SCIENTIFIC ABSTRACT LEMLEYN, V.G. - LEMPERT, K

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SCIENTIFIC ABSTRACT
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V - cn AUTHOR: TITLE: 20-4-6/60 Lemleyn, V.G. On the Spaces of a Symmetric, Almost Symplectic Connectivity (0 prostranstvakh simmetrichnoy pochti simplekticheskoy svyaz- nosti) PERIODICAL: Doklady Akademii Naak SSSR, 1957, Vol. 115, Nr 4, pp. 655-658 (USSR) ABSTRACT: The present paper examines the spaces of the symmetric, affi- nitive connectivity f-1k which is associated with the non- degenerate skew-symmetric tensor a ij . The fundamental defin- ing property of these spaces is the requirement of the pro- portionality of the covariant differential of the fundamental tensor a.. and its external differential: da 1j a.. 6) aja ak aij + + k Fjk - '1j k - P(X) k i - R x (~~ x Jx x By a cyclical distribution of thio relation with regard to i, j, k P(X) - 1/3 is obtained. By transformation i(~ aij aki Card 1/3 A = (1/3)a T x xil + Yijk (x) is obtained. 20-4-6/6o On the Spaces of a Symmetric, Almost Sympletic Connectivity In this connection a li a. - 8 1 is valid and the ti-k(x" are symmetric with regalr~ to ail index-pairs. The a field of geometrical objects invariantly aBSOCiaFte akwi th the tensor a A. The[-1, are a symmetric, affinitive connecti- vity and the" 8ccurring in it define the "rig" of the manifold on whicVkhe tensor a.. is assumed. A differentiable manifold with 2n dimensions wili a non-degenerate skew-sym- metric tensor aig assumed on it and with the object k defining the ri 11 is here designated as "space fsvw- metric, almost symplectic connUtivity". Thereafter the ten- sor of curvatur e R' _ar~k + ijk TX_U__ 6XI k IiB k f,-7, is investigated. In the case B iA.,kl = 0 one can go over to the Cartesian system of coordinate he spaces cor- responding to the case B - 0 can be called plane space3 with symmetric, almost sy'Abfiectic connectivity. Every point of the plane manifold can be associated with a plane space of the type shown here. Finally the covariant vector b Card 2/3 - (1/2)apq Tpqi is investigated. AUTHOR: LEMLEYN, V.G. (moscow) 20-5-7/54 TITLE: _ihe Tensor--oT Curvature and Some Types of Spaces '.'.,'ith Syn- metric Almost Symplectic Connection (Tenzor krivizny 4 ne- kotoryye tipy prostranstv simmetrichnoy pochti simplekti- cheskoy svyaznoati) SSSRI PERIODICAL: Doklady Akademii NaW191957,vol-117,Nr 5,pp.755-758 (Uz7;SR) ABSTRACT: The author continues the investigation of the spaces of sym- metric almost symplectic connection previously considered by himself [Ref.1]. For their tensor of curvature B a R".'~4 he Sives the properties Ij - B:Lj,kl + Dji,kl = 0 (2) Bi.j,kl + Bjk,il + Bki,jl 0 (3) Blj,ik + Bjl,ki + Bki,jl + Bik,lj = 0 etd. Then such spaces of symmetric almost symplectic connection are considered for which the elements of the Lie algebra of the holonomy group, which are associated to the elementary Card 1/3 cycles, belong to the Lie algebra of the symplectic group. The Tensor of Curvature and Some Types of Spaces With Sym- 20-5-7/54 metric Almost Symplectic Connection For these spaces the relation (4) V V. -S 0 is characteristic. This relation is 1 j ki satisfied by the spaces with 0a ij ), a gal,,) __:14k ki ijk = 3 Xk x1 xt 0 and by the spaces with B ij,kl = 0 An example of a further space (different from the two latter special types) for which (4) is satisfied is given. Finally spaces od symmetric almost symplectic connection are considered for which (5) b i a jk T 0 1 2 jki These are spaces with covariantly constant volume k ~det 11 aj det X From (5) it follows that the space is equiaffine bilt not con- versely. If the dimension of the space is 2 or 41 then it fol- Card 2/3 lows from (5) that the space is symmetrically qymplectically The Tbneor of Curvature and Some Types.of Spaces With Sym- 20-5-7/54- metric Almost Symplectic Connection connected. 1 Soviet reference is quoted. ASSOCIATIOUt Municipal Pedagogical Institute imeni V.P. Potemkin,Moscow (Moskovskiy gorodskoy pedagogicheakiy institut imeni V.P. Potemkina) PRESEITTED: By I.G. Petrovskiy, Academician, 11 June 1957 SUBMITTED% 8 June 1957 AVAILABLEs Library of Congress Card 3/3 5W--QA- i LEMM)~~L V G. , Cand Phys-Math Sci (diss) "Bicl4p of symmetrical Mloa,1958. Cover, 3 PP. (Mos City Ped Inst im V.P. Potemk. #.) 100 copies. (KL, 12-58, 96) -10- 16(i) AUTHOR: Lemleyn, V.G. SOV/20-128-4-SI/65 TITLE: Generalization of Invariant Differentiation in a Fractional Linear Group and Splitting of an Affine Connectivity Object PERIODICAL: Doklady Akademii nauk SSSR, 1959,vol 128,Nr 4,pp 672-673 (USSR) ABSTRACT: According to the usual rules the invariant differentiation in the group of broken linear transformations can be carried out for the construction of a covariant differential if instead of the affine connectivity object rp a certain object ik (3) 1 '~ln a 1 p Zin a Jk - (n+1) J Dk - T-a-+ 17 k -~.j is used, where a is a relative scalar with the weight 1. The affine connectivity object r~k can be split into two objects: 1) in ~-~ which introduces the invariant differentiation jk in the fractional linear group and which is determined only by a, Card 1/2 and 2) in the so-called symmetrical combining object Generalization of Invariant Differentiation in a SOV/20-128-4-9/65 Fractional Linear Group and Splitting of an Affine Connectivity Object P Gp = G . which with respect to the invariant differEintiation ik kj p in the fractional linear group plays the same part as r Jk with respect to the ordinary differentiation. ASSOCIATION:Moskovskiy gorodskoy pedagogicheskiy institut imeni V.P. Potemkina (Moscow City Pedagogical Institute imeni V.P. Potemkin) PREESENTEDs June 1, 1959, by P.S.Aleksandrov, Academician SUBMITTED: May 29, 1959 Card 2/2 I (D, 5-6 0 0 66720 AUTHOR: Lemleyn, V.G. SOV/20-129-2-5/6,, TITLE: Local Center-Projective Spaces of a Differentiable Vanifol-_ and the J~ Object Which Defines an Invariant Differan- ik tiation in a Fraction-linear Group PERIODICAL: Doklady Akademii nauk SSSR,1959,vol 129,Nr 2,pp 254-256(USSR) r n~ ABSTRACT: A center-projective space 1P is assumed to be connected with every