SCIENTIFIC ABSTRACT MOSYUK, M. F. - MOSZEW, J.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001135410016-9
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: July 13, 2001
• Sequence Number: 16
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

M05YUK, M. P.
Fertilizers and Manures
Action of mineral fertilizers in drained peat bogs. Pochvovedenie, Ho. 6, 1952.
Monthly List of Russian Accession , Ubrax7 of Congress, August, 1952. UNCLASSIFIED.

USSR/Cultiva"L-lu('. lllant,- - Grains.
Abs Jour .'u.' '1,,ur - Biol., ND 9, ."9211
Author '~,~)syuk, LN.F., TyurriQsAv-,, G.A'&,
Inst
Title 'f,.c InIluence of Lupiiic o.i t1to Iiicrcasc,
!lye Crops and on Soil FurtU-'.y.
OriZ Pub !~cl-acdaliyc, 1957, v) 6, 4,j-44.
,'Jistract The ,~L-cjvrth of ourtacc aat" 3u,)3urface nasses -is well as
tlicir 11, K alvl H contci-.'~-s was tlctcrxr.,"Jacd in fiel(I Qx-,,~rl-
nonts at the CheraiL;ov aL;r.'Lc,,LItura1 experinent statiI.I.
Dic exTcrimnts were conCuc,;c!(. at various tina's lu-
r
pine is LathereO. ~,~r L;roc:n ~oddar, for ansila.-a, f.D.- 5,~c(ls
and for plowinG in as m,iure. The surface 0;-y lit d-
ne Lrizz L;rows from 36 cw~/aa Ln its blossoriint~ rlmsc up
to 106 mrt/hn when 'ully ripe, anc! tlic subsurface -'ry imss
dininishes from 17 to 14 cA,--./,a. Mic root Greatest ~..ass
Card 1/2
L~5

,,-.XOSYUK, M-F-,kandidat sellskokhozyaystvannykh nauk.
Iffective, help to agrochemical laboratories of machine-tractor
stations. Mauka I ppred. op. v sellkhoz. 7 no.2:43-" 7 '57.
(KLBA 10:3)
(Soils--4nalysis) (fertilizers and manx=es)

KOSMK, M., kand. mallskokhoz7aystvannykh nauk
On what the effectiveness of bacterial fertilizers lepands.
Nauka, i pared. op v sellkhoz 9 no.5:50-53 my 159.
(MIRA 12:8)
1.Zaveduyushchiy agrokhimicheskoy laboratoriyer Chernigovsko7 sel'sko-
khoz7aystvennoy OP7tno7 stantaii.
(Soil inoculation)

POiAbU
M03ZCZYN3FA, Janina, dr inz.
Donartment of Technology of Electronic Devices,
Pclitechnikaj, (Katedra Technologii 3przatu Elek-
tronlesnego Politechniki), Warsaw.
'Narsaw, Chemia analit-yezna, No 3. May-June 1965,
pp 305-309.
"Zero-current notentlometry, Part 2: The determination
of silver*"

WLODARCZYN , Janina; MOS,'c7YNSKA , Danut-a
GeneralJied lymph nodr, tubi~rcu~osis Ioca'izad In '~he
abdominal'cavity. Pol. tyg. lek. 19 11 My 164.
1. Z Katedry Medyc,ny Ogolnej Studium Doksztalcania Lekarzy i z
Oddzialu Wewnetrznego "A" Szpitala Wojewodzkiego we droclawiu
(kierownik: prof. dr. med. Jozef Kaniak).

PIOSZCZINSY,T, Aaeksander
Controlled atmospheres az applied Ta:-rertly Ln heat treat-ment.
Problazy proj hut masz 12 no.41l0l-ll~6 #16-4
1. Instytut Mechaniki P-reay%-yjnej, 'ilarsmava.

