaction
time in hfs, the quantity of alcohol in ml, the gross formula, the yield
as a % and the melting point in �C): a, 1, 20, C12H16N~O, 82, 89-90
[iodomethylate, C13H18N$OI, m.p. 208-210�C (fr6m CH~OH); iodoethylate,
C~4H2oNsOI, m.p. 1S$-189�c (from ace~one).]S.b, '1, 20, C13H17N3O, 78, 52-53
(from 70% CH3OH) [iodomethylate, C14H2oN)OI, m.p. ~86-188�c (from acetone)~;
c, 1, 20, C14H19N5O, 75, 79-80.5 (from 80% CHsOH); d, 1, 20, C14H19N3O,
90, 64-65 (from 60% CHyOH) i e (the hydrochloride), 1, 25, C15H21N30'H�l'
7et 150-152 )from benzene)~ f, 1, 25, C14HlvN5O, 65, 43-44 (from'

Card ~/5

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

$/081/62/000/023/041/120
The.use of the ~[annich reaction... B166/B101

50% CHtOH); g, 1.5, 20, C17H17N30, 60, 119-121 (from CH3OH); h, 1, 20,
C17t117N30, 80, 101-103 (from 00% OH3OH); k, 1, 40, C22H25N3O, 70, 101.5-102.5
(from C~OH) i 1, 1, ~O, 022M19N30, 65, 126-128 (from CH30H); m, 1, 160,
C18H17Nt03, 60, 2~1-233 (from alcohol); n, 1.5, 120, �18~17N30~, 65,
2~9-241 (from 80~ CH30OOH); o, 1.5, 50, 021H19N3O, 70, 160-161 (from
acetone); p, 1.5, 25, �13H17N302, 85, 92.5-9).5 (from cyclohexane); q, 3,
100, �17H16N403, 48, 349-15~ (from CH3OH); r, 5, 100, 012H12N403, 35,
150-152 (from OH3OH); s, 5, 100, C14H18N303, 45, 121-122 (from CH3OH). A
mixture of 0.02 moles'ia, 0.025 moles ~7% CH20 and 0.022 moles �6HtNHC2H5
'in 50 ml alcohol is boiled for 5 hfs, then cooled and the prcduct is VIii,
�18H21N30, m.p. 205-206.5�0 (from CH3OH). A mixture of 0.02 moles VI and
0.04 moles 06HtCH2NH2 in 80 ml absolute toluene is boiled for 8 hfs in a
N2 atmosphere, the solvent is removed by vacuum distillation, and ~O ml
C,r~ 4/5 :

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s/os ~/6~/ooo/o 2~/o4 ~/~ ~o
The u,e of bhe ~[annich reaction... B~66/B10~
CN3OH and 2 ml concentrated HC1 ~z'e ~hen added ~o the residue g~ving ZVt
hydrochlortde, 017H19N30.HC1, yield 77~, m.p. 158-160�C (decomposition;
from V in 6inhrS, yield 80%, m.p. ~o~ O'
produced
acetone-alcoholso~O:~).ml tolueneA'mixtureis boiled .O1 moles V ~nd 0.005 moles
O6~sCH2NH2 for ~O. hfs in a N2 ~tmosphere,fr�m the
solvent, is removed by vacuum diatilZ t , H N 0
~PS' m.m. ~7~_,72oc (Store ~6so-- ~.~ ? iyn~,produci,~ VII C}7 55 ~ 2' ~ield
~,~Grochlori~e,
~Zconoi].j7~ A mixture of O.O~ moles Irt
0.}
Na2CO}, O.~ ml CH20 a~d 10 ml CH}OE is he~ed for
R~I hr~= cooled, R"then ~ ml~wa~erm.p.are ~dded, the produe~ is III k:/" C6H5
O6HSOH2, CH3Co,, 74_75Oc (from 70~ C~9OH). A mix:ure of
O.001 moles IVj~ 0.2 S N~2OO} ~nd 0.2 ml }7~ CH20 in 5 ml CHjOH
for 1/2 hr, producin~ I~lj. [Aba~racter~s no~e: Complete ~ransl~ion.Uis he~ed
J
C~rd 5/5

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/{AHI'I, I'Iitold E.; EI;SZTAJN, Jan

~Feriments in hydrorymethylation and hydroxylation of
,3-pyrido)-cycloparaffin. Rocz chemii 36 no.4:777-778
'62.