point M of the n-dimensional differentiable manifold JVnJ, whereby the transformation x il=X it (xi ) of the local coordinate systems of fVn~ implies the transformation ox" i ~xi u Jln det axr' 1 axr 11 ui+1 XT Card 1/3 of the coordinates (u in iP1. Here it is U 66720 SOV20-120-2- -166 Local Center-Projective Spaces of a Differentiable Manifold and the 9,, Object Yrnich Defines an Invariant Differentiation in a Fraction- JK linear Group adet au r' 3det 11 1 11 1xr, aur qxr auk U-0 qxk 1, If on IVnj a relative scalar a=a(xr) with the weight.,one is given, then (see Z_Ref 17) the object tp 1 Sp gin a 1 gp aln a jk (n+ly i qxk + -(-n-+17 k ?xj can be constructed. To every point M of iV'i there exists a transformation r' r xrl- r that (IT)=-O. By a fractional-linear bqxq+1 , -0 f P: k' Card 2/3 transformation therefore a coordinate system can always be 66720 SOV/20-129-2-5/606 Local Center-Projective Spaces of a Differentiable Manifold and the IP Object Which Defines an Invariant Differentiation in a Fraction- ik linear Group found on 11 such that in a given point the invariant differentiation defined by ~~ is identical with the ordinary jk differentiation in the fractional-linear group. There is 1 Soviet reference. ASSOCIATION:Moskovskiy gorodskoy pedagogicheskiy institut imeni V.P. Potemkina (Moscow Municipal Pedagogical Institute imeni V.P.Potemkin) PRESENTED; July 3, 1959, by I.G.Petrovskiy, Academician SUBIMITTED: June 26, 1959 Card 3/3 68794 tff4+ 0 0 SIO 20160113 1 /o 1 /oo 3/c 6o AUTHORt Lemleyn,V.G. TITLEt Induction of Tonstant Curvature Connectivity in Associated Centre-Projective Spaces of a Locally Projactive Manifoldilp PERIODICALs Doklady Lkademii nauk SSSR91960,Vol 131,Nr 1,pp 17-.20 (USSR) ABSTRACTs The author continues his investigations startet in /-Ref 1,2_1. Let a locally -projective manifold be defined by non-degenerate fractional linear transformations of the local coordinate systems I a xi (1) xi a + c bix + 1 and let on it the fundamental relative scalar a a(3:) with weight I be.given ; let (5) det I(R ij(x) 11 ~ 0 The magnitude Card 1 3 68794 Indmotion of Constant Curvature Connectivity in S/020/60/131/01/003/c6o Associated Centre-Projective Spaces of a Locally Projective Manifold only if (10) 06 = c ijuiUJ +c2c iui + 1 By the natural requirement 2 (11) of, , det 1i gii det lie 10i - cij 0 It and the fundamental tensor (gij gji) itself are determined up to the factors 6 (and respectively) which are equal to 2 n-th roots of 1 ; c det 11cic - c I n j ij There are 2 Soviet references. ASSOCIATION: Maskovarkiy gorodskoy pedagogicheskiy institnt imeni V.P.Potem- kins, (Moscow Municipal Pedagogical Institute imeni V.P. Potemkin) PRESENTED: November 19,1959, 6y F.6. Aleksandrov,kcademician SUBMITTED; November 13,1959 Card 3/3 .01391 .102U16011321061101'068 AUTHOR:- Lemleyn, V.G. C111/C222 TITLE: Projective and Projective - Metric Transfers in Manifoldt With Affine Connectivity and in Riemannian Spaces PERIODICAL: Doklady Akademii nauk SSSR,1960,Vol. 132,No. 6,pp. 1261-1264 TEXT: On the differentiable manifold ~ n ~ let be given the object (a.) the components of which are transformed by the coordinate transformation i I x xill"(x') as follows xi a 1 ln det xr/ xr' ai, - i - Tn+ 17 ii xi` Let to every vector of the central affine tangenting space An correspond the. object (1) u -a, + Card 1/4 '11391 Projective and Projective-Yetric Transfers 310201601132106110,1068 in Manifolds With Affine Connectivity and C111/C222 in Riemannian Spaces of the locally central - projective space (Pn (compare CRef. 1)) ; let to n? - n, -tor of the space IB r dual to 'A ~ corresp every covec ond the object (2) U. + a i n n of the space dual to IP The defined correspondences are biunique since the formulas (1), (2) do nbt depend on the choice of the-coordinates n ., in the V and can be written in the form U4 (3) a Ul + 1 (4) u a, PnJ n The object (U 0) defines an invariant point in and in it de_ Card 2/4 ~J!391 Projective and Projective-Metric Transfers S/020/60/132/06/lo./068 in Manifolds With Affine Connectivity and C111/C222 in Riemannian Spaces fines the invariant plane u i u + I - 0 while (uo) in fpn~ defines an o i i invariant plane and in n it defines an invariant point. If on V n~ an affine oonnection (r~k pj ) is given, then J + F 0 describes a parallel transfer of the vector k , lk Substituting for this vector its value (3), then one obtains Uq J f- q q r 1 (10) Dxk UL jk + U u '3xk ai ik This system determines the projective transfers of the local central-pro- jective spaces (,n along a curve on Vn~ Then the author considers the case of a Riemannian connectivity (- P and Card 3/4 ik 81391 Projective and Projective--etric Transfers 3/020/60/132/06/10/068 in 11anifolds With Affine Connectivity and C111/C222 in Riemannian Spaces similar questions. There are 3 Soviet references. ASSOCIATION: Moskovekiy gorodskoy pedagogicheskiy institut imeni V.P. Potemkina (Hoscow Municipal Pedagogical Institute imeni V.P. Potemkin) PRE,SENTED& March 2, 196o, by P.S. Aleksandrov, Academician SUBMITTED: March 1, 1960 Card 4/4 Y6 AW031XX 61020160113310061 0 C 111/ C 333 AUTHORs L 1% ---1-9~.- yn,-V-~-G"' TITLEs On the Geometric Meaning of the Projective Curvature Tensor in Manifolds With Affine Connectivity PERIODICAL: Doklady Akademii nauk SSSR, 196o, vol. 133, No. 6, pp. 1287--1290 TEXTs Let an object of affine connection r Pk = F-Fkj ) be given on the differentiable manifold ~Vn I . Then in every local cen-bro- Projective space t Pn I (see (Ref.4.)) there arises the invariant hyperquadric (see (Ref. 5)) a. (,) F , W - 6'il W Uiui (1) )2 al bi (n+1 2 r ai (x) ni + I = 0 Tn-+ 17 a where G'-j(x) is the symmetric part of the Ricci tensor. / 1J Card 1 5 863,72 S/020 bUI13310061021103!XX C 1k C 333 Dn the Geometric Meaning of the Projective Curvature Tensor in Manifolds With Affine Connectivity Every ~ PnI can be considered as a symmetric projective-Euclidean space (see (Ref.3)) and, if it is moreover det as a space of constant curvature. The connection F P (x,u) can be defined by polar correlative jk rel-ation with respect to (1). Let P h. ji(x) = Rh - 2 P (X) n + 2 ~h P (x), k