AA 2_ 6 /V,S A:
POLASD
!-:A.~CCOWA, Janina and NARZE-11;, Alfred; Soacnd (1*:)
(III) Surgical Cltni6s (XlinLka
mia '..Iodyczna. Modioal Acadomy] In Xraj*uw(Biroctors: Profs.
qE5--L--Q-iZACK1 and J. JASILSSKI, rospootivoly) and the
Special Laboratory (Praoo,.nia SpoejaIna) of the Riclottsia-
Virus Division (Oddzial Riolcottsjowo-Wirusowy), Plant for
the Manufacturo of Sora and Vaccines (WytwvrnIa Suroido I
Szozopionoic) in Kralcow (Dirootori Dr. Z. ~10SZCZr-14SKI)
"Reaction of %hito Mioe to Intramodullary Inoculation with
Encephalitis Virus.$'
learsaw-Krakow, ?rzoirlad Lakarski. Vol 19. Sor 11, No 4. 63,
pp 222-224.
Abstract: [Authors' Russian summary] In the course of In-
vestir,71ting experimentally the reaction of bone tissuo to
various viruses. the authors found that both the S47 str"11
and the equine encephalitis virus of the American Idoz;t are
pathogenic to %ftito mica on intramodullary inoculation. ancl
retained in the bone tissuo even 10 days after inocula-
on in lothal quantities, even though encephalitis has
lady got in. Six Polish and one English references.-
i

GORSKI, Andrzej; ~9~ZITNSKA, Janina
Rapid chromtograpbLic micromethod of determining the total
zirconium and hafnium contents in sulfuric-and oxalic-acid media.
Chas anal 5 no.3:395-400 '60. (EM 10:8)
1. latedra Metaloanavatwa Folitechniki, Warszawa.
(Chromatography) (Zirconium) (flafnium)
(Sulfuric acid) (Oxalic acid)

MOSZCZYNSKA, Urazula
Border strata of the Kat-owice-Weino-diec region. KwartalddlWol
5 no-4:987-988 161.
1. GQr.noslaska Stacja Terenowa, Instytut Geologiczny, Warszawa.

FUSON, Jakub; NUUMSZUGI Stanislaw; KOSZCZYVSKA. Zofia
Rodifications of qualitative content of serum proteins and erythro-
cytes sedimntatiou during trichinoste. Polskis arch. m94.
vownetrz. 23 no-5:683-688 1953,
1. Z II Kliniki Chorob Wevnetranych Akademit "cznej w adansku.
Kierownik: prof. dr wed. J.Penson.
(BLOOD COAGULATION. in various diseases,
*trichinosis)
(BLOOD MIMENTATION. in various diseases.
Otrichinosis)
(TRICHINOSIS, blood in,
*coagulation & sedimentation)

KOMUNSKA-ELLICINSKA, Zofia; XALICIVSKI. Andrzej
Viscosity of the blood in neoplasms in awn and rat and in normal
and fasting rats. Polski tygod. lek. 9 no.24:737-739 14 June 54.
1. Z Instytutu Oukologil w Glivicach, dyrektor: dr med. J.Swiecki,
Zaklad Biologit ftwotworow, kisrownik: prof. dr r.Dux.
(Bww.
viscosity in neoplasms in man & rat & in normal
& fasting rate)
(HROPLASKS, blood In,
viscosity. in man & rat)
(FASTM, effects,
on blood viscosity)

BROSS, Wiktor; AMISKI, Anatoni; KOSZCZYNSKI, Ludwik; ROGAISKI. gugeniusz
Application of ultracortenol in conservative therapy of chronic pul-
monary abscess. Polski przegl. chir. 30 no-5:578-580 Kay 58.
(IMIGG, abscess
ther., prednisolone trinothylacetate (Pol))
(21.GMLSOWNZ. rel. cpda.
prednisolone trimethylacetate, ther. of lung abscess (Pol))

MOSZGZYNSKI, Ludwik; CZEREDA, Tadeusz
Entero-gastric invagination after resection of the stor-Act. Polski
prze#l. chir. 33 no.5:4'71-475 '61.
1. Z Il Klinlki Chiruz,gicznej A.M. we Wroclaviu Kierownik: prof,
dr W. Bross
(EkUSSUSCEPTION etiol) (GASTR ECT-DN Y compi)

BR03:3, Wiktor; WHZLINWICZ, Wladyslaw; MOSUMISKI, Ludwik; MASL4111U, Pawol
Our obsel-vations on the treatment of pleural hezatumas. Pol. tyg.
lek. 17 no.31:121&-1222 30 JI 162.
1. Z II Kliniki Chirurgicznej A14 we Wroclawiu; kicr.: prof. dr
Wiktor Bross.
(PLEURA) (104ATGIA)