1. K&tedra Chemii Oz. ganic.~.nej, [$niwersytet, I~dz.

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U~ili~ation[E ~he ttannich reaction for lhe ~yn%heei~ of
heterocycltd~systems. Pt.i. Rocz chemi/ 36 no.11:1615-i65~

1. Katedra Chemii Organicznej~ Uniwersytet~ ~odz.

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New method for the synthesis of 5~6~%8-tetrah2~roquino]f~eo
Rocm c~emii 37 mool:lC~!12 '63.

1. Department of O~ganic Chemist~y~ Universitye L~dzo

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HAHN~ Witold~ E.$ EPSZTAJN, Jan

Cycloparaffins condensed with heterocyclic rings. ?ts. 1-2.
Rocz chemii 37 no,~:395-~L12 '63.

1. Katedra Chemii Organicznejs Uniwersytets Lode.

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"APPROVED FOR RELEASE: 09/17/2001
! ! ~' . ~' '!~--'~!;~.'~ , i ' ! ' '. '~ I~ I~.:!-'-!ji~-

CTA-RDP86-00513R000617810019-8

IL~HN, ~'[itold E.; bIADEjA-KOTKO'dSKA, Zofia

Studies on products of reduction of some hydroxycarbonyl derivatives
~C l~2-benzo-/k ' -cycloheptene. Rocz chemii 37 no. 7/8:915-917
'63.

1. Department of Organic Chemistry, University, Lodz.

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"APPROVED FOR RELEASE: 09/17/2001 CTA-RDP86-00513R000617810019-8

L 07003-67 ET,'"P (j~! ~',',
ACC NR; APTO01Oi5 (N) SOURCE CODE: P0/0099/66/040/001/0149/0152

~U~I,OR; Hahn, Wltold E.; Epsztajn, Jan; Olpjn_~czaks Bogdan~and Stasiakt

eRG: ~par~enC of Organic ~emist~ University (~tedra ~emil OrEaniczneJ
~iwersyce~) ~

TI~E: S~thesls and ~act~o~ of 2,6-d~al~lpyrld~ne ~analogues

SOURCE: ~czntk~ chemli-a~ales soc~etatls ch~m~cae
1966, 149-152

~PIC ~: hero,cyclic base compo~d~ p~dlne, chemlcal synthes~s, chemlcal
reaction

ABSTRACT: Continuation of work on the synthesis and properties of N-heterocycll�
compounds condensed in tho ortho position with cycloparaffins is reported. Of par-
ctcular interest wore compounds havin~ an alicyclic rir~ conder~ed in the 2 and 3
positions, and an alkyl ~n posttlon 6 in pyrld~ne. Systom~ havin~ L-~o alicyclic
rin&s condensed in positions 2, 3 and 5,6 w~th pyridlno wore also investigated.
Orig. arc. has: 2 tables. ~P~: 35~397./

SUB CODE: 07 / SUBM DATE: 09S0p65 / ORIG REF: OOI / SOY REFI OO1 / 07ri REF~ 004

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 "APPROVED FOR RELEASE: 0911712001 CTA-RDP86-00513R000617810019-8
~. ~ ~'~.,~-'~-~??-~!,! ! ? - I i I:'!!

ACC ~, ,~P~O~Z~-~ ............. i/i) ....... ~,~m&--cO~-.' .... i~)~/~/Oz~o/OO~/OZ, ll/OZ,~o

AU~OR: Ha~, Witold E.; Sokol~sh, A~cJa

ORG: Dep~tme~ of ~g~ic Che~st~, U~versity, ~dz (Katedra Che~i ~g~IczneJ
Uniwers~etu)
TIT~: S~thesis of ~noalcohols.'~ VIII. Derivatives of beta~ercapto-alpha-
arylh~razono-prop~e

SO,CE: Roczni~ che~i-~ales societatis ch~cae polonor~, v. ~O, no. 3, 1966,
4ll-~O
t
TOPIC TAGS: org~ic s~thetic process, s~one, sulphi~c acid, mercapt~, condensatign

reaction, formaldehyde
IABSTRACT: $-Arylhydrazone-~-ketosulphides or sulphones have been obtained in the

formaldehyde, CH and SH acidic compounds yielded the same compounds. The sulphides
were oxidized to sulphcxides and sulphones. Orig. art. has: 6 figures and 2 tables.
EBased on authorst Eng. abst.] [JPRS: 36,OO21
SUB CODE: 07 / SUBM DATE: 20Apr65 /ORIG REF: 003 / OTH REF: 016

i Card 1/1 a~'

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"Movement for S~ving Fmw Materials in Vigogne Spinning Mills.
Magyar Textiltechni]~ [Hungarian Textiles ] Vol.3, ~;o..[2, FP.37E~37~
December 1950.

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HAHIgER, ~Joe

~orkshop experiences with the "Peral~a" rolls. Magy ~extil 13 no.2:
77-79 F '61.