k,ii(x) ijJ k where P ii (X) 12' (n+1) R ji + Vji and V3.j is the equialIne (1-n ) tensor, the tensor of the projective curvature of the initial space of affine connection. Let Card 2/ 5 863,77-- S/020/60/133/006/021/031XX C 1-11/ C 333 On the Geometric Meaning of the Projective Curvature Tensor in Manifolds With Affine Connectivity (6 ) h h h]. Qk,ji(x) 2 0 V ik)(x) - Vjx (x) k It is stated that then it holds (7) Ph k,ji (x) _ Qh k,ji(x) = Rhk,ji(x) - rhk,ii (XIO), where (4) rh Sh ~h k,ji (xIO) (1 n) ik (x) - 1 GJk(x)' 1-n i j rh, ji(x~u) is the curvature tensor in k ~ Pn Theorems The difference of the tensor of projective curvature and the tensor (6) which only depends on the equiaffinity tensor is, in every point of the considered manifold, equal to the difference: of the curvature ten8or of the original affine connection and of Card 315 --_36372 S/020/60/133/006/021/031XX 0 Ill/ 0 333 On the Geometric Meaning of the Projective Curvature Tensor in Manifold3 With Affine Connectivity the curvature tensor of the local space which is calculated in the corresponding point. The author investigates several spacial cases. In the case of equiaffine projective-Euclidean spaces under nondegenerate Ricci tensor of the original affine connection the author introduces a scalar magnitude K(x) so that the local spaces are transformed in.to spaces of constant curvature K(x) with a special metric tensor. The author refers to the possibility of expressing the tensors Phk,ji (x) and Qhk, ji(x) by the components of the connecting object (see (Ref.7)) and their first derivatives. There are 7 references& 6 Soviet and 1 Dutch. EAbstractor's note. (Ref.3) is a paper of P. A. Shirokov in Tr. seminars, po vekt. i tenzoru. analizu, v.8.,1950. (Ref-4) is a Card 4/5 8637Z B10201601133100610211031XX C Ill/ C 333 On the Geometric Meaning of the Projective Curvature Tensor in Manifolds With Affine Connectivity I paper of the author in Doklady Akademii nauk SSSR, 1959, Vol- 12!), No. 2. (Ref-5) is a paper of the author in Boklady Akademii nauk sssR, ig6o, Vol. 132, No. 6. (Ref. 6) is a paper of the author in Doklady Akademii nauk SSSR, 1960, Vol. 131, No. 1. (Ref-7) is a paper of the author in Doklady Akademii nauk SSSR, 1959, Vol. 1213Y No. 4.3 ASSOCIATION8 Moskovskiy gorodskoy pedagogicheskiy Institut imeni V. P. Potemkina (Moscow Municipal Pedagogical Institute imeni~ V. P. Potemkin) PRESENTEDt April 13,~ 1960., by P. S. Aleksandrov, Academician SUBMITTEDi April 20, 1960 Card 5/5 LEMLEYN, V,rr,., Spaces with conter-projective connectivity (fvj ix 2.r,14- -aa mmilfolds immersed in the space of representation of an extended pseudogroup of analytical transformations, DALMI SSSR 138 no,6:1291-12% Je 161, (MIRk 14:6) 1. Moskovskiy gosudarstvennyy pedagogicheskiy institut im. V.I. Lenina. Predstavleno akademikom. P.S.Aleksanrovym. (Geometry, Projective) LRE-EYN, V.G. One prooerty of alternative (pasi-groups ,ti'.h an measure. Do',"!. AN SSSR 164 no-4:74C-742 0 (MTHA 18.10) 1. Mosko-,rskiy gosudarstvennyy pedagogicheskly irist'itut ini, 11.1. Lenina. Sulnittued March 4, 1965- LEI 11211, Krystyna Use of the resin "Araldit" in repairing of experimental mandibular fractures in the rabbit. Roczn. pom. akad. med. Swierczewski 11: 399-410 165. 1. Z Kliniki Chirurgii Stomatologicznej Pomorskiej Akademi-i Medycznej Werownik: P.7of. dr. I. Semadeni-Konopacka). i~rystyna ContribuLion to the use of reging in the 'r-reat.-nent ~;f .J ~ fr&cture5. Czas. Stomat. 18 no.8/9;1171-1172 Ag-S 1,`5 1. Z Kliniki Chlrurgii SLoTtF-tolorjczne-' Pom-orskie.- A14 w S:7czo~-;nLe .3 (Kiem,inik: prcf'. dr. med. 1. LE-21,1ERW, rE. K. (Engineer) AID P-3 Subject uSSRA;ngineering Card 1/1 Author Lemmerman, Ye. K., Engineer Title Economical type of light weight walls made of light weight concrete blocks Periodical Sbor. mat. o nov. tekh. v stroi. 2, 8 - 11, 1954 Abstract The author describes'his new method (adopted by one of the Trusts of the Building Ministry) of erecting light weight hollow walls consisting of two thin walls made of ,15.35" wide concrete blocks connected at 20.47n or 36.4 intervals with the same concrete blocks placed sidewards. In corner connections some reinforcing bars are used. The article is illustrated with 6 graphs. Institutions: Not given Submitted No date IMMYN, G.A., professor. My recollections of the Department of Ph.Vaics At Darkov University and of my work there from 1902 to 1906. Uch.sap.KHGU 60:51-55 '55. NUU 10:1) (Kharkov UnivAxzIty--Histor7) (Physical laboratories) ,. ' 11 "A- 'W-w- -11, -I-iii~ -~ ~F I -IL, t - Mald -t9, M-1-t-MV4 - -1 M~- LEWTE, M.; TEPAC, I. (Bucuresti) The absolute age of the earth. Naturs, Geografie 16 no, 2: 30-37 Mr-Ap 164. ACC NRt -AT5D29607 SOURCE CODE: RU/0024/65/000/005/0035/0()40; (Geologist; Bucharest) AUTHOR: Lemne, M. (Geologist; Bucharest); T~p ORG: none TITLE: Radioactivity and terrestrial heat SOURCE: Natura. Seria geografie-geologie, no. 5, 1965, 35-40 TOPIC TAGS: radioactivity effect, earth radiation, earth thermodynamics, solar radiation ABSTRACT: The authors combine arguments from the technical literature of many countries to support their conclusion th&t rac!4cactivity is a principal source of terrestrial heatVThe argument is bas(,~ on th;--e points: heat from the sun is not felt at depths beyond 20 meters; heat fror.,. the intei--r of the earth (if its origin was as a part detached from -the sun) should have 'tcen exhausted after about 40 million years, while current estimates of the earth's age are much higher -than this; and there exist huge quantities of widely distri*.- ed radioactive substances in the interior of the earth. Orig. art. has: 3 --bles. [Based on aLthors' Eng. abst.] IJPRS: 33,5421 SUB CODE.