SCIENTIFIC ABSTRACT URBANSKI, T. - URBANYI, L.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001858020016-0
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: April 3, 2001
• Sequence Number: 16
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

URRANSKI, T. .; tI-RILKa, J.; ECKSTEIN, "I'.
Some problens of obtaining weed, killers. XIII. Preparation of 5-n-Itro-5-
hydroxyrethyl-3-phenoxyethyltetrahydro-1, .3-oxazine. P. 519
ROCZNIKI ClffaI. (Polska Akaderda Nauk) Warszavas Poland, Vol. 33,, no. 2. 1959
Monthly Ust of East European Accessions (FEAI) W$ Vol. t., No. 9., -Septerber 1959.
Uncl.

Distri 4E3d
improved aparation. .1
.1LIki, juliusz
Hackel. Stama&.w Mortka, Kazimieri-523'C~MvialRO-s-
Z=- Slebodjja-sR,-.-;!p-d-Wleslaw Witek jKateura I-ech- Tw)
R. Organi"nei 11 Politecb, UIM=aw. 'Prseftlys) Chm.
38, 651-4klQ59)t--NitMtIon ot I mote tolutne with a ndxt. -T ~V
of 1.3 motes HN03 (d. 1.52) and 1.75 motes ActO (10% 2
hrs.) gave the mononitration product (1). not (or only
slightly) contaminated with the meta isomer. I was further
nitrated to di- and trinitrotoluene by usual methods. The
purity of the raw trinitrotoluene so obtained wasclaitued to
be sufficiently high to be used as an explosive without addni.1
purification. Michatillsk-i

URBANSKI, Tadeusz: GLUZINSKIq Przemyslaw
Exchange of halogen for halogen in ame o6 - chloroacetic acids. Rocz
chemiA 33 no.4/5:1031-1037 '59- (MI 9:9)
1. Katedra Technologii Or anicznej II Politechniki, Warszawa.
(Chloroacetic aciZ (Halogens)

UPJMSKI, Tadeusz: CHIMLAKp Andrzej; ECKSTEIN, Zygmunt
11 ------------
The products of the reaction of methyl. 2-hydroxy-)-naphthoate with
formaldehyde and cyclohexylanine or benzylamine. Rocz chemil 33
no.4/5:1201-12o6 59. (EEAI 9.19)
1. Katedra Technologii Organicznej II Politechnikig Warszawa.
(Hydroxymetbylnaphthoate)
(Formaldehyde) (Cyclohexylamine)
(Benzylamdne)

URBANSKI, Tadeusz; SKOWRONMA-SEWINOWA, Barbara; CHADZYNSKI, Grzegorz
------------
Reactions of aromatic amines with cyanoguanidine. VIII. Reactions of
arylamidine ureas with amines. Rocz chemii 33 no.6:13)2-1341 159.
(EKAI 9:9)
1. Katedra Technologii Organicznej II Politechniki, Warszalla i
Zaklad Syntezy Lekow Instytutu Gruzlicy, Warszawa.
(Amines) (Cyanoguanidiyie) (Aryl groups)
(Aromatic compounds) (Amidinurea)

0 ,
URBANSKI, Tadeusz; SKOWHONSKA-SERAFINOWA, Barbara;*LOWSRI, Jerzy
Reactions of aromatic amines with syanaguanidine. IX. Naphthalamidine-
urea and its reactions with amines. Rocz chemii D no.6:1377-1382 #59,
(MI 9:9)
1. Katedra Tecnologii Organicznej II Politechniki, Warszawa i
Zaklad Syntezy Lekow In3tytutu Gruzlicy, Warszawa.
(Cyanoguanidine) (Amines)
(Naphthylamidinourea) (Aromatic compounds)

URBANSKI, Tadeusz; SKOWRONSKA-BERAFINOWA, Barbara; MATUSIAK, Arkadiusz;
Adam; ZARUKIEWICZ, Maciej
Reactions of aromatic amines with syanoguanidine. X. Alkyl and
arylalkyl derivatives of amidinourea. and their reactions with
amines. Rocz chemii 33 no.6:1383-1388 159. (EM 9:9)
1. Katedra Technologii Organicznej II Politechnikig Warszawa i Zaklad
Syntezy Lekow Instytutu Gruzlicy, Warszawa.
(Amines) (Cyanoguanidine) (Alkyl Groups)
(Aryl groups) (Amidincurea) (Aromatic compounds)

HACKEL, -Tu3-iuaz; P~AN~KI,_Tadqussj_ KUTKIEWICZ, Wiealaw; STERNINSKI, Andrzej
Viscosity of mixtures HN03-H2SO4.--H2O. CbemiA stosow 4 no.3A:443.-451
160* (=I 3.0:9)
1. Katedra Technologii. Chem102n8J II Politecbniki Warszawakiej.
(Viscosity) (mixtures) (Nitric acid)
(Sulfuric acid) (Water)