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MAYER, Karel; HAICL, Zdenek

Congenital spinal abnormalities and their clinical significance�
Cesko pedlar. 17 noo5/6:514-517 Je '62�

1. Katedra detsk� chirurgie a ortopedie fakulty detskeho lekarstvi
University Karlovy v Praze, vedouci prof. MUDro Oo Hnevkovskyo

(SPINE abnorm)

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HAiCOV, K. H,

0

I

0 ~

0

0

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"APPROVED FOR RELEASE: 09/1.7/2001. CTA-RDP86-0051.3R00061.781.001.9-8
- ~ '.';~ !; -i~",!l!'i ~! : ~ ~ ~l~l~i;~lt; UE~)~IHiII~!li!~I~II~"T~L~;L~-ti:.":,'":UF;~;i~T'.~F'~I':r~'_~.~'~'~'''~''" .....

APPROVED FOR RELEASE: 09/1.7/2001.

CIA-RDP86-00513R000617810019-8"

"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

"Mechani~a%ion of %he Pressiz~ Process in %he Produc%ion of V Bel%s." p. 1~9,
(~G}{~NI~AGE, Vol. 2, No. &, Ap~. !9~3, Praha, Gzechoslovakia)
SO: Mon%hl~ Lis% of E~s% Europ.an Accesaions, (E[~kL), LG, Vol. ~
No. ~s Va� 19~, Uncl.

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HAIDE, Rudol~
The railroad shunting engine of the No. lO0 type�
14 noo6:187-189 Je '60.
1o Termenyer~ke~iteei es Raktaroza~i Vallalato

Elelm ipar

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LOSONCZY, Gyorgy, dr.s PETRAS~ Gyozo~ dr.; HAZDECKERs Julia,dr.

Diagnostic and eptdemiological data on Klebsiella infections.
Orr. hetil 105 no.lO~,.%~'~,;~ lO Mr'6A.

1. F0Varosi Amszl~ K~rham.

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Electrnlytic production of nickel. ' "'c
Bdn3.-d.r:, Kol~z. Lepol� 83,'o
~,n wa.s me~(c~ m IO'aphite crucibles, rolled into .~hects' :~t :
~,,~, =nt. emo. eney and the quality of the derms/t,.a

' '- . � ~.ung them, pmarl~.qtiOll ~J NJ at
room temp., which I.,ads to reactions of higher potentials
such ,as development of II and O, Best resulLs t~cre
,'ained at t~0�. Th.- material transPort in all eleetrgly:c$

pi! should b,: C~ahlisl~l empirically, When ~roce.~siug
a ca~Ol~e eta pH t~ i:4 t~ Inw lh~ Ni d~p~it �o.tained
NfO in the finm of bilk dot~ antl the ~h~e karl babbles
m~ thc s~fitm. The structure of the dcp~itcd:Ni'lay~
ss~'fin~ with a sulfabi lhaa with a ehloiide ~i~olyte.
~etl c~t ~ud~ w~e ~l~ ~ place of r0 l~ ~oit~. $oln.
t~k pl~ ~Ore rmdilv. ~[etallie con~mNatiol]s of the
an~e exccp{ (~o'dJd n0{ deposit ~ {be eglll~e wil[I c~rlni,

~ hydro.do Co ~'~ea p td b ~ddn of N
.~d N~CI~ ami ~e Cg{OH): ppt. ~ Jemov~ h7 filtra-
tion. ~nrth~ prac~ssihff w~ ~quited t6 sep.'pr~:icm~
metals chie~:. Pt

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

SZUCS, Miklos, dr.; HAIDEgGE~.~Erno; SZEBENYI, Imre

Experiment in coking asphaltic crude oil residues with high
sulphur content. Koh lap 9 no. 10:462-466 0 '54.

1. Budapesti Muzzaki Egyetem Kemiai Technologiai Tanszek.

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HUNGARY / Ohomical Technology, P~oco~'3sing of Solid Fuels

H-22

Aba Jour

,'~uthor
Inst
Title

RZh~(him., No 12, lg38, Nc, 4091~

l(h~ydegger'~ ~gd~3 ~
Not given
Improvemon~ of ~he Yiol~ and tho Quality of tho Products
in tho Coke-Gus Industry,

Ori~ Pub : Negyar Kemik. lepjc, 1955, 10, No 8, 2k4-2~9

~bstract : Eighteen library references.