- 08, 0-3 SUBM DATE: none SOV REF: 004 (YIH REF: 004 -Card JA ID7 BOFOESM, N.; CRL'A,, G. ; COJERFANU, F.; 1EMNEAllu ll~ Eyperimental studies on the charac-ler.f5tics of pc~~e-. in the sinale sealt. vallve. with diffaser. Ful St si Tchn Tim 0 8 no.1:95-10-' Ja-Je 163. CRETA, G.; LEMANU, N.; FARGAS, D. U Calculation of steam transformations by electronic digital COMPUters. Studii tehn Timisoara 10 no.2:355-365 Jl-D 163. Teodor,__in,-.; U1,111EA, Sxabin, ing.; 'j ~ -1 fir Mechanized caravans for loadinr, bu k arid sea~,onal gocds. i_. ev ca 4 fer 13 no.1:14-.18 ja 165. LEMNIJP I. Some data on the U,S.S.,R.. Industry. Problems econ 18 no,3:122- 125 Mr 165. BURSMN, I.; LEMI&,,L ~111. ~ Economic development of the socialist countries in 1962 in figures. Probleme econ 16 no~.6:78-89 Je 163. LEMNIJ, I. Changes in the structure of Rumanian industrial production. Frob-1--me econ 16 no.1:16-28 Ja 163. BURSTEIN,, I.;_LEMJ, 1~- SPIRIDON, A, The economy of socialist countries in fun development. Probleme econ 15 no.7:74-88 JI 162. % LEMNIJ, I.; FUIU, " Aspects of the postwar international economic cooperation. Problems econ 17 no.3:88-101 Mr 164. LEMPAP Henryk Cytologic test in diagnosis of the loss of the amniotic fluid. Polski tygod. lek. 16 no.22:824-825 29 My 161. 1. Z II Kliniki Poloznictwa i Chorob kobiecych Sl. A.M. v Bytomiu; kierowniks. prof: dr med. Bronislaw Stepowski. (AMNIOTIC FLUID) (PREGNANCY compl) .v, inzb; KACPRZAKj Kazimierz,, Inz,; ORLINSKI, Henry'k. mgr; -"MUarakgQa~ CMCKI, Jan, inz.; WARCIIAL, Boguslaw, mgr inz.; WOTCIECHOWSIKI, Jacekp mgr inz, Analysis of the utilization of supporting pillars with coner3te stowing. Rudy i metale 6 no.9:389-394 S 161. YBVDOKIMOV, V.; BAKABOV, P.; LEMPERT, A. ' 0 Horizontal vacuum kettle for rendering fat in the NProgresism Factory. Mias.ind.SSSR 27 no.1:23 156. NLRA 9:6) (Oils and fats) (Vacuum apparatus) l,'R-'PERTI B.L.; LEYTES, F.-I. Role of the reduct~cn wP t~--i A,~v,'Yt-!: a,-tiv,ty of the acyrtl- wall in the pathogene5.s of 1-im,"A inf -11tratic'n. Biul. eksp. biol. i med. 55 / i.e. c6/ r,~). r-,- I- 29 e?63 (MIFIA 1:7:8) 1. Iz kafedry patulcgicheskr-y f-Ilziologii za-v. - prof. %M.Leytes) TSentrallnogo instituta vrac~ey i TSeritralv- nogo instituta kurortlclogii t f.izioterapiL ( dir. G.N. 'redstavle-na deystviteitnym chlenora -Q-UJ S3'R V.Kh.VasJIarI-r-,. .r ej - LEMPA, Henryk Use of Crystallization of the amniotic fluid for diagnostic puarposes. Ginek. pol. 33 no.5:643-652 162. l. Z II Kliniki Poloznictwa i Chorob Kobiecych Slaskiej M.Kierownik: prof. dr med. B. Stepowski. (A1,94IOTIC FLUID) LEMPERT, A.E.,-- in.zh. '62. Modernization of belt dryers. Khim.mash. no.2:37-28 Mr (MIRA 15:3) (Drying apparatus) LEYTES., F. L..,'kand. med. nauk; LEMPERT, B. L.; VIYUROVA, Z. D. Case of aortic aneurysm in Marfan's syndrome. Terap. 324 no.~J: 106-109 162. O~M 15: 7) 1. Iz Maskovskoy rogodskoy bollnitsy No. 56 (glavnyy vrach - dotsent Ye. Ya. Khesin) (ARACHNODACTYLY) (AORTIC ANEURYSMS) SUKASOVA, M.T.- NIATOVA, Ye.Ye.; LEMPERT, B.L. Effect of da-'Iipinj~ on the development of expe-rim-ental athercsclerosis in rabbits. Yardiologiia 4 no.6242-48 t~-D 164. (KI-RA 18:8) 1. Institut terapit (direktor -- prof. A.L.Myasnikov) AMN SSSR, Moskva. LKYTES, F.L.; UEMPERT, B.L* Localization of lipoproteinic lipase in some tissues of white rats. Dakl. AN SSVOR 157 no.3:672-673 Jl 164. (MIRA 17:7) 1. TSentrallw institut usovershenstvovaniya vrachey i TSen- trallnrl institut kurortologii I fizioterapii, ProdBtdvleno akademi:km A,N. Bakulevym. a LEYTFS, F.L., prof.; LEMPERT, B.L. Histoc';.'Iemi-cal method for the detection of lipoproll-ein lipase enzyme. Biul. eksp. biol. i med. 60 no.7:123-125 Jl 165. (MIRA 18:8) 1. Kafedra patologicheskoy fiziologil (zav.- prof. S.M. Leytes) TSentrallnogo instituta usovershenstvovaniya vrachey i TSentrall- nyy institut kurortologil i fizioterapii (direktor - kand. med. nauk G.N. Pospelova), Mosk~ia. LEICP','RT B T Effa,!L of !itreBa and Jts comb-Ination wish rholesterr" ~~r content of P-lipoprotelina J.n thp aorlic wall in Pr~,bl, en~~ok, i gorn. 11 no-5:74-77 S-0 165~ P A 19 ; I Kafedra patologichaskoy fiziologli (zav, - prof~ TSentrallnogo instituta usovershenst,,rovaniya vrach-.--.-,z, Mookva. Submil.ted October 24, 1964. VANWSKIY, A., inshener; LMG4MT, X., inshoner. Automatic apparatus for measuring amounts of voter and salt in dough viaking. Mias.ind.SSSR 26 ne.6:5-8 '55m (MlaA 9:2) l.Lanivigradskiy mys,sokembinate (Dan&) (Measuring instranents) LENFERT E - BUROVA, 0. Bringing of hides and skins in a worm apparatus. Rias.ind.SSSR 33 no.5:21-23 162. 041-RA 15:12) 1. Leningradskiy myasokombinat. (Hides and skins) (Brining) IZIPERT, G. L. LaTERT, G. L. -- "On the Problem of Methods of Quantitative Characterization of the Direction of the Electrical Axis of the Heart." Academy of Medical Science USSR. Joint Council of the Group of Leningrad Institutes, Leningrad 1955. (Dissertation for the Degree of Candidate in Medical SciencesJ So; Knizbaya Letopis' No 31 1956 LEMPART, G.L. Differentiation of the associated effect of two factors on the direction of electrical cardiac axis. Terap. arkh. 27 no.8:87-91 155 (MLRA 9:5) 1.Zav. elektrokardiograficheakim kabinetom poliklinichookogo otdolonlys. 1-y Rizhakoy, gorodskoy klinicheokoy bolluitsy. (RUCTROCARDIOGRAPHY, -differentiation of associated off. of 2 factors on direction of cardiac axis.) LIKPIMT, G.L. "Zlectrocardiography.0 G.IA. Dekhtiarl. Reviewed by G.L.Iampert. Terap.arkh. 28 no.5:83-85 156. (MLRA 9:10) (ELMCTROGARDIOGRAPHT) (DMTIARI, G.IA.) LSSR / Human and Animal Physiology. Blood Circulation. TJL Abs Jour :Ref Zhur - BiolQgiya, No 1, 1959, No- 3369 Author :,,lempert, G. L. Inst : First-Rig"A _'C1't.Y'Hospital Title :Perrtaining to Methods of Measuxing ECG Waves Orig Pub :Tr. 1-y Rizhsk. gor. klinich. bollnitay. Riga, 1957, 51-58 Abstract : When measuring the height of the waves from the so- called isoelectric line, the thickness of this line, which varies from 0-5 - 3 mm, is not taken into consid- eration. Depending on whether the waves are measured from the upper or lower border or from the middle of the iaoeloctric line, a considerable difference in the size of the waves and of the angle "alpha" may be noted. It is rec nded that the positive waves of the ECG be measured from the upper border and the negative waves Card 1/2 26 . . TISSR / Human and Animal Physiology. Blood Circulation. T-4 Abe Jour : Ref Zhur - Biologiya, No 1, 1959, No- 3369 from the lower border of the isoolectric line. Such a method of measuring the sizes of the ECG-Yaves will ensure a most correct determination of