POLAND
CZEREDA, Tadeusz, MQ�_&gjYXSK1, Ludwik, and KNAST, Witold;
Second Surgical Cri-nic (II K-1-1-n-iYa-Chirurgictna.), AN [Aka-
demia Modyczna, Medical Academy] In Wroclaw (Directors Prof.
Dr. Wiktor BROSS)
IlDifficulties in Diagnosis in Pyogenic Aftesses."
Warsaw, Polski lxgodnik- Lakarski, Vol 18, No 2), 3 Jun 63,
pp 822-825
Abstracts [Authors' English summary modified] Authors dis-
cuss difficulties in diagnosing liver abcasses (not frequent
since the advent of antibiotics) and the complications they
cause. 7hoy cite an example of four cases with undetected
abeesses sent to surgery, of wbich two proved fatal. 1hey
specify symptoms there special car* should be given to this
diagnosis and recommend the diagnostic procedure. 7here
are 13 references, five (3) oach of Poliah, Soviet, and
English.

BROSS, Wiktor; KOCZOROWSKI, Stefan; BADER, Otton; WREZLEWICZ, Wladyslaw;
BROSS, Tadauez; CZAIVIIECKI, Leon;
Our observations on the treatment of necrotic pancreatitis.
Pol. przegl. chir. 35 no.10/11:1168-1169 '63.
1. Z II Kliniki Chirurgicznej 14 we Wroclawiu Kierownik: p:-of.
dr W. Bross.
(PNICREATITIS) (SURGERY, OPERATIVE)

MOSZCZYNSKI, Stanislaw, mgr inz.
A new simplified method of determining and analyzing power losses In
electric networks. Energetyka Pol 14 no.11:338-341 N 460.
(EUI 10: 3)
(Electric networks)
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g. ld AcPb with I(M.7. a. at (me-64"I.Nif I,LS try looratlag
Sur to bw at ISt-:1W amod at 3101 fm a sburt whilot to
mmvw thor M"*NH, spik out. gave culark-sis meordin ol
Yi-4-(W-tdi*MiSt) I
LIrw
mo 134 6% UCI molt. st. 17"'; pwrok. a
96"'; Ac dooow.. mg.
derow.. as. 144'. The cinsorw ed I with a1r. K011 at jW*
kor 6 bm. andror presommot gave c4finollm rAvdki at 2-pbewo.
C.H~*NO. so. 2011 . Loin-
(n)
Mwk vitch the car I ag imam 7-owthtrklocincoMoor.
em. 2-40' (Bor. V. I3P7(IW4)L Simollarly the ctaclenss-
it= of W g. d PlIctilias "k FAA ff. no (PbNH)NCS at
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"*IrMpAM*wcMw dev*., W. IWA *I
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&W
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POLAND/Organic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Ref. Zhur. Khimiya, No 11, 1956, 3615o.
Author : Mbszewo Inasinski, Malle.
in -Y
st : ot-irven.
Title : Synthesis of New Colamino Esters with Antihistamine Pro-
perties.
Orig Pub: Zscz. nauk. Uniw. Jagiellonskiego. Mat., fiz., chem.,
1955, No 1, 189-2102-
Abstract: Esters with the general formulas o-RQV'H*0CH 1Z CH..,.~HZCH,,NR',*
(I) and n,n'
-RC!&HqS0;C6H4OCH4CH;NRj (II) were synthesized.
On the basis of preliminary data I and II (particularly
when R = CHj) possess strong antihistamine properties.
I may be obtained by mixing a solution of RjNCH~CH;,0Na
(III) in 200cc. of toluene with a solution of o-RC(,HyGCH
CHZBr (IV) in 200ce. of toluene. After boiling for 4
Card 1/3 17

POIAND/Organic Chemistry. Synthetic Organic Chemistry. G-2
Abe Jour: Ref. Zhur. Xhimiya, No 11, 1958, 361.5o.
hours, followed by the addition of a dilute HC1,
neutralization with KOH, I is extracted with ether.
The following characteristics and physical properties
listed represent respectively: R,R', quantities of ~ii
and IV in gr., yield of I in gr., boiling point in C,
melting points of I -HC!l and of I - CHJ in OC. They are:
H, cH,, 9,2o.i,6.2, 145-146/gmm, 101-102, 91-92; H,C
,z H5-,
11.8, 2o - I, lo.4, i65-167/io mm., 8o-81,-, ethyliodide,
melting point 99-1000C; GH30, CH3, , 23.1,6, 176-178/i4mm,
112-113, 131-132p- CH10) C-O II.8.,~b-1,5, i89-i9o/i4mm,
Ni P int 103
115-116,-, Fthyliodide, mil ng 0 -104. A mixture
of III in 8cc of toluene and n, n1RC!,,HqSQ,,C4HyC!1 (V) in
10cc of toluene when boiled for 4 hours followed by the
addition of 20ac of toluene forms a precipitate, which
after filtering, is extmeted with dilute HU. The re-
Card 2/3