Cerd 1/1

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-

C1'A-RDP86-00513R000617810019-8

�., ~3, .)~rhmmtalde~ulphud~aUanafdomer. t/c. btt.ralm~us~
i ' c�ah'lotthe~,ducfl�rs�[fmnacec�ke-E-
;~' ~' PP* ~0-~3,~/i&~.) ' ' ; '

~men~l ~'~k xv~ u~deztak~, in
rcdu~ the sulphur ~ntent of dom~llc bltumlnous~c~h:

;...~ nous ~ and' co~ u~ ~ stav~,t~ m~ter;

', anu alternatively la a ~t~m n~ ~i~--'
L. . h)~mt~ and ,team..tu~ted g. were
7 . ammon~. ~e b/ficie~cy of the desulphufi~tlon m:~ ~ �

. ~a 8~s vomme. ~e ~h~ve smmm~ of alii/esot; .
... ~u[ denva~i~ �~ntain~ In ?~ ce~ (a,g sulphiilm,:
~,: - ~pnat~, pyr.es anu o~nic smpnur co unds
[ det~min~ cluing ~e desulphudzafioa ~..
:... ? ~ ~nd.that org~c ~Ur' s~ mm~ e~il' ye' ~'~
~ . ~tfon ~-o~ '~eo '~-" ' ~'""" "
. . . ' hsgh~t'.v~uo'o~ ~IF~r elimina~ by: fl{o ~ms ; ' :
~. ' amoduted to 33,3 ~ for c~/s and 33-6~ for c~; ' :

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8
' " ~ ' ~ ': !; ' '1

T?.e pro~lems of power economy in our century, p. 329. Vol. % ~'~o. 9 Sept.
~.~GY EzN~ERGIAGAZDASAG. Budapest, Hungary.

SDb~CE: East European List, (~YL) Library of Congress Voi. 6, }:o. 1
January

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"APPROVED FOR RELEASE: 09/17/2001 CTA-RDP86-00513R000617810019-8
: ' ' i ' ! ~ I; !~ : ilt'~ ~:~l~t~l.~;~

H~JDEGGER, E.

Significance of iron coke in fer~'ous metallurgy, p. 93.
KOHASZATI LAPOK. (Magyar Banyasz&ti es Kohaszati E~yesulet) Budapest.
Vol 11, no. 3, Mar 1956.

SOUHCE: EEAL, Vol 5, no. 7, July 1956.

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Information on s~nthetic coke. p.90. (Kohaszati Lapok. Budapest. Vol. 11, no ~:, Ant. 1956,
Ontode, Vol. 7, no. ;~.) '

SO: kcnthly list of E~st European ;~ccessions (EE;.L) lC., Vol. 6, ne. 7, julT; 1~57 i'nc]..

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Electroslatic preparation of coal. p.53A. BI~YASZAI'I LAPOK.
Budapest. Vol. ll, no. 9, Sept. 1956.

SOURCE: East European Accessions List (EEAL), Library o� Congress
Vol. 4, No. 12, December 195~

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Hungary/6~nemlcal Technology.

Abst Journal:

Author:
Ins titut ion:

Chemical Products and Their Application -- Treatment
of solid mineral fuels, 1-12

Referat Zhur - Khimiya, No 2, 1957, 5448

Haidegger, Erno

None

Title:

Original
Publication:

Ab s tra.:t:

Card 1/2

The Possibility of Desulfurtzation of Hungarian Brown Coal

Magyar kern. folyoirat, 1956, 62, No 5, 145-148

To study the possibility of lowering the S content of Hungarian high-
sulfur brown coal and the production of sulfur free coke~ an experi-
mental investigation was made of the effect of mineral components on
the formation of S-compounds during carbonization of the coal~ for
which purpose two samples of the coal were treated with 20% solution
of HC1 and coked at different temperatures. It is shown that removal
of the compounds of Fe and Ca decreases the sulfur content of the coke.
Thus~ for example; if the coke of a given variety of coal contained
,3.2% S~ after this coal had been treated with acid the sulfur content

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Abst Journal:
Abstract:

Hungary/Chemical Technology. Chemical Products and ~neir ApPlication __ Treatment

of solid mineral fuels, 1-12
2eferat Zh~r _ Khlmlya, No 2, 1957, 5448

of the coke was
~Ca%ot~u~io~n3%~f--Fem~c~rime_nts in which the cOal was
first
moistened
to coking, have shown that increase ~n ~h~and CaC.l~ and then subjected
pounds Present in the coal increases .... the sulfure amountcontentOf Fe ofandtheCa coke.C�m-
The conclusion is reached that hy means of an acid treatment of the
coal it is possible to lower the sulfur content of the coke produced
therefr~.

C~d2~

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~.Iewer date on the d~stJlletfon cf a coal-oil ~ixtuz. e.