the direction of the electrical axis of the heart. Card 2/2 WsR / Human and Animal Physiology. Blood Circulation. T-4 AbB Jour :'Ref Zhur - Biologiya, No 1, 1959, No. 3370 Author 4_ja~La~rt, G. L - Inst Fir-a-Mg-a-My"Tospital Title About a Method for Determination of the Angle "Alpha" of the Electrocardiagram Orig Pub Tr. 1-y Rizhak. gor. klinich. boltnitsy. Riga, 1957, 59-62 Abstract The size of the angle "Alpha" can be conveniently determined from tables on which Its values are shown correlated to the values of the ECG waves In the leads I and III. The accuracy of the findings, however, de- creases as the absolute sizes of the ECG waves diminish. A diagram of a perfected device to given, by which the angle "Alpha" can be determined in the process of a synchronous determination of the values of the BCG Card 1/2 27 LEMPART, G.L. (Riga) r ft"I",-~--, uFrinciples and atlas electrocardiograpby' [in Geimmanj by R.7-uckjqr- man.n. Reviewed by G.L.lempert. Terap.arkh. 30 no.1:81-83 is 1,98. (UNGTROUARDIOGRAPHY) (MMA 11:3) i4g~q,Grigoriy Leonidovich; PISIIMIINYY, R.Ya., red.I;PARAIMNA, N.L.,..tekhn. red. (Fundamentals of electrocardiology] Osnovy elektrokardio- logii. Moskia, Medgiz, 1963. 326 p. .(MIRA'17:2) - -)A-, - , : -ill Illillemll fit avilt iw - 331.New componnik %v ill 1). Behe, 1"~. IxIII)WIA Ittill. I,. Gvertild.. (.11agyar Or"I -7 Ul- "'t, I ~) --)'2 - -N 0. 1 ato' pp. 31'2, Val 01, 1951, No; 4, till, 117-A-51 a lalls.i is I'lloxyll mailkly ~ fraill tilt, invesli"'Ition's, I out, by DAgreit anit colhihiii-alors Ilial. 1.1w . tmilidt.s. tollilditivs. vic'(1hex -locnint, 'aliryliv valluthie lunt alinsilletic prollaties'. In order to estnblkll file whilimis beLwvell tilt, al st.1-111-1111v aliti. I tic local almehilletic activitv Chunk Aituted halo -it of thew nticlear sule, it compmuds wav prepawd, Tile, divibylglycyl halo- gwilo 'milkles and tolitiditics prepareti. from (lie Carrospollding chloroudyl derivatives show local aaacstlielie activity. anct several compounds even Surptiss Novocaine ill th-is rcspecl. ; their toxicity m Jov, but strop-r. local irritating propertics prohibit. their pract.iwl iffie.,Thuw. irrilatin propertIes moy 9 'It lie Ilimillished !11141 si Ill ull'.% neously 1.11c Aliologic. -c -ed by thu intro- autivity 91 Bit. compound hici at, ductioll of a second five aromatic amint) group! I lowevev, tile tillis Obtailled derivatives tire. highly toxiv. This toxicity C11111 Aic dimillisliLd by tile acylatioll (neetylation or succinylatioff) or tile ~Secoll 111111110 grin d' mp but tbeir retittetA thereby, The C "y lllyl~ vp- 11 a "miti I"! I illn lmillllk~. Ill ared 11 4 villre it is Witter Soluble. structilre -and tim It pCoved to It(,, It more polctil. local atme-Altelle tima. Novornine in spite of its ["t, (more precisely, lonixed) carboxyl groult. Sewral'quatermary deri- Itives of tile fullounds mentiolled 11bove 1VVrV and Inw, tcd in res -ma. prepartid. Aigi, spvct in their p1ml it tumc-atlictic activity of ;Cologivat value, Tile loc. tile ilkyl quilterflary Coll) poltill Is Is low, tile -.10MLY of the Mlylic qttaternary compounds w, ,i found to 1- of the same. order Its Unit of tile tertiary ~mlts. Out to their low Solubility in water tile biologiall activity ;of tile henzylic (III.Acrouy-cou-4)O[Inds Wils'not eq itivestigated. In r pVet 10 jile Qffc,~J,df j;t%C litteleAr HIII)stituents on tile loral mnkest;A~W.ic pqteney of Im. dx,;iWl1 that tilm ~01nPOUnIlS Jl;C A3,4 4tc, ric - "ojw assumed -by I.Ufhfrcii not only tile . vs -ible for tile Ond collaborators to solely. I spons harmamlogic. activity - but the dectron affinity of tile SubstitticnL" IN Also of decisive imptrUAnce. L F- Jtz-=. Dingary/Organic Chemistry Synthetic Organic Chemistry: E-2 Abst Joux-nal: Referat Zhur - Khimiya, 110 19, 1956, 611L97 Author-. Beke, D., ~ ~pert~,K., Gyermek, L. Institution: None Title: New Local Anesthetic Agents Original Periodical: Neue Lokalanaesthetisch wirksame Verbindungen; Acta chim. Acad. sci., hung., 1954, 5, No 1-2, 143-149; German; Russian and D3glish restm6 Abstract: There have been prepared a number of N-diethylglycylanilides ArNHCOCH2N(C2H )2 (GA) containing various halogen and alkyl sub- stituents in t~; aromatic nucleus and the local anesthetic rproper- ties of the-hydrochlorides an4 acid succinates AS) of these com- pounds have been investigated. On treatment of ArNH2ClCH CGCl there are obtained ArNHCOC`H2C1 (CA) with a yiel$ of 70-9~ which give with HN(C2H .5)2 the GA with a yield of 60-76%. The following CA and GA have been prepared (listed are: Ar, MP 0 C, of CA, and Card 1/3 Hungary/organic chemistry - Synthetic Organic Chemistry, E-2 Abst Journal: Referat Zhur - Khimiya, No 19, 1956, 614,97 Abstract: MP 0 C of hydrochloride of GA); o-chlor..~iphenYl, 74-75, 108-111; ni-ch-lorophenyl, 100-101~ 219-221; p-chlorophemyl, 168~ 178-179; 2,4-di-ehlorophenyl, 117-118, 172-173; 2,5-dichloxrophehyl, 115-114-* 172-173; 2,6aWchlorophenyl, 172-173, 168-169., AS., MPL-130-1320; 3,5-dichlorophenyl, 141-14-2, W6-2o7; 2,4,6-ti-ichlorophenyl, 181, 218-220; p-bromophenyl, 176-177, 167-168; 2-br=-6-chlorophanyl, 167-17o, 175-181; 2.5-dibromophenyl, 136-138, 188-190; 2,6- dibromrhenyl, 170, 195, AS, 132-134; 2,4,6-tribrcmophenyl, 217-218, 211-2113; 4-chlor-o-tolyl, 128-129, 120-121; 4,6-dichlor-o-tolyl, 177-178, 177.5, AS 102-103; 4-brom-o-tolyl, 132-134, 152-15~; 4,6- dibrom-o-tolyl, 196-197, 135-137, AS 100-102; 2,6-dichlor-i,tolyl, 167-169, 193-195; 2-brom-p-tolyi, 118-119, 146-147; 2,6-dil5rom-p- tolyl, 188-190, 18.87190, AS 138-140; phenyl, 134-135, 108-10* o-tolyl, 112, 1.*~9-120;-p-tolyl, 163-164,-147-148; o-etbylphen~l, lo2-lo4, l38-l4CF;6t-naPhthYl, 159-1*, 162-163; 2-methylnaphthyl-l,- 167-168, 210-211; about'l/2 of syntlMsized GGA have local anesthetic properties approximatizig those of novocaln. Substitug"Mts in ortho- and orthol-positic;ns are not indispensible for high anesthetic ac- tivity, thus GA (Ar = 3,5-dichlIrophenyl) �s as act:Lve as the Card 2/3 Hungary/Organic Chemistry - Synthetic Organic Chemistx7, E-2 Abs!t Journal: Referat Zhur - Khimiya, No 19, 1956, 61497 Abstract: 2,6-isomer and exceeds that of novocain, while GA (Ar = 4-chlor.