SCIENTIFIC ABSTRACT WETZLER, I. - WEYROCH, J.

• Document Type: CREST
• Collection: Scientific Abstracts
• Document Number (FOIA) /ESDN (CREST): CIA-RDP86-00513R001961520019-7
• Release Decision: RIF
• Original Classification: S
• Document Page Count: 100
• Document Creation Date: November 2, 2016
• Document Release Date: September 1, 2001
• Sequence Number: 19
• Publication Date: December 31, 1967
• Content Type: SCIENTIFIC ABSTRACT

HO,Z,A, Frantisek, inz.; WETZLER, Pavel, inz.
A complex study of boring technology development. Geol
pruzkum 6 no.9:262-263 S 164.
1. Central Geological Office, Prmgue; State Commission for
Development and CoordinatLon of S3ience and Technology, Prague.

ME=

f

11-MORSK.I. Stefan, dr in3.
`cat
Economizing --teel in the '"ght, of requirere3rts of i,-,n
rules.. Bud okretowe Warsvvia 10 no.3.,79, innart A,B-(;,tj Mr 165.
1. Gdansk Technical Unluvernity,

-ICERHA MEDICA Sec 18 Vol 3/6 Cardiovascular June 59
1423. Malignant hypertension NadcisnienieZIO',IiAVCSZCZEICLIKL. III Klin.Chorob
Wcu-ne-trznych A. 31., Wroclaw lViad. lek. M8, I VA 1-12 (493-501) Graphi 2
After an introduction concerning the pathology of so-called malignant hypertension,
tile author give!; details of 30 personal cases. The "vssential" form of malignant
hypertension was found in 18 patients, the remaining 12 showing the "secondary"
malignant hypertension during c-r subsequent to a nephropathy. rhe. author finally
gives some therapeutical examp~.es, and states that a simultaneous administration
of hypotensive drugs is advantageous. A distinct remission of all clinical symptoms
(including optiad symptoms) was found only in 3 cases, The improvement was
0
bs, d 2 years after therapy. (XVIII, G-)
e~v~,
-A

CNRIU, A.,; VOINISCU, M.'; SIMICIM. I.,; 01MIU. I..; V_W-Mt B.,;
ANGMLESCU, I.,; RADULISCU, D.,; BUNESCU, G.0; W2ftkkT-z2~R-:--;
LAURI", S.
Preparation of substances inhibiting the development of bacterial
resistance during therapy of tuberculosis and active In therapy
of leprosy. Stud. corcet. inframidrobiol.. Bucur. 6no.1-2sl87L197
Jan-June 55.
1. Institutul Prof. Dr. Is Cantacusino, Sectia do chimloterapie,
Bucuresti.
(TUMMOULOSIS, therap)r
diaminodiphenyl sulfone deriv.,prop. & value in inhib.
of beat. resist.)
(T-PPROSY. therapy
diaminodiphonyl sulfone deriv., prop.)
(SULPOIAS, therapeutic use
diaminodiphanyl sulfone deriv., in leprosy & tuberc.)

OMIU, S..; VOINNSCU, M.,; LUPIJ, A,; MItT. I.,; VXXLXFL, B11
Study of derivatly's of 4immilcotinic acid lWdraside. 1.
is.onicatinoylbydrasone derirativei of ketone &ctds. Dal. stijnt.L
sect.' nod. .7 no.2.657~-563 Al)r-june. 55
1. Moubm corespondent &I A(ademisi M. (for Oeriu)
(HTDWIlJM,* derivatives
isonicotinoy1hychuzono deriv. of ketone acids, chem.
study
(MrIM ACIDS
same)