210 (~gya~ KamJkusek I.~pj~. Ye!. 12, no. 7/~ July/Au.,. l~;~'?, BUd~pest~ ~[ur~r,m~3)

~l{'nthl3Febr:.,~IndeXl,.~Scr oJ' 2'sst. Eurooeon. AccessSons (~i::~I) LC. Vol. 7j nr. 2j

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"APPROVED FOR RELEASE: 09/17/2001

.'~3 JOUR. : ,~/.,,n~,~., ~'o, ~]. 193.}, .':'o,

� .,,.,.,, . .~

!/2

CIA-RDP86-00513R000617810019-8

;';:~: ,;.[v,:n - ', , , and

itYdrog~nafi.>n Alcohols oy :~'.~ ,

Magyar Kern La~Ja, 13, No .5-~. 17-180 (1958)

ca~'rieri cut in a ~aoora~ory reactor of 2-liter
ce:Pacify, It has .~ -
" ~en !oun~ tha~ in the :empera-
'~r'e rang~ ~00_330~ ~he optimum., .
Peara 300�' '-e-~Perer. ure ap-
,:~0~,-262 a~m ?ari,'J. nK the pressure in the range
?atLa:~acto~..haa r,o ef/'ec~ on the
Y~eirl:~ uf elcoho/e ~'ere uckie

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"APPROVED FOR RELEASE: 09/1.7/2001.

CIA-RDP86-00513R000617810019-8

1 q c' q I:'0.

76351

~.ithorCatal,.va~ concentratiail~; (oxictea of Cu,
t?)) ore':- ':' ~t" ,~'
-, . ~' ~'- ~ne ,:, ~t ' -.

a ~lxtare of K~ and ~ (739J i~) at a Pre,sure of
315 alto and with 1.5-, wt % catalysn, have shown
withthat the min~um~paceFe~issible temperature .lucrea6e8
increaa~t'g velocity or t~,e reacL:ion
masa~. " ..

~ 'dkovich

273 '

CIA-RDP86-00513R0006171
7983~

.~H~idigger,. E. and Neap, V.
Hungarian Academy of Sciences
Investigation of the Composition of Bitumens and
Asphalts

Acta Chim head S�! Hung, 13, No 4, 525-337 (1958)

]-/2

The results from an investiEatio~n and calculations
made Dy the authors on and for hard and soft bi-
tumene as well as for coal gar product,~ by the
Krevelen method are given; the K:'evelen method
~as developed for the analysis of coal,~ and is
based on the determination of the sp gr and the
elementary composition, it is sho.n that a direc[
relationship exists between the molecular weight
and the structure of the bitumens: the higher
the molecular weight, the greater the n~mber of C

241

10019-8"

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C1'A-RDP86-00513R000617810019-8

?r~,nortion~ o.f ~'as snd electric-~ower ~roduc~zon~' ~nd ~,~ ::i3ni~icance for the
pe:.:er economy of' ,qun~az-yo F.29

~.'bnthly List c.� East Europesn Accessions
Uncl.

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

{L ." H,' I

HAIDFfIO ER, E.;

Pr~uction of f~tty oleoho~ ~ means of high-pressure catal~lc hydro!~enatlon.
P.~

ACTA CHIMICA. Budapest, Hungary. Vol. 19, no. 1, 1959

Ymnthly List of East Europe~ Accessions (E..~3%I), LC. VOl. 8, No. 9, Septm~ber 1959
Uncl.

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"APPROVED FOR RELEASE: 09/:1.7/200:1. CTA-RDP86-00513R000617810019-8

KARCLYI~ Jozsef (Budapest XI, Gellert Let 3); HAIDEGGER,.._.Er]~p (Budapest XI,
Galiert ter 3); HODOSSY~ k%jos (Budapest XI, Gallert ter 3)

Production of fatty alcohols by means of high-pressure catalytic
hydrogenation. II. Acta chimica Hung 24 no.2:157-189 '60.

1. High Pressure Research Institute, Budapest.
(Alcohols) (Ca%alysts) (Hydrogenation) (Copper)
(Zinc) (Glycerides) (Paraffins) (~nganese oxides)

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"APPROVED FOR RELEASE: 09/17/2001 CTA-RDP86-00513R000617810019-8
: - . .:~, ~ , ? ~ , ~ ~,.,17~. '~ IIf~lll~,~

HAIDDGGER, Erno

Industrial ~Fn~�~eanee e� %~e uee ~� so~bt%e.
351-35~. A~ '61

1. Na.~ynyoma~u K~serle~i In~eze%.

Nag~' ke~ lay 16 nc. 8:

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"APPROVED FOR RELEASE: 09/1.7/2001. C1'A-RDP86-0051.3R00061.781.001.9-8

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:~it!'o',a; o::i;!e Pz'~d:;ction ... ,~.., , / ....