(' - URBANSK 1, -Tadeus.z.-
Separation ofb-amd r,-radopactove iramoi, decau products from
uranyl nitrate by solvent extraction. Chem anal 5 no.2:283-288 160.
(EUI 10:3)
1. Zaklad Technologii Chemicznej Instytutu Badan Jadrowych PAN,
Warazawa.
(Uranium) (Radio isotopes) (Uranyl nitrate)
(Solvents) (Beta rays) (Gamm, rays)

URBUSKI, Tadeuez S.
Potentiometric titration of small amounto of uranim with vanadats.
Chen anal 5 no.41687-689 160. (EFAI 10s9)
1. Zak-I-d Tscbnologii Chomicsnej Inetytutu Badan -Tadrovych PAN,
Warszawa.
(?otentiowtor) (Uranim) (Vaudates)

URBANSKI, Ta
Recovery of uraniuT from leaching liquors by the dedocyl
phosphoric acid extraction method. Nukleonika 5 no.MS31-843
16U.
1. Instytut Badan Jadrowyeb,, Warszawa$ Zaklad Technologii
Chemicznej

U ff- 13A /V,5KI, T.
atrt qx d
if N11TO&M of tolueselln tbe Presence of Chromic "U.
Uftfiski. A. WRkW%uk. S. CJozak, and T.
--yWojftuwa a. scs..
:Sir. sd.. Chim.. jeoi. d# maPh. S. 13-114 1 En
-Toluene (,) treaWw HNO, + H%14
2 "InItrobensaidehyde (11) and (or) "IttObt
or 2,4.Mnilrobenjok scW (IV). 1- (10 a.) was added
d- Ise at 25' with vigorous stirring to 21.7 CrIG6 1
I-SOPW9. HSO, (d. 1.84) and 25 g. HNOs (d. 1.511,the green
-mixt. left 1.5 hrs-, poured into 1 1. cold water. the cryst.
ppt. filtered off, washed with cold water. dissolved In 200
mi. at.0, shaken with 200 mi. 1017o aq. NajCOj, and crystd.
from a1c. after evalm. of ether to give 6.5 g. U. ToIOg.I'
was added dropwise at mist. temp. 25' a mIxt. of 30 X.
HNO~ (d. 1.40), 90 g. 1-10904 (d. 1.84). and 8 g. H*O slmul.'
taneously with 43.2 g. CrA in Small Portions. the red and
finally green mixt. stirred 2 hrs. at 25*, poured Into 11. cold
water, the ppt. ticated as before, and 3.99 g. III pptd. by
acidifying the sq. layer with dil. ILSO.. To 30 g. HNO~
(d. 1.50). 90 9. HrSOj (d. 1.84). and 8 g. water was added
14.9 g. p-nitrotoluene and 43.2 S. CrjOj at const. temp. 60%
the brnwa and finally green mixt. stiffed tit W 2 hrs., and
treated as before to yield 14.0 g. IV from the aq. layer.
'0 -;.Siecki
YX X

' Wk4
Mand Wits WO-W. AW-t-
T
L,U,d 1~1
Bull. U0.1 am. 1.
CO., WAM
16(f in'
le~
Ckim" led. 09 Se 4P .8, 15-16( in East' ); cf.~
preceding abstr.-M-Dini y (1) the*
.1d.5.
main product of the reaction studied To toluene
to, WAS
a mW N03
slowly added with vilorous stird" o 21 g. H
h I -S
(d. 1.41) and 160 g, anhyd. HtSO4 simul y wit
tirred so
C. fresh MnOk, at 30-40% the light yellow mixt. s
d wl
min., powed Into cold wain, and 6.4 1. crude I ext
Itrotoluents. Stmi-'
'RtgO. It contained tracex of monont
larly, 9.1 g. I was obtained at 700 from 5 g. "itrotrJueae.,
45 1. HAO, (d. 1.84), 39 g. HN03 (d *1.51), and 9.4 g.
Mn0j; at 3G-40* this reaction gave 21% 1 and 7% P-bitro-
benzoic acid with oxalic acid and C02 by-products. The
reaction with KMnOj replacing MnO~ was extremely violent.

wihm Pat-
1- 1' tb* V"-*=*
DApAEOI Awka
1709MVIS English);
pjj~edurc imitar to that demaiW
d.Xrec;:~d'u' 'bt' 0% 2,4-dinitrobestAl'
e pteceffingbst, gave ats"O 3 - VA, 14 S.
de yde( ith 7 . "Itrobenzoic acid with 6 1
H " 0. .84). At 60-700 the,
N d. 1.41 and go S. H.50. (d. I
-70-900 tarry products were
yield .1 .1dhyae as lower; at