POLAND/Organic Chemistry. Synthetic Organic Chemistry. G-2
Abs Jour: Ref. Zhur. Khimiya, No 11, 1958, 36150.
sidue is then decomposed by means of a 101p4 NaOH solution
while heating and thus obtain II. Given below are phy-
sical constants obtained representing respectively: R,R',
quantities of III and V in gr., yield cT II in cfj, 0 melting
points of II, of chlorhydrate, and of picrate in C. They
are: H,H,3,8,2,15,85 (from toluene), 264 (from dioxaline),
233; H, CH3,3,6,3,45,97, 181,40; H,CZHj-,4j,8,5,6O,79jl68
(from dioxaline),162;CH5,H, 3,8,5,26,1-~~9-14o,277,225;CH-3,
CH?.92jP6s6Oj99, 165y-;CH3, C,,Hj-, 4,9,60,61,152 (from clioxa-
line).
Card 3/3

PCLAND/Orgnnic Cheuistry. Synthetic Grganic CheListry- G
Abs Jour: Ref Zhur-Khir..., No 2, 1959, 4682.
Author Moszew, J. and Zai-Jcwska-JaBinskj~, W.
Inst --+- -
Title The Preparation of Eveacyclene.
rrig Pub: Roczniki CheLl, 32, M,L 1, 12c)-130 (1958) (1,,-, Polish with a
GerT--nn Surynry)7
Abstract: 3.36 gLs of acenrphthencne and 2.74 gus 2-NIIjCjHIt
COOH are heated for 24 hrs at 1-10" after which
they are heated for 24 nore hrs at 210"; the rRlt
is refluxed with 30 -.i1 alcoholic KOH, giving a
1% yield of decacyclene, rip 3870 (from xylene).
The alkaline layer yields 2,3-perinaplithylene-4-
hydroxyquinuline, yield Z~, rT., 430: V. Skorcdux.-.ev.
Card 1/1
25

POLAND G
-nther
Organic Clierristr`Y- Sy '~c Organi, ~:hemtjtry'
Pef
Moszew, J,e-Zarikowska-jasinska, W.
On the Structure of 2,3-pari-Naphthylenoquino-
line and Itz Derivatives
,r Roczn. chem., 1958, - -233
~32, No 2, 225
In order to prove the position of substitutes
in derivatIves (I) obtained earlier (Ref T-iin--
i~him, iP55). 28953) by condonsation of' Acenaph-
thenone (II) with 2-NH2C61f4C00H (III), 4-HO-1
(IV) was prepared, and by the condensation of
II with 2-~TH2-4-CH3C03COOH M, 4-1i0-T-CH3-1
(VI) was synthesized; along with 1V and VI,
~ecacyclene (VII) is formed. DuTing attempts
at condensation of II with 2-Cl-3-C"'3C6HXH2
(VIII) or (2-C1-3-C"H3C6H3N'f)CS (IX), Ins-teari
1/6
G - 51

FC G
t
He' Zn-jr 5, 1)59, 1-C408
of the expec-ed derivatives of I, P -inixtur-3 of
icon~ld. VII and biace'none (X) was formed. 3.36 g. of
IT and 2.74 9. of III are heated for 24 hours
2/6

G
Y
'el' char Kr-i-=, 1 45~, lio - [:"40,9
-It T,
0
a- 110 axid then 'or another '4 hoLrs by i-
cont'd. creasing the temperature to 2100, the trit-u-
rated mplt is extracted with alcohol and then
with an alcoholic solution of KOH; from the
al'f-.aline extract of' HC1, 0.~ g. of TV is se-
parRted out, M.P. about 4-10 ; benzoyl derivq-
tive (BD), M.P. ~41 0 . The residue which was
not dissolved in alcoholic KOH solution (0-45
9-) is VII, m-P- 3870 (from xylol). 1.68 g. of
II and 1.51 g. of V are heated for 70 hours at
3/6
G - 52

G

Pef Zbi-

L
1 P~

r 0
of X is obtnined, 260 (from ~~hloroform);
contid. from tho residue of the extrantion, VII 13 se-
parated out. Analogous results are obtained by
the additicn of 0.07 g. of V1II-ZnC1j (two
hours 2000), or 1.3'~ g. 01' COef"C;S -(fO'Jr
'
-'
e same qua
~titics of IT
hours: 2000). From th
and VIII, with the addition of a few drops of
concontratled HC1 (20 minutes, 120'), 0.16 p.
2.5 g. of II and 5 g. -)f IX
of X is obtained.
0
are melted at 0 , heated for seven hours at
5/6
G - 53

m

77=

t bim

tath
r

1960, No.