-o- tolyl) is 1.4 times as active as novocain. Card 3/3 -IJ N New I" UmAMUm IL 1). W-r, F- Lmpert, asil I- GYvrinck 1954 4 H40!7Mt titmituteAdi, tby-"-YIx Shows Oat, within Oiii d4-,s cA c01'ljpn~inds, the intr'4uctiln ir't'-, the mol. of a further val)stitticnt (11aWgen, alkyl, Nu'. Nil, aLylawide group) into tlic free oxibc position (with m ct to the -PC diudzylglycylamid,, grocip) immiscs tite anx5thetic activity lrrtw~i- eel Vt., El u[ the Occtrost affinity of the new siib-Aituent. WWI_ f ar urs therefore appear important. It We snivits mibstituents are t ititrvAnced into tht: frci: para position of the 2 -. 6Ailialcacnodiethyl- glycYlanifide, their eff,,ci; on the. biological. artivity of the prodtict dcpendsontlicirelt-etrL)nafiijxit), Th;7prep, is dmcribcd of a series of 2 ! U-dichloro- or -dibrnma-4-acetamidoariffldes wltl~ an XI- dicthylglycyl Q-~raup- The dihalageno-4-nitroanifiria is treatvd With ClIXI-COCI, ind the pmduct with NHEt, to give the ;%W whi i r n ch 5 cdaced a d acylated to the Quaternary deriv. of the la-,t-namcd are prepared. Fwinuhe and ~,f ci~l.~arupounds are given. P~ ",Illy - ~111 kle_ .7. New cinvouads With local Aflaesthetle activity, IV. K Le y e r in e I,. Magyar 161hdai Folyd- 55, 14o. 7, pp. 193-7195 Aiialogucsof pound of local anitestlictle activity,--, were prepured ljy introducing,other heterocyclic systems into the molecule. (1), By reactio o-plienylenediamine with itionochlar 1. acetic acid an dictitylanifne 2-4fictbyl-ambio-meth~ littizimidazole wus obtained.which was converted to its crystalline dlcliloroh~dratc (in. p. 200 to 211 1C) by, tlj~ ctllylacetate-Ity(Itochtorte,acid-etlit:r method, (2) Th~ condoisationof N,NI-diethyl-glyciiionitriltiwitlia-atnhio- thloplienol yielAs directly 2-diethylarnino-nitthylbenz thfaiale. This compound wlis obtained fit better yields bTtthe Interaction of o,6'-diaiiiint)-(Iipheiiyl.dlsitipblele w It chloroacetyl chloride and diethylatnine through the Intermediates 2,2'-di-(cliloroicetaiiiiiio)-dipheiiyI tW Sulphide and. 2,2'-di-(dfetltylgly-e~laiiiiiio)-dipliett)-I di- stilphide by reductive cyclizatiom The nionochlor- iydrate.of this compound yleld~ hy,roscopic white ieedles, melting at 132-133 *C. (13) 'IC bromination A.- of quinaldine with bromosuccininxide y1elds 2-bronto- intAbyl quinnihic which was reacted with diethylasaine In obtain 2-dicthylaminoinethyl (juhioline. 16- diehloro. hydrae, it ixiwder, melted at .207 *C. - Accordh to the inations three prelinfluary pharmacological exam mically "illbstitiltell heterrWyclic C01111musida Mimed lfwal annesthetle activity at least equal to tWit of novO -dicthylambir) nethyl C11111C. Moreover the rompoin)(I 2 1 "juhioline exhlbited mitih[staminic and antladrenergic activity. J UMERT, Ka~oly; BREUER, Judit; IZ14PLRT KAROLYNE SRETER, M" Hydantoins, _#iohydantoins, glycocyamidines. Ft. 3. I-lagy kem folyoir 65 no.4:142-145 Ap 354. 1. Magyar Tudomanyos Aka4emia Kiserleti Orvostudom&nyi Kutato Intezete Korelettani Osztalya., Budapest as Eotvos Lorand Tudomanyegyetem,Szerves-Kami&i Intezet, Budapest. HUNGARY / Organic Chemistry. Organic Synthesis. G-2 Abs Jour: Ref Zhur-Khimiya, No 1, 1959, 1233. Author :Le% .;jpXt4 K., Beke, D., Borovansky, Inst :-, 50-t givelf-. - Title Research in the Field of Local Anesthetics. VI. The Preparation of 4-Amino-3,5-Dichlorothioplienols and Its Certain 5-Alkyl Derivatives. Orig Pub: Magyar kem. folyoirat, 1956, 62, No 11-12, 373-377. kbstract: Starting from 2,6-Cl2C6H NH (I) or N-acetyl.-l M), the 2,6-Cl2-4-HSC6H2NHR Mfi were synthesized via 2,6-C12-4-SO2C1C6H2NHR (IV). By the action of CH2N2 or RII on II, the corresponding 2,6-Cl2-4-- RIS06112BH R (V) are prepared. 14.1 grams of II was heated with 32 milliters of HS03C1 for two Card 1/5 HUNGARY / organic Chemistry. organic Synthesis. G-2, k,bs Jour: Ref Zhur-Khimiya, No 1, 1959, 1233. Abstract: hours at 125-1300C. and after being cooled, IV was obtained (R = H) (IVra), in a 60-65% yield, m. P. 130-1320C. (from C6H6Cl); 10.42 grams of IV-a was fused with 34 grams of ClCH2COOH and 4.6 milliliters of ClCH2COC1 and after it has been heated at 110-1200C. for one hour was poured into 400 milliliters of water. Thus IV obtained (R = COCH2Cl) (IV-b) in a 91-96% yield, m. p. 194-1940C. (from benzene-chloroform); IV (R = COCH3) (IV-c), yield 86%, does not melt up to 3000C., was prepared upon boiling for 15 minutes of 5.2 grams of IV-a with 20 milliliters of glacial acetic acid and 2.1 milliliters of acetic anhydride. A solution of 2.6 grams of IV-a and 13.4 grams of SnC12.2H20 in 55 milliliters of glacial acetic Card 2/5 12 HUNGARY / Organic Chemistry. Organic Synthesis. G-2 Abs Jour: Ref Zhur"Khimiya, No 1, 1959, 1233. Abstract: acid (saturated with HC1 gas), is agitated for 1.5 hours at 200C. and for one hour at 650C. and is filtered. From the filtrate after the addi- tion of 25%o HCl, III was obtained after -,-) 48 hours (R = H) , yield 205/a, m. p. 74-r,160C. III-a was also obtained in a 817o yield by reduc- ing IV-b or IV-o with zinc dust. To 3.25 grams of III in 60 milliliters of ether in the cold was added an ether solution of 2.54 grams of CHP2, "-, 24 hours after being treated with HC1 (acid V was obtained (R = H, RI = CH3), (V-a), yield 89%; V-a was also prepared by methylation with methyl iodide in a 61% yield, m. p. 59-610C. (from benzenei. In the same way other V (R ;= H) were prepared. Given are R1, yield in %, m. p. in OC.: C2H21 78.2, -; C3H7, 65.1, 41-43; C,,Hcj, Card 3/5 HUNGARY / Organic Chemistry. Organic Synthesis. G-2 Abs Jour: Ref Zhur-Khimiya, No 1, 1959, 1233. Abstract: 62/4, -. Upon melting 4.3 grams of V (R 2 1-1, RI = 02H5), with 8.2 grams of C1CH2CO0H and 21.2 milliliters of UCH2001 followed by heating for one hour at 110-1200C.) V was prepared (R = COC112C1, RI = C2H~), yield 94.1%, m. p. 164-160C.; the other V were prepared in the same way (R = COCH2Cl)Zg-iven are RI and m. p. in OC. (from al- .coholff: CH3, 180-160.5; n-C3H7, 168-168.5; n-U,4,Hq, 148-149. All V (R = H) can serve as starting mat- erials for synthesizing compounds with local an- esthetic properties. From 24.3 grams of 3,5-012- 0 H SOP.I'M2 (VI), 85 grams of ClCH COOE and 4-NH2 6 2 , 2 12 milliliters of ClCH2COC1 one obtains (110-1200C., 2 hours) 29.5 grams of 3,5-ClZ-4-ClCH2C0NHC6H2S02- NH2 (VII), m. p. 226-2280C. (from 30% aqueous al- Card 4/5 13 C R T JZ STARK, Firvin, az orvostudomanyok kandidatusa; LMUMT, Yaroly; VAGI, Oszknrne 1.1'---':-.