URBANSKI., T.; KUCZYNSKI, W.; ANDRZEJAK, A.; HOMAN, W.; WITANOWSKI, M.
Some notes-on methodis of inveotigation of coal in infra- red spectra.
Bul chim PAN 8 no.1:19-22 160. (Mui 10: 9/10)
1. Department of Chemical Technology A, Mickiewicz University, Poznan.
Department of Organic Synthesis Polish Academy of Sciences. Presented
by T. Urbanaki.
(Coal) (Spectrum, Infra-red)

CHIN, r.Ch.; VU, r.x.; SKOWRONSKA-SERLFIN, B.; URBAN-S-K.1,'T.; VENULET, J.;
JAKIMOWSKA, K,
Antimlarial properties of some derivatives of phenjrlmddinsurea. Bul
chim PAN 8 no.3tl09-112 160. (EZAI 10:9/10)
1. Institute of Materia, Medica, Acadevq of Medical Sciences., Poking..
Dept. of Organic Tecbnolog7, Warsaw, Teabnical University and Drug
Research Institute, Warsaw. Presented by T. Urbanski.
(Antimalarials) (Phenylaxtidinourea)

.-URBANSKIP T.) SEMCZUK, A.; GORSKIp W.
Thermal analysis of the "stem: 1-chloro-2,4-dinitrobenzone-vier7I.
chloride. Bul chim PAN 8 no.9:4P-488 160. .'-r
1. Technical Military College, Warsaw. Presented by T. Urbanski.
(Thermochemistry) (Chlorodinitrobenzene)
(Acid chlorides)

URNK~KT,Ta-leusz, prof.dr.
Application of sore p-vsico-chemical methods for stul-les on
the structure of organic comrounds. Wiad chem 14 no.3:137-
355 Mr 160.
1. Kierownik Katedry Technologii Chemicznej Organicznaj II, Foli-
technika, Wroclaw, I. czlonek rzeczfwisty Polskiej Akademii Nauk,
Varazawa.

URBA19SKI Ta OVA, Barbara; GUSTOWSKI. Wlodzimiers;
Krystyna; JANOWIEC, Hiecsyslav
VENULET, Jan; JAKIMOVSKA,
Anti-tuberculous properties of ethyl acatoacetate isonico-
tinoylhydrazone (T-428). Gruslica 28 no.12:955-960 D 160.
1. Z Iratedry Technologii Organiesnej II Politechniki Warazavakiej
Kierownik: prof.dr T.Urbanski i z Zakladu Parm&kDlogii Instytutu
Lekov, Kierownik: doc.dr J.Venulet.
(ISOBIAZID rel apda)

SKULSKIP Lech, mgr. inz.; URBANSKI, TdeuBz
On the absorption spectra of azo dyes. I. Spectra of azo dyes
deriving from 4-bydroxy- and 4-acetoxyazobenzone. Rocz chexii 34
no,13141-157 160. - (EFAI 10:9)
1. Department of Organic Technology II, Institute of Technology,
Warsaw.
(Absorption spectra) (Azo cIompounds) (Isobenzene)
(Acetoxy group) (Phenyl&2ophanol)

SKULSKI, Lech; URBANSKI, Tadeusz
Reactions and the absorption spectra of con dB derived from
v-nitroBtyrens. I. On the preparation of /#P- (3-nitrovinyl)- anolim.
Rocz chemii 34 no.1:283-287 160. (EKAI 10:9)
1, Department of Organic Technology II, Institute of Technology,
Warsaw.
(Absorption spectra) (Nitrostyrone)
(Nitrovinylaniline)

SKULSKI, Lech.; URBANSKI, Tadeusz
Reactions and absorption spectraof compounds deriving from uol-nitro-
styrene. Pt.2. On synthesis of azo dyes with a 6-nitrovinyl group.
Rocz chemii 34 no.2:431-441 6o. (EEAI 10:1)
1. Katedra Technologii Organicznej II Politechniki, Warszawa.
(Absorption spectra) (Azo dyes)
(Nitrovinyl group) (Nitrostyrene)

SKULSKI, Lech~ URBANSKI$._Tadeusz
On the absorption spectra of azo dyes. II. Spectra of derivatives of
4-formyl-, 4-nitro-, and 4-(,B -nitrovinyl)-azobenzene. Rocz chexii
34 no.2:443-455 160. (FRAT 10:1)
(Absorption spectra) (Azo dyes)
(Forwjlazobenzene) (Nitroazobenzene)
(Nitrovinylazobenzene)

GURNE, Daniela; URBANSKIp Tadeuaz
Reactions of aliphatic nitro compounds. XLIV. Conformation analysis
of the derivatives of 5-nitro-3-alkylo-3-cyclohexyletetrahydro-1,3-
oxazine. Rocz chemii 34 no.3/4:881-886 160. (EMI 10:3)
1. Zaklad 57ntezy Organicznej Polskie Akademli Naui, Warszawa.
(Nitro group) (Alkyl grou i
(Cyclohoxyltetrahydrooxazine)