NO' Vf-r.
LC I Loy Orc -

'I u P. q r, rz tne 6 o a n r

tn~- C"
ion of 5"'
-
2
?

ro -1, -n i tro--' n .3 t
t a I~J cl-atcm in
8 ~,f! e - ef, a I i F n P 11 7 edUC jC) ti t o ~.,-c ri 10 T 0
a,: -; fA r 11 ', t ricl t h c, r -
ver!rion of ill to 2-c,,Ioro-i-ntipnti-ioxiaccti,-
via tne di!3zcn~,im compoki-A. 10 ~-~qs c f
added -radua.ly w-~th cooling to 5 gms n
D

CA I -IT-, Of. y
ABS. JM. RZ"l at N09 5 19600 Wo. 1?825
t
alm. Pn.
tABSTPICT S hot Ci~ ZU,~AJ ana the r83U -,;clut-' 3n is heate
for -jrs a *- a bcfuL I bt a: neo,
w. p!'?~* from -.7", '~0011 ar,(i aquecun a3 met
, I lc
c s (NE) mr, 11 "rom -'P, et ester mp
rom alc ?lm"de ~fr-jm r. e r-, E c fa ii d c., r.
-4 hrs at ajou. mp 2-;70 I-'rom zil-'.
Tms of 11 in 2X 7- - c c n ~-s treated gi-4-lu-
sliy at aoout 100* aith z.-- .7ms Sr, in 100 m' H-1,
tthe omnlet-ior. of tne rc~' ction cne-half VC-Te
of water is addej, ne S~Jlu+iQn -I's nealed tr- ricil-

COUNITPIr Pol nd
s RZKMM., No, 42, 1960., 91),
CR I r" PUB, I
'A 3~~ CT -;n;.,), coolled, Wfli NaOii ~.r, uldeu until. a -,trong a~lk-
a.Line reacti-or, is .rie solxition is nrqtp~'
for I hr, coole--i, and di!;-zolved in aqueois
d"s of -711 are obtaLned, mp_-.-250' (decor-.;
f r- om ail aic ) , '-IS -.ID 11~n' 'from a1c), ethyI eLer
mp 161* ~,from a1c) , air, jAe Tp i35* (from water),
acetyl eierivative mp 2Z 5' (from viater). I! exhib-
it~~ an effpct or plan-' Kroatn; the ef-
f-ct ~-s narkcd in t-e :aEe of trusta-d a,-,d c--nsid-
etab,y weaker in exper.ments with flax.. For rnt-
162

-Mosaw, J.; MIREK, J.
On the synthesis of some isomeric quinol-ineoxyacetic acids. P.365
ROCZNIKI CHMI. (Polska Akadev&a Nauk) Warszawa, Poland., Vol.33, no.2, 1959
Monthly List of East European Accessions (EFAI) LC, VoI.E, No.5,, .3eptenber 1959.
U ncl.

.MPSZEWP J. INASINSKI, A.; KUBICZEK, K.; ZAWMYKRAJ, J.
Addition reactions in the group of Schiff's bases. Addition of iso-
thiocyan acid eaters. 1. Bul chim PAN 8 no.8:405-/.08 160.
(EFAI 10: 9/10)
1. Katedra Chemii Organiczn%j, Uniwersytet Jagiellonski, Krakow;
Pracownia Mr. 6. Instytut Syntezy Organicznej, PAN. Presented by
T. Urbanski.
(Chemical reaction) (Schiff bases) (Thio"anio acid)
(Isomers) (Esters)