WHERE =ms=
I Country
cato-t-.;ry
Abs. icur
Author
instit,ut.
Tltla-
Orlr~ Pub.
1.;'ibstract
I
Card:
RUMANIP.
Organic: Chemistry. Synthetic: Organic Chemistryl
Ref Zhw M%JZ-, No 5, 1959, No. 15357
Oierlu, S.; Voineseu, M.; Wexler, B.; Gloter,El
I
Synthe.-iis of Some Asymetrically Substituted 1
Thioureas with Potential Tuberculostatic Acti-I
vity Report I
Studli si cereetari chim.,, :L958, 6, Nc) I.,p
155-16o
With the purpose of investigating the tubercu-1
lostat~ -c activity (TA), 4-ROC 6H4MCSNHCH2CH= '
C112 (I i (where ~ R =C,31 (E) 02 R5-0 CH2 =CHGH2f f
a) CA, S 04H9, (D iso-G4H99 (1) G8H 109 and 4-
C2H50Cj~14'NHCSNHR (II) (where R=3,4-diraethyl-
isoxazolyl--2) were synthesized. Synthesis of I
is aeacmplished by boiling 4-ROC6"4. NH2 (III)
with CJ12=CHCH2NGS (IV) in GH 3OH. I, quanti-
tie a o,!.k origiinal III IV in g, and CH30H in v1.
1/3

Couratry G
lAbs. Jour Ref Zhur Xhim., ft 5, 1959, No. 15357
lAuthor
I List Itut.
Tltl
Orl-
Pub.
0
0. (from alco-!
,yield of I in mp. of I In
hol) are given: Q 5, 7, 5, 77, 79; 0 26, i49
100o 60t 9Z;(Z 20, 10, 70, 54, 74 (from aqueoun
alcohol); W15, 8.7, 50p 60, 66; ~ 6.5, 3
23,40, ft-85;- 0 9 5.2, 30~ 55.5- 105-10~?
S 3, 1-5, 10, 70, 66-67. Analogous'ly, from,7 g.
4-C2H50COOGS and 7.3 9. of 3,4-dimethyl-
5-aminoisoxazol in 7 ml. of CH OH II Is ob-
tained,yield 40%, M-p- 171-1720 ifrom alco-
hol). TA (in relation to 3trains H 37Rv and H.
2/3

Country G f
Abs. Jclar Ref Zhur Maim., No 5) 19~9) so. 15357
A
lluthar
0,
TA1
Ori,~-; ?ub.
Lbstract in dilutions of 1:180,000
:Ratti) eb.anges with
cont'd. and.1:1,800,000. TA of JI develops In a dilu-
tion of 1:10,000,000.-- V. Skorodumov
Card.- 3/3
-G 31

RUM-IIA Organic Chemistry. Synthetic Organic G
Cheadstry.
Zhurimj K11imiya, No. 15, 1958, No. 50312
Abs Jour Ref.
Author Arventiev, B..; Strul Millexier, H.,, Cahane, D.
Inst
Title Preparation and Study of Some Aryl Thioureas -
IV Oxy and mathoxy- naphthyl Thioureas.
Orig Pub Studil si cercetarl Stunt. Acad. RPR Fil. Iasi.
Chim. 1956, T, JL1, 24-30.
7r
Abstract Oxy-, methoxy and carboxymethoxy derivatives of
-naphthyl thiourea (I) were synthesized. The
toxicity of the prepared substances was studied.
Heating the solution of 1-amino-2 naphthol-
chlorohydrate (II) vilth KH4NCs(III) in glaclal
CH3000H (IV) yielded 2-oxy-I (V). By analogy
4-oxy-1 (VI) was obtained from 1-amino-4-naphthol
chlorohydrate (VII) and,III. Methylation of V
Card 1/4

RU W Ik Organic Chemistry. Synthetic Organic
Chemistry.
Aba Jour Ref. Zhur. Khimiya'~ No. 15, 1958p No. 50312
in order to obtain 2-mothoxy-I (VIII) led to a
formation of a previously syntheal."Ied 2-amino,
nWDhthoxyazole (IX). The latter compound may
L
e also prepared by interaction of V and CrOH2-
COOH in an alkaline medium and by heatinS of al-
coholic solution of V with HgO. 4-methowy
chlorohydrate M or 2-methoxy-l-naphthylamine
chlorohydrate when reacted with III or IV yielded,
correspondingly, 4-methoxy-1 (XII) and VIII.
Reaction between III, 1-amino-4 naphthoxy
acetate (XIII) and IV yielded 1-thiouretedine-4
naphthoxy acetate (XIV), While reaction between
.o