ECKSTEIN, Zygmunt; GROCHOWSKI, Edward; :J!T~!~SKI,, Tadeusz
The fungicidal activity of derivatives of 2-nitropropanediol-10.
Rocz chemii 34 no.3/4;93i-94o 6o. (EW 10:3)
1. Zaklad Syntezy Organicznej Polskiej Akademii Nauk, Warszawa
(Nitropropanediol) (Fungicides)

URBANSKI, Tadeusz; FALECKI, Jerzy
1~
Experiments with hydroxamic acids. VII. Nitration of ar7lb7droxamic
acids. IT. Rocz Chemil 34 no.5-'1283-1296 160.
(EUI 10: 9)
1. Department of Organic Technology, Institute of Technology, Warszawa,
and Institute of Nuclear Researchs Warszawa.
(Hydroxamic acids) (Aryl groups) (Nitration)

SKULSKI, Lech; URBANSKI, Tadeusz
Reactions and absorption'"ctra of compounds deriving from IV -nitro-
styrene. IV. Absorption spectra of W -nitrostyrore and its para-
substituted derivatives. Rooz ebemii 34 no.5.'1107-1328 '60.
(EM 10-9)
1. Department of Organic Technology II, Institute of Technology,
Warszawa.
(Absorption spectra) (Nitrostyrone)

CZERWIRSKA, Elzbieta; ECKSTEIN, Zygmunt; HETRARSKI, Bogumil; KOWALIK,
Romuald; URBAITSKI,,Tadeuss
On the biological activity of some alkvl- and arylmercury haloides.
Przem chem 39 no.4:222-225 Ap 160 .
1. Zaklad S)mtezy Orgamicznej, Polska Akademia Nauk, oraz Instytut
Przeryslu Organicznego, Warszawa.

URBANSKI, Tadeusz S.
Cation exchange solvent extraction of iron. Nukleonika 6 no.4:299-
308 '61.
1. Instytut Badan Jadrowych Polskiej.Almdemii Nauk, Warszawa,
Zaklad Technologii Chemicznej.

URBANSKI, Tadeusz S.1 MINC, Stefan
Solvent extraction of cations with al~fl phosyjyric acids fro= sulfate
solutions. I. Solvent extraction of U and F with dodec7l phosphoric
acid in the presence of different cationB. Nukleonlka 6 no.12:765-773
161.
1. Institut yadernykh issledovanly PAN, Varshava, Laboratoriya
khimicheskoy tekbnologil. Varshav6y universitet, Kafedm fizicheskoy
khimii. I

URBANSKI, T.
I - -- -----
-1 colour reaction of primary nitroparraffins. Bul cbim ?AS 9 no.5:
319-320 161.
1. Institute of Organic Synthesis, Polish Academy of Sciences*
(Nitrogen compounds) (Farraffins)

URBANSKI. T.
On a new colour reaction of nitromethane and some aromatic nitro-
compounds. Bul chim PAN 9 n0-5:321-322 161.
1. Institute of Organic Synthesis, Polish Academy of Sciences.
(Nitrogen compounds) (Methane) (Chemical reaction)
(Aromatic compounds)

BOMkIj Z.; URBANSKI, T.
Chi preparation of 2,46.,-trinitrophenylacetic acid. Bal chim PAN 9
no.7:461-462 161.
1. Military Technical College, Warsaw. Presented by T. Urbanski.

BONECKI, Z.; URBANSKI, T.
On preparation of 2,4,,6,-trinitrostyrone and oome 2,4,6,-trinitro-
phenylethane derivatives. Bal chim PAN 9 no.7:1#63-1,66 161.
1. Militar7 Technical College, Warsaw. Presented by T. Urbanski.

URMSKI.-T,- SEMENCZUK, A.; GORSKI, W.
The action of ultraBon-ic waves on nitration. Bul chija PAN 9 no.73
467-469 161.
1. Military Technical College, WarBaw. Presented by T. Urbanoki.

SURNIME, Given Nums
Countr-Z: Poland
Academic Degrees t
Affiliations
Satsrces Warsaw, Ppstepy HIRIeny i Medycyny Dosvindezaloll, Vol XV9 No 1+2
1961, pp 427-428.
Datas "Antineopla3tic Properties of Derivatives of Oxazines"
English abstract of article originally published In Wature, 1960
187,.426.
Authors-%-----
URBANSKI T
Prof . Dr., Director of the Mudwik Hirszf eld Inst-
of Immunology and Experimental Thiebl%py (Instytut Immunologii i
Terapii Doswiadczalnej im. Ludwika Hirszfelda), Polish Academy
Sciences (PAN--Polska.Akademia Nauk), Wroclaw.
GUM . D.
R5~SKAI H.
CW=SKAIB.
)(TRAmKis, M*