MOMWO J.; INASINSKI, A.; BOKSA, J.
Addition reactions in the group of Schiffle bases. Addition of
isothio--yan acid esters. II. Bul chim PAN 8 no.8:409-411 160.
(EEAI 100/10)
1. Katedra Chemii Organicznej, Universytet Jagiellonski, Krakow.
Laboratorium Nr. 6. Instytut Syutezy Organicznej, PAN. Presented
by T. Urbanski.
(Chemical reaction) (Schiff bases) (Thiocyanic acid)
(Isomers) (Esters)

MOSZEW, J.; INASINSKI, A.
Addition reactions in the group of SchlfflB bases. Addition of
isocyan acid esters. III. Bul chim PAN 8 no.8:413~-416 160.
(EFAI 10: 9/10)
1. Katedra Chemii Organicznej, Universytet Jagiellonaki, Krakow.
Laboratorimm Nr. 6. Insty-tut Syntezy Organiamej, PAN. Presented
by T. Urbanaki.
(Chemical reaction) (Schiff bases) (Thiocyanic acid)
(Iaomers) (2sters)

,; BOJARSKI, J.; RIASINSKI, A.
--MWZEW,J
Addition reactions in the group of Schiff's bases. Addition of
aromatic derivatives of carbodlWds. I. Bul chin PAN 8 no.8z
417-418 160. (RUI 10:9/10)
1. Katedra Chemil Organiamej, Universytet Jagiellonski, Krakowi
Iaboratorilum Nr. 6. Instytut Syntezy Organicznej, PAN, Presented
by T. Urbanski.
(Chemical reaction) (Schiff bases) (Aromatic compounds)
(Carbodiiside)

KOSZEW, J.; KOSSOWSKA, H.
Stersocheadcal problem in the erynthesis of sox* 2,4-disubstitmted
chinolins compounds. Bul chim PAN 8 no.8:419-422 160.
(MAI 1019/10)
1. Watedra Chemii Organiesnej, Uniwersytet Jagiellonski, Krakovi
taboratorium Nr. 6. Inatytut Syntezy Organicznej, PAN. Presented by
T. Urbanski.
(Stersochanistry) (Quinol-ine)

G/OG3/b0/O1U/001-4/0G4/C,-G6
B005/Bo6c)
AUTHOR: Moszew, Jan (Krakow)
TITLE: State and Prospects of
People's Republic
n the Polish
Organic Chemistry i -
PERIODICAL: Journal fUr pra-ktische Chemie7 19bO, Vol. 10, No~ 1 4,
pp. 90 - 101
TEXT! The present paper is a reproduction of a lecture which the author
delivered on the occasion of the 550th anniversary of Leipzig University.
In Poland, investigations in the field of theoretical and syntnetical
organic chemistry have been made especially at universities and partly also
at the medical academies; furthermore, at higher schools of agriculture and
economics, and at the Institute of Organic Synthesis of the Polish Academy
of-Sciences. The studies on the alkaloids of Peruvk an bark and lycopodium.,
on tEee--"s'--t-ereochemistry1of polycYclic hydrocarbons,lon new methods of
synthesis and conversions of jj~ ~oa~affinsland quinol in compounds on
apparatus and methods in elementary analysis are worth noting. The main
part of this paper deals with a survey of the successes achieved in the
Card 1/3

State and Prospects of Organic Chemistry G/003/60/010/ Col - 4/0U4/006
in the Polish Peoplels Republic B005/BO6O
above-mentioned fields of chemical research and of the plans to be -arried
out in organic chemistry in Poland. Studies of the rates and mechanisms of
many chemical reactions were made at Warsaw Technical. University At pre
sent, extensive stereochemical studies are being made on polycyclic hydro~
carbons, especially naphtha3ene derivatives, under the supervision of
Professor J, Susz 'ko at Poznali Universi~y. The successes hltheTlo act._,eved
are mentioned. In the field of the alkaloids of Peruvian bark, special
attention has been devoted to the possibility of synthesizing higher etLer
homologs of epi-alkaloids of the quinine group. Professor T, Urban'ski of
the Warsaw Technical University studied the preparation an,~"r_e'a`-ct__i`on__s_ -of
nitroparaffj-ns which are of special significance as intermediate products
in the synthesis of important commercial compounds. The most important
results of these investigations are given. Extensive studies of the
chemistry and reaction mechanisms of mesoxalic acid dinitrile are also tc be
mentioned. The most important results obtained in the chemistry of organic
phosphorus compounds are also given. In the field of heterocyclic compounds,
the synthesis of qu1noline compounds and terpenes was especially stualed.
In recent times., investigations on organic contact processes nave been made
a', Narsaw Technical University Polisr, physiral chemists succeeded in