7 .
z~k (Ci:ei=~ical l'eclmolo.,;y .,'c;)iu'~l.:,jilL o~ ~:m .~ud{l,)c;{ - �
s~aPtcd in ,iu;:ju:~t !DJ0 on thc injtI'uctio.;s

.:,~.v. i'nd,:atPv). ~'ne !)!ant dcsihulcd
:,J.t~c J.%SC!i' :~l'~d'_:ccd 7 ~Oi,:i Of ilJL,'OLi:~ O/:jj,: i~.' [.!P , :.[ o[' j.'....[. .x'~:--

~'":":: ~,' O5 :-C',!iC~:i .~C~nC~.:;) ii;id the
' I ~ k 13i~-- -' '

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

Card 3/3

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"APPROVED FOR RELEASE: 09/17/2001 CTA-RDP86-00513R000617810019-8

HAIDEGGER~ Erno; HODOSSM, La3os; KAROL~I Jozsef; METZI~G, Jozsef

Realization of �attyaleohol manufacture in Hungary. Magy
kem lap l? no.6:247-252 Je '62.

1. Nagynyomasu Kiserleti Intezet (for Haidegger and Karolyi).
2. 2eti Nltrogenmuwek (for Hodossy and Metzing).

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8
~ : ', ' '.' ;', '- :1".

Dealkylation of alkyl aromatic compounds. Magy kern lap 18
no.11:517-523 N '63.

1. Chemokomplex Kulkereskedelmi Vallalat (for }Iaidegger).
2. Nagynyomasu Kiserlett Intezet (for Kriza).

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Furfuryl alcohol: a new Hungarian chemical product.
Magy kern lap 19 no. 4:196-199 Ap '64.

1. Department o� ChemiCal Processes, Veszprem University
of the Chemi6alC'Industry (for Hodossy).
2. Ministry of th'e Heavy Industry (for Haidegger).

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

L 36~00-66 Z~p(j)
ACC NR, . (D ~OU~CZ COOS:
A~,o~, ~, 3~~ s., ~o~io~l,

0RG: Department of. Inorganic Chemistry, University, I~d~ (Kabedra Chemii Organicznoj
Uniwersytetu)

TITLE: Use of t~e ~M~niah reaction in. ~fnthosts of h.et.e~,oev, '.
Derivatives and analo-,es ^~ ~ ..... ;~,

Roczniki

TOPIC TAGS~ heterocycl~c base compound, amide0 formmldeh2do, hydrolysis,
che~Lc~L reaction

ABSTRACT: 4' 6'diearbometh~xy-1,2 -be nzo ~yclohepbe m.l.dione_
foz'ma~de~e

de~n-~tom~

~rk w~ ~ ~ ~ Cen~al P~ceutie~ ~uat~ '~o~a,,. Orig. ~, has:
S~Card~DCODE: .~ / ~4~ 09Fe~5 / ORIG~F: 002 / OTH~F: 005

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Encased installations with a high voltage, p. 282 The 1957 Electrotechnical
General Assembly. p. 285 Vol. 49, No. 9 Sept. 1956 ELEKROTECHIKA.
Budapest, Pkmg~ ry.

SOURCE: East European List, (EEAL) Library of Congress Vol. 6; No. 1
Jmuuary 1956.

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"APPROVED FOR RELEASE: 09/17/2001
: ~' ~ I~':

C1'A-RDP86-00513R000617810019-8

Interrupter-disconnecting switches of the MS and MSB type. p. 56.

VILLAMOSSAG. (Magyar Elektrotechnikai Egyesulet) Budapest, Hungary.
~ol. ?, no. 1/2, 1959.

Monthly list of East European. Accessions (EEAI).

Uncl.

~c. Voz. s, no.

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"APPROVED FOR RELEASE: 09/17/2001 CTA-RDP86-00513R000617810019-8

HAIDEKKER, Ivan, okleveles~peszmernok

Up-to-dabe bearing supports of propeller
gep ll no.ll:~31-&3? N '6A.

Jarmu mezo

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KORANYI, Gyorgy, Dr.; HAI~, Jud~t, Ih..

~in sensitivity ~o insulin. Orv. he,il. 99 no.8-9:293 23 l%b - 2 Mar %8.