S/06 62/000/02"k/040/120
B166YBIOI
AUTHORS: Serafin, Barbara, Urbdn'ski, Tadeusz
TITLE- Reactions of amines with cyanguanidine. Part XI. Hetero-
cyclic derivatives of amidineurea
PERIODICAL: Referativnyy zhurnal.. Khimiya, no.-23# 1962, 294-295,
abstract 23Zh234 (Roczn. chem., v.'36, no. 4, 19621 679-683
[Eng.; sui-maries in Pol. and Russ.))
TEXT: Hydrolysis of biguanides RRINC(.NH)NHC(-NH)NH (Ia-d;'(a) R - H,
2
R1 - quinolyl-6; (b) R = H, RI - quinolyl-8; (6) RRIN - morpholino;
(d) RHIN - piperidino) with dilute HCl gives t~e corresponding
amidineureas RR'NCONHC-(_NH)NH 2 (IIa-d). In the same way piperazine-bis-
biguanide (III) is converted into piperazine-bis-N-formylguanidine (IV).
IIa, b hydrochlorides with boiling aniline form guanidine, CO(NHC 6H 5)2 and
6- or 6-aminoquinoline respectively, probably via the intermediate formation
of the corresponding I-quinolyl-3-phanylurea. 2 g Id hydrochloride in
Card 1/3

S/081/62/000'1023104C-112.)
Reactions of amines with... B1661.B101
20 ml 3 N HC1 are boiled for 30 min, cooled, then Ila dihydrochloride
C H N 0-2HCI, is separated, yield 65/4, m.p. 171-173c)C (from alcohol~;
11 11 5
Ha, m.p. 200-2020C (decomposition; from water); monopicrate, m.p. 242-244OC;
dinitrate, m.p. 203_204 0C are also separated. 8-aminoquinoline,
oyanguanidine and 3 N HC1 (0-017 moles each) are boiled for 2 hrs giving
Ib hydrochloride, C11H 12 N6*HC1, yield 80~, m.p. 243-2450C (from water);
Ib, m.p. 163-i650C (from water; dipicrate, m.p. 210-2110C. 0.1 mole
piperidine hydrochloride and 0.1 mole cyanguanidinA are heated for 3 hrs at
130-1400-u-,' they-are'--then grourt product
is Id hydrochloride, C H N *HC1, yield '10,1, m.p. 205-2070C (from alcohol).
7 15 5
Ila are produced in the same way, as follows (order of data: initial
substance, products, gross formula of baseo yield % hydrochloride,
melting point OC of the base, the hydrochloride and the picrate):
Ib hydrochloride, N
-(solution half BvApcEqted), Ilb,.Q H 0, 70, 158-160
11 11 5
(from'wate~ -t, 235--,~A d composition);
r)', e Ic.hydrochldride (12% HC1, boiled
45 mint cooled 0 500 t 50 ml acetone added),,IIC, C H N 0 , 60, 178-179,
i. 6 12 4 2
216-220 (from 50% 4cetone), 212-213; Id dihyd~ochloride (12% Hol, boiled
Card 2/3

Reactions of amines with...
S/08 62/000/023/040/120
B166XB101
30 min and water removed by vacuum distillation)j.,Nd, C7H14N40, 72,
176-177, 203-205, - 15 g III hydrochloride are boiled for 45 min in
45 ml 12% HC1, this is cooled and alcohol is added separating IV dihydro-
chloride, C8H16N80 2. 2HC1, yield 60%, m.p. 237-2390C (from dilute alcohol)l
IV, m.p. 199-200OCi piorate, m.p. 223-2240C; dinitrate (from the,dihydro-
chloride and 50% HNO3), m.p. 200-200C (alqohol precipitated). For part
X see RZhKhim, 1960, no. 18, 73392. [Abstraicterlo note: Complete
translation.]
Card 313

S/081/62/000/024/036/073
B-1 01 /B1 86
AUTHORS: Calus, H., Eckstein, Z., Sob6tka, W., ~E~
TITLE: Endoisomers and exoisomers of nitroolefins (1-cyclohexenyl
nitromethane and oyolohoxylidene-nitromethane).
III. Measurement of dipole moments
PERIODICAL: Referativnyy zhurnal. Xhimiya, no. 24, 1962, 2769 abstract'
24Zh8 (Bull. Acad. polon. sci. Se'r. sci. chim., V. 91
no. 11, 1961, 725-729 [Eng.; summary in Russ.])
TEXT: Dipole moments were compared to explain the composition of a
V
mixture of cyclohexylidene nitromethane (I) and cyolohexene-1-yl.nitro-
methane (II) forming when 1-nitromothyl-l-hydroxyoyclohexane (IIIJ is
I
heated. Results: (CH2)4 C(CHRN02) - 6H, (where R - H, CH 3' and C2H Of
(6H2)nC(CH2NO2) - 6H (where n w 5,6), nitrocyclohexane, cyclohexyl nitro-
methane, and 1-nitromethyl-4-methyl-cyclohexene-l*were found to have the
same dipole momenta of 3.6 (+,O.ID). The dipole moment (4-3D) of the
Card 1/2