~~--'- :- -* Isolation of benzoic acid from the urine of patients suffering from hyperfunction of the pituitary and adrenal cortex. Magy. Tudom. Akad. Biol. Orv. Oazt. Kozl. 8 no.4:4154'16 1957. 1. Az MTA Kiserleti Orvostudomanyi Kutato Intezet Korelettani Osztalya es a Budapesti Orvostudomanyi Egyetem I. sz. Belklinikaja. (GUSHING SYNIROME, urine in benzoic acid isolation (Hun)) (AIRWAL CORTMC, dis. hyperfunct., isolation of benzoic acid from in-ine (Hun)) (BFMOAT3S, in urine in adrenal cortex hyperfunct. & Gushing synd., isolation of benzoic acid (Hun)) -'~ - --!::: ~, I L T , In. Studies on oc.-I aneztl-etics. V. 4-alkoxy deriv;:tives cf (N. A 1) -2.6-dichiorcamilide hydrochloride. F.9C GiCTA i in Gex~[,an EunE.-ry SC: 1-ionth-lY inAer c-' E'l t EuroT~e-,m Accezsi ns I-C. Vol. 7, No. -3 Narch l'-.58 -- 1 7~ 7 MMAW/Orpnic Chemistry. Synthetic Organic Chemistry. G Abs Jour: Ref. Zhur-Khimiya, No 19, 1958, 6449o. Author Tempert Kardy, Lempert, Karolyne Inst Title Synthetic Materials With Hypotensive Activity. I. Orig Pub: Magyar kem. folyoirat, 1957, 63, No 2-3, 84-87. Abstract: With the intention of studying the relation of hypo- tensive activity to structure, a series of derivatives of 6.,7-dimetboxy-1 2,3,4-tb#ahydroizoquinoline (I) vere synthesized. N-(9 -acetoxybutyl).(I) (Ia) can be derived from (I) and 6 -bromobutylacetate in the presence of C4HS_)3N in an acetone solution, yield 69%, m.p. 61-620 in benzene-ether, hydrochloride, M.P. 171-172~'Jn methyl.. ~ ethyl ketone (M),7, succinate, m.p. 90-92e' (in CC14-ether), Card 1/4 HUNGARY/Organic Chemistry. Synthetic Organic Chemistry. G Abs Jour: Ref. Zhur-Khimiya, No 19, 1958, 6449o. anisoyloxyethyl)4I), can be produced m.p. 177-179'0, and,N-(bcta-veratroyloxyethyl, m.p. 182-184' (both in dhloro-LOorm-ether), and N-( ~ -31,4,,5'-trimethoxybenzoyl- oxybutyl)-(I)) m.p. of hydrochloride 167-1690- Upon the boiling of a solution of (I) with ethylene-chlorhydrin in the.presence of (C~K5~3N and sodium iodide in acetone, N;(6 -oxyethyl)-(I) is produced; yield of hydrochloride 5 -58epl, m.p. 192-1930 (in chloroform-ether). In order to make comparisons in pharmacological methods by the technique of Smorgonskov-Goldfarb (j. gen. chem 194o, 10, 1113), the hydrochlorides of ((S -oxybutyl)- ( - acetoxybutyl)- and ( ~ -3,4,5 trimethoxybenzoyloxy)- diethylamines) m.p. 88-90, 91-93 and 136-138, respective- ly,'were synthesized. The majority of the above compounds Card 3/4 d-3 -try ilung, 59 C, re t r and Lempe r t K Lemper t -S Hun-garian Academy of Sciences On the Bare-Irduced Cleavage of Functional Derivativc-E of p-Tosyl~rlycLae PUB. Acta Cilim A~:ad, Sci Hfun-1, 17, irlo 4, 4?1-47", (195r Hf,,atinZ of p-touyi,~-lyc~nf-, (1) and of its amide ' 11) to 220-230" -nith 14~1~ , di- and triethylamine, leads to the cLeavage of I and II and to the lormation of p-tbiocresol or of the correapond- ing sulfida8 and dislilfides, amine,5, aldehydes, and C;02 . The auovc reactior takes place wlien the f uric tion,01y modified, carboxyl group Contains readily irinizable "Ialuilel hydroFer. The ethy! ester of I on heating with Ni3 at fir-st gives IT whi-ch eub6equently cleave5 as described abuve. C A 11 D1/2 140- LEMBT, Karo Some problems of the relationahip of chemical structure and phar.- macolog,ical effects. CFrv. hatil. 99 no-36:1229-1237 7 Sept 513. 1. A Magyar Tudomanyos Akadenia, Kis'erleti- Orvostudomanyi Kutato Intezete Y kwi) Prelettani Osztalyanak (Igazgato: lbasznyak Istvan dr. Akademi structure-activity relationship, theories & study nathods Min)) LEMMR2, K. Uhemistry of glycocyamidines. P. 59 KOZLEMENYEI. xudapest, Hungary. Vol. 12, no. 1, 1959 Monthly list of East European Accessiona (EEAI). ZU. Vol. 9, no. 1, Jan., 196o. Uncl. IRUM, K. LEMPIW-SRETER, M.; --------------- On the dissociation of N-(B.B.B.~-trifluoretbyl)-ptosylamides and of N- (p-tosl) - phenacylamines from ammonia. A preliminary report. In German. ACTA CBIIIICA. (Magyar Tudpmanyos Akademia) Budapest, Hungary. Vol. 21, No. 1. 1959- Monthly List of East European Accessions (EEAI) LC vol. 9., No. 2., Feb.1960,, Uncl. 110 Distr: 4E3d 70eavage of N-(2,2 2-I.TifluoroethP)- and N-phenacyl-p- toluEnesulfonamide ~ in ammonia. M. Lempert--!7re-ter --and K. Lem Tiniv., Budapest). Ada' rmpT (L. F-6tvr* Hu-ng--71-,'8T-=950)(in German).- Chimt~r~ arried out (several hrs Cleavage of the title comptis. was c at 230-40*) in a sealed tube Nvith aq. NH~. In both cases: V12 p-toluenesulfonamide. rn. 135-6*, was obtained (in quant.~ yield from the first title compd. and in 57% yield from the wond). Thus, cleavage occurred at the C-N bond. Walter Dil~, T-V fPFdIT Karoly;_)PREUER, Judit; LEMPERTNE SRZTE-R, Magda; PATAKY, Istvan; FF~IMR, Klara Hydantoins, thiohydantoins, glycocyamidines. Pts. 1-2. Magy kem fcrlyoir 65 no.3:107-323 Mr 159. 1. Magyar Tudomanyoo Akademia Kiserleti Orvostudomanyi Kutato Intezete-Korelettani Osztalya., Budapest, Eotvos Lorand Tudo- manypgyetem Szerves-Kemiai Intezete, Budapest, Orvostudomanyi Egyetem Gyogyszertani Intezete, Budapest. H'jl-!CY% R-L" Ci ry, 3 t y 19-1 im. o 2 JOUR, R71 j --t K. L mp :in toins (1 ;,in 'Cloi I I Ile por T I., orj.."jtj_: t..!.(jn 'n tlia Pu F! FA c No abstr---ct. Ser:j LR-IIPERT, Karoly; BREUER, Judit ~ Hydantoins, Thiohydantoins, glycocyamidines. Pt. 4. Magy kem folyoir 65 no. 7: 263-264 JI '59. 1. l4agyar Tudomanyos Akademia Kiserleti Orvostudomanyi Inte- zete Korelattani Osztalya. IM4PERT, Karoly, a kemiai tudomanyok kandidatusa, Chemistry of 2-thiouracils, isocytosines and their condensed deriva- tives(auinazoline, thiazole-pyrimidine, and imidazole-pyrimidine analogs). Kem tud koz1 MTA 16 no.4:1,07-4U 161. 1. Magyar Tudomanyos Akademia Kiserleti Orvostudomanyi Kutato Intezete Koreletani Osztalya, Budapest. Cytosine) (Quinazoline) (P~rimidines) (Thiazole) kImidazole) LEMPERTHE, Sreter, Magda; KNAUSZ, Dezso; LEMPERT, Karoly -- -1 1 1---------- -- Alkvlation, dealkylation and alk7lation by ammonia and amines of the 5, 5-diethvlbarbituric acid 2-imides. YaU kem folyoir 67 no.3:115-119 Mr 161. 