1. Az Orvos~ovabbkepzo In~eze~ (mb. i~azga~o: Barsony Jeno dr. )
Gyermekosz~alyanak (�oorvos: s~einer Bela dr. ) kozlemenye.
(DERMATITL~ K~DICAM~T0~A, in inf. & child
insulin induced (Hun))
(I~ULIN, inj. eff.
clerma~i~ie in child

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C1'A-RDP86-00513R000617810019-8

STEI~R, Bela~ dr.; PUTNOKY, Gyula, dr.; KOVACS, Klara, dr.; SZABONs J~zsef,
dr.; HAIDEKKER, Judit, dr.

~Rxamination of subglottic bacterial flora in a closed system.
Orv.hetil. 105 no.1:21-25 5 J '64.

1. 0rvostovabbkepz~ Intezet, Gyermekosztaly, Laboratoriumi vizs-
galatok Tanszeke, 0rr-FU1-Gege Tanszek.

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� ~TEINER, B.; FUTNOKY, G,; KOVACS, Clara; SZABO,% J,,~ _~..~II_DEFdfER, Judith

Bacterial flora of the subg].ottts in samples taken in a closed
system� The significance of potential pathogenso Adtm pae~iat.
acado sci� Hung. 4 noo2~ll9-131 ~63o

1o Department of Paediatrlcs (Director, Prof. Bo Steiner),
Laboratory (Director, Profo Go Put~oky) and Department of Oto-
rhino-laryngology (Director, Prof~ Lo Subjau), Postgraduate
Medical School, Budapest.
(PHARYNX) (RESPIRATORY TRACT INFECTIONS)
(LABMNG0~COH) (BRONCHOSCOPY)
(BACTERIOLOGICAL TEChnICS) (ANTIBIOTICS)
(EQUIPMENT A~D SUPPLIES) (p~NEUMONIA)

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CIA-RDP86-00513R000617810019-8"

 "APPROVED FOR RELEASE: 09/17/2001
If:. ~i.!-t~' '~-~ ~ , ''' ''! '~ '.! '~ ~ ! ~ ~ ~ ' ~'I!~'TI':' ~ll:'~t'~!

C1'A-RDP86-00513R000617810019-8

LOSONCZYD Gyorgy, dr.; EAIDEKKER, Julia, dr.; MILCH, Eedda, dr.

Staphylococcal epidemics in hospitels with cases of scarlatoid,
0rv.hetil. 101 no.51:1818-1821 18 D'60.

1. Fovarosi Laeslo korhaz es as Orszdgos Komegeszsegug Imteset
(SCA m diag)
(STAPHYLOCOCCAL INi~ECTIONS diag)

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L~) DUDAS, P~; 1L~IDEKKF, R~ Juliet; SCHLAF>~;R, Elisabcth

The later fate of children with Staphylococcal pneumonia�
paediat~ acad~ sci. Hung� 2 nOo2:155-157 '61o

]o Laszlo Ilospital for Infectious Diseases, Budapest~
(STAPHYLOCOCCAL INFECTIONS in infancy and childhood)
(PNEUMONIA in inf and child)

Acta

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The Mechanical Laboratory's ~NB 5516-02 phonograph, p. 73, KEP ES
HANGTECHNIKA, (Optikai es Kinotechnikai Tud~anyos Egyesulet)
Budapest, Vol. 2, No. 3, June 19%6

SOURCE: East E~ropean Accessions Ll~t (E~AL) Library of Congress,
Vol. 5, No. 11, November 1956

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"APPROVED FOR RELEASE: 09/17/200! C1'A-RDP86-00513R000617810019-8

[Co~tea,~, J
ANTONESKU~ N [Antoneseu, N.]l~[~aldu:.'.,C.]l
KOSTIA,
L.

Some problems related to the study ~d construction of the Vuia one-
ton industrial boiler. Rev el,eeSrotechn energet 5 no.1:167-178 '60.
' (EEAI 10:4)
(Rumania--Steam boilers)

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

ANTONESCU, N.I COSTEA, L~ HAIDUC, C.
Aspects of the functioning of the one.ton-per-hour Viua I.E. industrial
boiler with liquid fuel. Rev electrotechn energet 5 no.21~83-~1 '60.
o,5)
(Rumania--Steam boilers) (Liquid fuels)

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AUTHORS:

TITLE:

Sl26216;1/000/0151002101 l
1007/1207
Grecov, D., Haiduc, C. and Soci, A.