S/081/62/000/024/036/073
Endoisomers and exoisomera B101/B186
mixture obtained from III indicates the predomina"nee of substance I with
C=C bond with the nitro
a higher dipole moment due W.conjugation of the
group. Determination o? thq 4ipole moments of mixtures produced by
adding different amounts of 11 to the reaction mixture leads to the
assumption that the content of the exoisomer I in the reaction mixture,
is 901A being consistent with the data of the IR spectra. Communication
II see RZhKhim# 1958, no. 3t 7680. Complete
EAbstracter's note:
translation.]
Card 2/2

URBANSKI, Tadueaz S.
Device from the extraction of liquids in a thermostat.
Nukleonika 7 no.1:50-51 162.
1. Instytut Badin Jadrowych PAN, Warszawa, Zaklad Technologii
Chemiaznej

URBANSKIY,, T. (Urbanski,, Tj, prof. (Pol'sha)
Conforwtion of certain heterocyclic compounds. Zhur. VKHO 7
no.4:396-400 162. (MIRA 15:8)
(Heterocyclic compounds) (Stereochemistry)

URBANSKI, Tadeush S.[Urbanski-,-Tade-usz-S-j; MINTS, Stefan [Mine, Stefan]
Extraction of cations with alkyl phosphoric acids from ffulfate
solutions. Pt. 2. Nukleonika 7 no.11003-713 62.
1. Institut yadernykh i3sledovaniy PAN, Varshava, Laboratoriya
khimicheskoy tekhnologii Varshavskiy Universitet Kafedra
fizicheskoy khimii, Varshava.

URBANSKI, T.; PISKORZ, M.; GETNER, W.; MACIBJEWSKI, M.
Theizal analysis of tetranitromethane mixtures with be4ene AM
nitroaromatic compounds. &i1 chim PAN 10 no.6:263-266 162.
1. Technical Military College, Warsaw. Presented by- T. Urbanski.
i I

ECKSTEIN, Z.; GLUZINSKII P;; PLEITKIEWIGZ, J.; URBANSKI, T
on the contribution of hezahydro-o-triazines in the synthesis zechanis=
o:r,5-nitrotetrahydro-l,,3-exazine derivatives. Bul chim. PAN 10 no.9:
4&k9Z 162.
1. Department of Organic Technology II, In3titute of Technology,
Warnav, and Institute of Organic bynthesis~ Polish Academy of
Scien.ces, Warsaw. Presented by Ur~anski.

URBANS.KII T..-, ..
The 18th Congress and 21st Conference of the International Union
of Pure and App3ied Chemistry. Wiad chem 16 no.ls5O-52 Ja
162.

---URJ3ANSKI, T, -
Thle hundredth anniversary of Butler's theory of the structure
of chemical compounds. Wiad chem, 16 no.7t467-471 Jl 162.

URBAHBKI, T.
nPure and applied chemistry.* Reviewed by T. Urbomaki.
Viad chem, 16 no.8t533 Ag '62,6

MMMKI 0 T.
V~
Prof. Wolfgang Langenbeck became honorary member of the
Polish Chemical Society. Viad chem 16 no,12:776-777 D 162.

URBANSKI, Tadeusz, prof.dr.
"Fare and applied chemiatr7-0 Reviewed by Tadeu3z Uzibansski.
Problemy 18 Jc2.

URBANSKI, Tadeusx, prof. dr.
Distiaotion of an outstanding ahemist, Probl*aV 112 r4.7:52,2
529 162.
1. Calonelc rzeazywisty Polskiej Akademii Nauk, Warszawa.

SERAFIN, Barbara; UFJ3AI,'SYJ, Tadeusz
Reactions of amines with cyanguanidine. Pt.11. Rom chemii
36 no.4:679-683 162.
1. Dopartment of Organic Technology II, Institute of Technology,
Warsaw.

SKUWKI $ Lech; aW~S ~Tadeu~
Absorption spectra of azo ayes. III. Rocz chemii 36 no.5:
801-820 162.
1. Department of Organic Technology II,, Institute of Technologyo
Warsav.

URBANSKIp Tadeusz; EELZECKI, Czeslawl ECKSTEIN, Zygmunt
41 -- -
Reactions of nitroparaffina, Pt, 48, Rocz Cbezil 36 no,5:
879-M 162,
le Department of Organic Technology Ill, Institute of Technologyy
Warsaw,

IANGE, Jerzy; URMINSKI, Tadousz; I&INJUT, Jan
tz"~~
Preparation and biological activity of the derivatives of
phenylsuccinic acid. Fts.2-3. Room-chemii 36 no.11.1625-1638 162.
1. Department of Organic Technolgy 11, Institute of Technology,
Warsaw.

1ANGE, Jerzy; UW.11SKI, Tadouuz; VENUILT, Jan
Preparation and biological activity of the derivatives of
phenylsuccinic acid. III- Rocz chemli 36 no.lltl631-1638 162.
1. Department of Organic Technology 11, Institute of Technology,
Warsaw.