State and Prospects of Organic Chemistry G/003/60/01C/00, 4/(D(j4~/oCi8
in the Polish People's Republic B005/BObO
developing new methods, above all in the field of potentiometric f-,iroma*,,--
graphy. Professor B. Bobranski improved semimicroapparatus for the
elementary analysis of organic substances, The author notes that ttie
general results obtained in organic chemistry in Poland are lnsuffi~ient.
The following Polish scientists are mentioned: B~ Bochwic, J, Ricnalski,
H~ Kuczy~ski, E. Sucharda, S, Malinowski, B. Kamre~nski- IN. K-e-mula.
ASSOCIATIONz Krakau, Universit6t (Krako"w University)
SUBMITTED~. September 16 1959.
Card 3/3

MOSZEW, Jan; INASINSKI, Antoni; KUBICZEK, Karol; ZAWRZYKAJ, Jerzy
Addition reactions in Schiff's bases. I. Addition of the esters of
isothiocyanic acid. Rocz chemii 34 no.3/4:1169-1172 '60. (EEAI -10:3)
1. Katedra Chemii Organicznej Uniwersytetu Jagiellonskiego,
Krakow i Pracownia Nr 6 Zakladu Zyntezy Organicznej Polskiej
Akademii Nauk, Krakow.
(Esters) (Isothiocyanic acid) (Schiff bases)

PASINSH, Antoni
Addition reactions in SchiffIs bases. II. Addition of esters Of
isocyanic acid. Rocz chemil 34 no-3/4.1173-1176 160. (EMI 10:3)
1. Katedra Chexii Organicznej Uniwersytetu Jagiellonskiego, Krakow
i Pracownia Nr 6 Zakladu Syntezy Organicznej Polskiej Akademii Nauk,
Krakow.
(Eaters) (Isocyanic acid) (Schiff bases)

X - INASINSKI. Antoni
-- QSZW, Jan: BOJARSKI. Jacek,
Addition reactions in Schiff's bases. III. Addition of aromatic
derivatives of carbodiiaide. Rocz chexii 34 no.3/4sll77-1179 160.
(EW 10:3)
1. Katedra Chemii Organicznej Uniwersytetu Jagiellonakiego,
Krakow i Pracownia nr. 6 Zakladu Syntezy Organicznej Polskiej
Akadexii Nauk, Krakow.
(Carbodiiaide) (Aromatic compounds) (Schiff bases)

MOSZEW Jan- WACHALEWSKI, Tadeuss
-,- X_
Benzyl derivatives of 1-naphthylacetic acid as plant growth regu-
lators. Rom chenii 34 no.5:1387-1396 160. (SW 10:9)
1. Katedra Ghemii Organiesnej Uhiwer"tu Jagiellonskiego, Krakow
i Pracownia Nr. 6 Zakladu Syntezy Organicznej Polskiej Akademii
Hauk, Krakow.
(Benzyl group) (Napthaloneacetic acid)
(Plants) (Growth(Plants))

MOSZEW, ~!pj _4AWEtZYKRAJ, Jerzy
New sulfonic compounds of naphthalene series. Rocz chsaii 34 no.5:
1465-1469 '60. (EFAI 10:9)
1. Katedra Chemii Organicznej Uniwersytetu Jagiellonakiego, Krakow.
(Naphthalene) (Sulfonic group)

MOSZEWI J.; KOSSOWSKA, H.
StereaebeMedl -in tQWsynthegig of-jow 2,4-disubstitutp-d
quinoline compounds. II. Bul chim PAN 9 no.4.217-218 161.
1. Katedra, Chemii Organicznej, Uniwersytet Jagiellonski, Krakow
Pracownia Nr. 6. Zaklad Synthezy Organicznej PAN. Presented by
T. Urbanski.
(Stereochemistr7) (Quinoline compounds)

MOSZEWV J.; SULKO, St.; SLEDZIEWSKA, S.
On a variant of the synthesis of quinolino-quinoline eompcnmda. Bul
chim PAN 9 no.4:219-223 '61.
1. Katedra Chemil Organicanej, Univer"t Jagiellonski, Krakow
Pracownia Nr. 6 Zaklad Syttezy Organicznej, PAN. Presented by T.
Urbanski.
(Quinolinium compounds) (Quinoline)