Determination of coolant optimum-temperature at the inlet into the nuclear power
reactor

PERIODICAL: Referativnyy zhurnal, otdel'nyy vypusk. 42. Silovyy� ustanovki, no. 15, 1962, 14, abstract
42.15.60 (Studii .~i cercet,~ri energ. Acad. aPR, v. II, no. 3, 1961, 455-467 [Rumanian])

TEXT: The dual-cycle system in which the primary coolant ensures heat removal, while the secondary
coolant (water) is intended to carry the thermodynamic cycle of power generation, is widely used in nuclear
power plants. Proceeding from theoretical considerations, the authors study the influence of the temperature
tI of different primary coolants at the inlet into tim nuclear reactor circuit, ou I ho net efficiency of the power
plant As coolants CO2, heliunl, polyphcnil o~ water may be used. A I'ormt, la is suggested los determining
the optimum value of ti. There are 5 figures and 4 references.

[Abstracter's note: Complete translation.]

Card I/I

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I~.! ~J~.~:~: ~:~-:~ ~. ~ ~ ~ , ~, i -- .'."f ~ .;J~-:.it' t I- : i � : :, (!'lI?~Hl' "l!-'~J'~!~!~t~[l~!~.]']!~!"~ll~$i~'~t'll~'"~'' ""~ ~"' ' -: ' '

.......... s/ s 6]/ooo/ooz/oo /Oo i'

AU~HOBS~ Grecov, D., H~
~I~LE~ ~he calculation of the heating temperature o� feeding w~ter
~ouble-circuit s2stems at nucle~ electric po~er stations

p~ODIC~: Refer~ti~ ~u~, ~a~er~e re~o~, no. 2, 1~3, 10,
abstrmct 2.~0.~ (S~6ii ~i ceroetari enemg. Aca~.
v. 11, no. ~, 6~ -637, Roum~; sun~n~'ies
~ench)

..- ~: Fo~l~ ~e ~ven for calculati~ ~e o~imum terra, re to which :
feed water in d~ble-circuit systems should be heated for ~clemr remc~rs
a therm~ efficiency of 400 Mw. ~e application of the: lo--las pe~itm of
avoidi~ compl~ c~c~ations ~ to find ~e region of the opti~ heati~ t~-
perature with ~fficient accuracy by ~ay of dete~ini~ ~e i~luence of v~ious
factors of the the~l system' on the ~mr~eteP ~ined. ~er~ ~e 2 fi~es
~d 5 references.
[Abstracter' s note: Complete tr~lati�n] ~

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HAIDUC, C.

Bucharest, Revue d'Electrotechnique et d'Ener~_ti__~e, !,To 1. S6rie ~
1963, pp 53-70

"Combined Nuclear Power Plants and their Thez~ual Efficiency.',

j~

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Me~hod fo? deterz~%ning ,-~he opt.imum parameters
J.n ~-:ombined At. omit Power Station with water, pre-
e!ectrotech~, energ~t 9 n~.~:~27-438 '6/.

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"APPROVED FOR RELEASE: 09/17/2001 C1'A-RDP86-00513R000617810019-8

Haidu ;~ i.
inorg;,nic cyclic compounds. Note 1[. On the structure o~' he'teropolva�ids. P. 168.
REVISTA DJ CH! liE. (~,~inisterul Industrioi Fe%rolului si Chi~iei si
Asoaiatia Stiintific~ a !n~,inerilof si Technicisni!or din ~{or~ania) Uncuresti~
Monthly ~st ~f East guropem~ Accost;ions (:~PT~I) 5% �ol. '% no. [i~ Aug. 19~9

U;Ic]..

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.~t,r, 1,~o(,1) '"'

(~t~.~.~LI~", Cluj, llomanl,t).
/,-ram'e lg~O, ~--A new 2..dimensional polycyclicstruc-
ture is proposed foe the Ixdymer (SiNs}I,).. ThL~ new struc-

f'St: N'I
(!). This structure seems m�rc Pr')bablc t hah / IN
does not te~cl to form a double l'x,ud with N. and it nor-
really has 4 co6rdinate Imnds. Structure I ~tisfies these
dt~acteristies. This structure aim accounts e~sily fm
thermM decompn, of SiN'..H~ as well as its reacti,, with

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KHAYDU~, Ione] [Haiduc, I. ]

Systema ~c%~-~'-~lclassification of inorganic cyclic compounds. Zhur.-
strukt.khim. 2 no.3;374-382 My-de '61. (MIRA IS:i)

1. Universitet imeni Babesh-Bolyay, g. Kluzh, Rumvnskaya Narodnaya
Respublika. '
(Chemistry, Inorganic--Classification)

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HA]DUGs Ionel

~arborani, ~02Hn%2, a new class of quasi aromatic compounds.
Studii cerc chim 13 no.11:783-803 N '64.

1. Faculty of Chemistry, CluJ University, 11 Arany Janos Street�

~ ?'-il; l'~ I ' ~:,~,,

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