URBANSKI,, Tadeusz S.
Onthe possibLlity of deircning alumimm mulphate by
extraotton with alkylophosphoric acids, Frzem chem
41 no.4:19~-201 Ap 162.
1. Zak3md Technologii Chudezvej Instytutu Badab
Jadronchp Warszmo

URBANSKI, T,
NPure and applied chemistry." Reviewed by T.Urbanaki. Frxem
chem 41 no.6:3" Je 162.

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---------
Formation of tetranitromethane from nitroform and nitryl chloride.
Biul chim. PAN 11 no.2:77-78 163.
1. Technical Military College, Warsaw.

PISKORZ, M.;_TJRBANSKIV T.
...
Ultraviolet and infrared spectra and structure of isonitramines
(nitrosohydroxylamine derivatives). Bul chim PAN 11 no.11;
597-606 163,
Ultraviolet and infrared spectra of some nitrosamines.
lbid.t6O7-624
1. Technical Military Collpge, Warsaw. Presented by 1'. Urbancki.

ECKSTEINP Z.j GROCHOWSKI, E.; KOWALIK, R.; URRANSKIV T.
F"gicidal activity of arme 2-ni trop.-cpaned 1-1, 3-ol dbrivatives.
Bul chim PAN 11 no.12t687-693 163.
1. Institute of Organic Synthesisp Polis4 Academy of Sciences,
and Mycological Laboratoryt Institute of Orga a Chemistry, WRrsaw.
Presented by 1'. Urbanski.

URBANSKI, Tadeuezi rof. dr
Metabolism of MbaUdomide. Problemy 19 no.1:4&47 163,
I* Czlonek rzeczywisty PoIsUej Akademii Nauk.. Warszawa.
-9-

MLBM,U,,_T&Aquosv prof. dr
phplciot or ehelaioto LroblojnY 19 r'0.4z264 t63-
1. politechrAkap Warazaida.,

URBANS~~OIRP-S-J, -prof. dr obleMY 19
International debates of chemists in London. Fr
no.los640-643 163.
1. czlonek rzeezywistY Poiskiej Akademii Naukv Warszawa.

GVSTMKI, Wiodsimleria; -UR-BkML14 ladewo 7-4642 163.
Furan derivatives* pt. 1. ROCS Chsmii 37 no.4:43
1. 1.nstituts Of Organic Synthesio.9, pO3_jsh AcadeuV Of Sciencesil
Warsaw&

DABROWSKA, Urszula; URBANSKI, Tadeusz
Infrared apectra of nitrophenolls and interna hydrogen bond bet,---en
Plienoll-c and nit,ro groups. Rocz chemii* .37 no. 7/8:805-817 163.
1. Institute of Organic Synthesia, Polish Academy of Sciences,
Warsav.

th'L,, In,,;t Lut of C c
I'm-uq 0 zzof t1w Pblica 'kc'!" a7pa' of 'jc-~cnccs S)yntt~,Ly
a), in -.jarsa-.:.
Alcadu-ali Uat~: kr3n j, -
llc-.r 1:uthod of li-c-naration of 'Jon,. Lc:70
,O,qr Zoc;zn--":I C!,,,: Vol 7 9, :Lgr)-, pp. 1073-107-5.
Abn,traab: f"Ut!10:-~11 ::nziish a ncw
no-thod o.- -,)r~marj-pg icaddfal'-yl salt2. Tlh~ conslstk,:~ in
J.
amicuar, or acetone colut-ion of 1cad,
a:; Ih- -viccd -=d'
,..,c r c ' -121-y1). A =7,scst.cd nv-~--od J - d:,
a machmin-ri of -'I.Iio dc.,cribcd raact'*Lom is rcferoncec,
onc Polio'.ij md 3
16 -

PHASE I BOOK W LOITATION POL/6347
(6348,6349~
Urb"DLngki, -Tadousz, Doctor, Profeefjors and Correoponding Member,
Tbolisiiko-016~cr Sciences
Chemia, i technologia materia;e~w wybuohowyoh (0aartistry and
Technology of Explosives) j v. Warszawa, W14ONs 1954. Errata
slips inserted. 5000 copies printed.
Reviewer: W. Cybulski, Professor, Doctor, and J. Hackel) Professors
Doctor; Ed.: J. Jurecka, Master of Engineering; Tech. Ed.:
H. Malazewska.
PURPOSE: This book is intended for graduates and postgraduate
students specializing in the chemistr-j and technology of
explosives, for scientists, and for engineers working in the
production of explosives.
Card l/V

Chemistx7 and Tichnology (cont.)
POL/6347
(6348,6349)
COVMGE-11 This book is a three-volume manual which covers the
physical and chemical.properties of explosives, the mechanism
of synthesis reactions, and the methods for the preparation
of explosives. The.text is basedlon Soviet and non-Soviet
sources and includes works by the.author; some of which are.
unpublished. References are given separately at the end of
each volume. Volume 3 includes an author Index and a subject
index to all three'volumes.
TABLE OF CONTMMS [Abridged
VOLUME I..
Foreword
'Classification of Explosives
Card 2/$

KATCKA, M.; URBANSKI, T.
Infrared abso-ption spectra of Quaternary salts of pyridine.
Bul chim, PAN 9(i.e. 12] no.9:615-621 164.
1. Institute of Organic Synthesis nf the Polish Academy of
Sciences, Warsaw. Submitted July 3, 1453.