MOSZEWV J.; SULKO, St.; SLEDZIEWSKA, E.
Influence of some substitnents in the position 2,4 and 6 of the
quinoline ring upon the absorption capacity in the ultraviolet.
Bul chim PAN 9 no.4:231-236 161.
1. Katedra Chemii Organicznej, UniwerBytet Jagiellonski, Krakow
Pracownia Nr. 6. Zaklad Syntezy Organiesnej, PAN. Presented by
T. Urbanski.
(Ultraviolet) (Quinoline)

MOSZEWV J.;-PIASINSKI, A.
On the transformation of anilide derivatives of arowtic /0 -keto
acids. Bul chim PAN 9 no.53303-305 161.
1. latedra Chemil Organicznej, Universytet Jagi&Uonski, Krakow.
Pracovnia Nr. 6 Zaklad Syntezy Organicznej, PAN. Presented by
T. Urbanski.
(Anilides) (Aromatic compounds) (Ketones) (Acids)

MOSZEWI J.; KUSMIERCZYK, St.
The transformtions of anilides of the aliphatic (Y- keto acids.
Bul chin PAN 9 no.5:307-308 161.
1. Fatedra Chexii Organiamej, Univer"t -Tagiellonaki, Krakow.
Pracovnia Nr. 6. Zaklad Syntesy Organicznej, PAN. Presented by
T. Urbanski.
(Anilides) (Ketones) (Acids)

SLFD/,I,;WSKA, Ewa

1, qr",P! floge r. u'4
I . ar tne n t n 'Fig
K r ak r-. w . 3u but i f, '.,i f - r

i'.~r_ Lne an,-. n
q 1!-rfivio' e", Krakow no.'~~ 51_96 16,,,2
r w

I

YkSzEWF J.; BALA, M.
Heterocyclic analogs of carcinogenic hydrocarbons; tetraly-I
derivative of benzo-diazaanthracene. Bul chim, PAN 12 no.6:
393-377 164.
1. Department of Organic Chemistry of Jagiellonian University,
Krakow. Submitted April 8, 1964.

MSZEW. J. I SLEDZIEWSKA, E.
Reaction course of the ety-nthesl -i of benzodiaza&nthracene derivatives
an determined by the type of triarylguanictine uned. Bul chim PAN
12 no.6099-402 164.
1. Department of Organic Chemistry of Jagiellonian University,
Krakow, end Laboratory No.6 of the Institute of Organic Synthesis
of the Polish Academy of Sciences. Subritted April 8, 1964.

MOS2EW1 J.; ZANKOWSKA-JASINSFA, W.
Heterocyclic &"logs of the carcincgenic hydrocarbons; derivatives
of 1,2-banzo-3,9-diazaanthracens with mono-and polyoyclic substitutes.
Bul chim PAN 12 fio.6s403-406 164.
1. Department of Organic Chemistry of Jagiallonian Universitv,
Krakow, and Laboratory No.6 of the Institute of Organic Synthesis
of the Polish Academy of Sciences. Submitted April 8, 1964.

MOSYN, J.; '"'ANKOWSKA-JASINSKA, W,
Characteristic isomerism anti transformat!.-,nq -~ lerIvatives --f
1,2-benzo-3,9-diazaanthracene. Bul rhim ?.AN ro.7:,'4"-450 '64~
Ultraviolet spectra of the heterocyclic ax-ilogs from carcincgen--'r
hydrocarbons, Ibid.:455-458 164.
1. Department of Organic Chemistry -f :agie'lon' - 11%iversity,
Krakow, and Laboratory No.6 of the Ins.1bite of Orgar. -- Synthesis
of the Polish Academy of Sclences, -,bmitted April 8, 1964,

mosmw' J.; ZYMMISKA, T.
An'.hracenyl derivatives of iiiinoline ard benzodiazaainln-scen-e.
Bul chim PAN 12 n0.7:451-454 f64.
1. Department of Organic "'heml5try of Jagiallonian University,
Krakow, Submitted April 8, 1%Y_

MOSZEW, J~; SLED ZI ~:WSK A, F,
Absorption capaclty of cumpounis of tne 1.2-r.Pnz---
diazaanthrRcene groap in the ultraviolet, Bid cKim. P.IJI
12 no.9:507.-510 161..
1. Department of Organic Chemif?try of Jagial lori,ar; Tj-,!ver:,.Ity,
Krakow~ 3ubmitted April 8, 106,~,

41