ECKSTEIN, Z.; GLIJZIN3KI, P.; URBANSKI, T.
Some remarks on the Senkus method f-r synthesis of 5-nitro-
tetrahydro-axazine. Bul chim PA.Lb e. 121 no.9:623-626 164.
1. Department of Organic Technology II of Warsaw Technical
University and Institute of Organic Synthesis of the Polish
Academy of Sciences. Submitted July 31, 1964.

URBANSKI, Tptdeusz
Twenty-second Tnternational Conference of the International Union
of Pure and A-Dplied Chemistry. 19th International Congress of
Pure and Applied Chemistry in London. Nauka polska 12 no.1:114-119
Ja-F f64.
1. Member of the Polish Academy of Sciences, Warsaw.

a t
mp
phy.c%4coChemical tjjc)cl:; In
jq Tp
-i8 -221-3
I.. j!,iTbcr of t-116

URBANSKI, TadeuBz, prof. dr.
I.".
~ j'
Polymers; Nobel prize in chemistry, Problemy 19 [i.e. 20)
no.IP~%-57,. 164.
1. Czlonek rzeczywisty Polskiej Akademii Nauk.

j,,jc;fnber of the s'! 1 e r; .3 lie Z-;
of
OF
De,-:W-crnent o-f
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URBANSKI, Tadeusz,... prof. dr
- of natural products. Proble7y 20
Symposium on the chemistry
no.71440-442 164.
1. Member of the Polish Academy of Sciencesp Warsaw.

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MTANSKI, W.
"Voice from the construction site of a hydroelectric plant," Gos.podarka 1~:odna,
Warszava, Vol 15, No 1, jan. 1954, p. 30.
SO: Eastern European Accessions List, Vol 3, No 13., Nov 1954, L.C.

URUNSKI, Wieelaw (Poznan, u1. Krasinskiego 10.)
Role of novocaine blocks in the treatment of acute necrosis of the
panGreas. Polski tygod. lek. 12 no-34:1303-1307 19 AU,' 57.
(Z III Kliniki Chirurgicsnej A.M. w Poxnaniu; kierownik: doe. dr
Jersy Boratewski)
(PANCRUTITIS, therapy.
procaine nerve block (Pol))
(PROGAIN-3, therapeutic use,,
pancreatitiog nerve block (Pol))
(ANIMSTHISIA. WIOULL, in various diseases,
procalne block in pancreatitis (Pol))

-.-URBANSKI_, Viodzimierz, mgr inz.
From the activities of the Kielce branch of th'i Polish ABBOciatiOn
of Sanitation Engineers and Technictans. PrzegI techn no-52:8 30 D
162.
1. Przewodniczacy Zarzadu Oddzialu Polskiego Zwiazku Inzynierow i
Technikow Sani*mych, Kielce.-

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URBANSKI, Zenon# mgr inz, (Warszawa)
Industrialization of the aangarian construction industry*
"gl budowl i bud mieszk 35 no.112626-628 F163.
CoUcquium of the Inteivatioral Association of Social
Security held in Arsaw. 629

URBANSKI, Zenon, mgr inz. (Werazawa)
- . 11
The husan factotAn tafety problems of building. Przegl Ividowl i bud
rki~szk 36 no.3tl67-169 Mr '64.

-URBANSKIY, K.S.
Faergency excitation network of the auxiliary g6nerator. Elek. i
tepl. tiaga 6 no.1106 N 162. (MIRA 16-.1)
1. Mashinist-instruktor depoChalkar Kazakhskoy Vorogi.
- (Dis"l locomotives) ,

U.S.S.R. / Human and Animal Physiology. Liver. T
Abs Sour: Ref Zhur-Biol., No 5, 1958, 22294.
Author ,-UXbanuk, K G
Inst :Nor~~e~r~-"
Title :Experimental Production of Cirrohsis of the
Liver and Spleen in Dogs.
Orig Pub: Vrachebn, Delo. 1957, No 7, 763-764.
Abstract: Fifty-six injections of CCL4 In a dog, (0.05 mg/
/kg daily) produced distrophic chan[,es in the
liver and fibrosis of the spleen. Following
des ruction of innervation and injections of
CC11 in another dog, development of connective
tissue was noted not only in the spleen but also
in the liver. Severe functional impairment of
of the central nervous system creates favorable
conditions for the development of cirrhotic chan-
ges in the liver through action of toxic agents.
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