1. Eotvos Lorand Tudomanyegyetem Szerves Kemiai Intezete es Magyar Tudomanyos Akademia Kiserleti Orvostudomanyi Kutato Intezete, Korelettani Csztaly. LFMPERT, Karoly Chemistry of 2-thiouracils, isocytosines and their condensed derivatives analogons of quinazoline., thiazolopyrimidine, and imidazbpyrimidine (series). Pt. Ii. (to be contd) Kem tud kozl MTA 18 no. 1:37-11.2 162. i 1. A kemlai tudomanyok kandidatusa; Magyar Tudomanyos Akadaftia Orvostudo- manyi, Kul,-sto Intezete Korelettani Osztalya, Budapest. IMIMRT, Karoly., a kemiai tudomanyok kandidatusa Chemistry of 2-thiouracils, isocytosines and their condensed derivativesy analogons of quinazoline, thiazolopyrimidine, and imidazopyrimidine series). Pt.II.(To be contd.) Kem tud kczl VW-zLo.1:37-lU 162, 1. l4agyar Tudomanyos Akademia Orvostudomanyi Kutato Intezetet Korelettani Osztalya, Budapest. LEMPM,_ Karoly, a kemiai tudomanyok kandidatusa Chemistry of 2-thiouracyls, isocytosines and their condensed derivatives (Analogues of quinazoline, thiazolopyrimidine., and imidazopyrimidine-series, etc.).III. Kea tud kozl MTA 18 no.2t243-300 162. 1. Magyar Tudomanyos Akademia Kiserleti Orvostudomanyi Kutato Intezete Korelettani Oaztalya, Budapest. --. IMEERT, Karoly; BREUER, juijit A-U:Vlation, realkylation and dealkY3Ation of 2-amino-4- quinazoUnol by amines and amonia. Ma kem folyoir 68 no.lq: 452-454 0 162. %9y 1. Magyar Tudommiyos Akademia. Kisorleti Orvostudomanyi Into- zoto Korelettani Oaztalya. IM4KEMY K. (Budapest, XI., Gellert ter 4); IMPERT-SRETER, M. (Budapest, XI., Gellert ter 4); BREUPER, J. (Budapest., XI., Gellert ter 4) Hydantoin, thiohydantoin, glycocyamidine, Pt- 13. Periodica polytechn chem 7 bo.1;7-19 163. 1. lehratuhl fur Organische Chemie, Teehnische Universitat, Budapest (for K. Lempert). 2, Institut fur Organische Chemie der F-otvos-Lorand Universitat., Budapest (for Lempert-Sreter). 3. Institut fur Experimentelle Pledizinische Forschung der Ungarischen Akademie der Wissenschaften, Abteilung fur Pathophysiologie,, Budapest (for Breuer). LEMPERTA-K..(Budapest, XI., Gellert ter 4); BREUER, J. (Budapest, Viii., Koranyi Sandor u.2/a) Hydantoin, thiohydantoin, glycocyamidine. Pt. 15. Periodica polytechn chem 7 no.4:299-310 163. 1. Lehrstilll fur Organische Chemie, Technische Universitat, Budapest ifor Lempert). 2. Abteilung fur Pathophysiologie des Instituts fur Experimentelle Medizinische Forschung der Ungarischen Akademie der Wissenschaften, Budapest (for Breuer). FODOR) Gaborp akademikus; BEIM, Denesne; BITE, Pal, kandidatus; DOBO, Pal; FARKA5, Lorant, kandidatus; F. VARGA, Eva; IEKI'a-T' Karoly, lu3ndidatus; '0TV09-j-.I,aszlo, kandidatus; SZAflTAY, Csaba., Ta-iaiaatus; =11, Ferenc An account of the Prague Symposium on Natural Organic Compounds. Kem tud kozl 14TA 19 no.1:0,5-103 163. 1. Magyar Tudomanyos Akademia Sztereokemiai Kutato Csoportja, Budapest (for Fodor, Beke., Lempert, Otvos, Uresch). 2. MaErar Tudomanyos Akademia Kemiai Tudomanyok Osztalya (for Bite, Dobo, Farkas, F. Varga, Szantay). 3. "A Magyar Tudomanyos Akademia Kemiai Tudomanyok Osztalyanak Kozlemenyei" szerkeszto bizottsagi tagja (for Fodor). IZZIPERT, Karoly, kandidatus Repott on the discussion of the disaertation prepared by Elmer Vinkler for obtaining the title of doctor of chemical sciences. Kom tud kozl WA 20 no.4-474-477 163. IEMPERTj,"c ; I.EMPERTNE SRE7ER, Magda; BREUER, Judit; PATAKI, lotvwl; -rywlFzn, A.Kiara, -'Hydantoins, thiobydantoins, glycocyamidines. Pt.11. Magy kem folyoir 69 no.4tl43-149 Ap 163. 1. Magyar Tudoma.Wos Akademia Kiserleti Orvostudomanvi Kutato Intezete Koreilettani Osatalva, Budapest; Hotvos Lorand Tudomanyegyatem Szerves- Kemiai Tanozeke es Budapeati Orvostudomanyi Egyetem Gyogyszertani Intesete. Karoly: bi-~LUER, Judit Hydantohiu, thiobydantoino, glycocyamidines.Ft.15. Magy kem fol:7oir 69 no.7:3"-1)-)28 Jl 163. 1. 13ud!.r,,ijti Diuozaki Egyetom Szerves-Kemiai Tanszeke as a Iflagyar Tudo- manyos ilkadoidu Kiserlotui Orvostudomanyi Intozete Korelettani Osztalya. ILZIPERT . Karoly; LCILL-CRI.LL, Gabor Imidazoquinezolinediones. ?t.2. Magy kem folyoir 69 no.9: 387-390 S 163. 1. Budapest-A flusza-ki ECyet----r,-L ~..zerves-Kemiai Tanszeke. LEMPERT K 'I dr. (Budapcs~,, XI., Gollort ter Ij-); ZAIJER, Karaly (Budapest, Judith (Budapest, Vill., Koranyi Sandor Tert ter 4); BREUERY u.; /,a) ' ' Hydantoins, thiohydantoins, g1jeocyanidines. Pt. 17. Periodica polytechn chem 8 no.1:21-28 164. 1. Department of Organic Chemistry, Folytechnical University, Budapest (for Lemport and Zauer). 2. Department of Pathophysiology, Institute of Experimental Medical Rpsearch of the Hungarian Academy of Sciences, Budapest (for Breuer). DOLESCHALL, Gabor., dr. (Budapest,XI.pGellert ter 4); LEMPERT, Karoly, dr. (Budapeat,XI., Gellert ter 4) 3.1,4H-benz6c,azin-4-ones. Pt. 4. Acta chimica Hung 40 no. 2: 235-243 164. 1. Department of Organic Cheuistry, Budapest Technical University. AU7,70": L --Doloshall, G. (Doctor) __Ir-,r,,3rt K~aro (Doctor) 0`13: bo-i3al-t-r-nt of Organic Chomstry, Technical University F~)Hapost III. fl-alkyl derivatives and sow related compounds SOURC.": Acadr-mia scientiarum hungaricae, Acta chimicax v. 45, no. 4, 1965, 357-368 TOFIC TAGS: organic azo, compound, organic synthetic compound, ester, organic amide, amino ABSTRACT: Starting from the ester or amide of (2-mothylthio-),Li-dihydro-4-oxo-3-quinazolinyl)-acetic acid, various 2,5 (111, 30-imidazo [2,1-b] quinazolinedionesL'gpbstituted in the 1 position have boon prepared by ring closure effected by primary amines. Analogously, starting from the corresponding (I-quinazolinyl)- acetamide, 2,5 ('LH, 3H)-imidazo [1,2-a] quinazolinediones substituted in position 3 have been synthesized. l-Alkyl-2-alkylmercapto-1f(lH)- quinazolinono6, intermediate products used in these synth '06eS, showed a risingly high reactivity with nucleophilic reagents. The authors thank Dr.-p. .Loffhsfor the IR and Dr. L. Lany: for the UV sPectra, Mrs.' I. Balogh-Batta and staff for the microanalysos, and Dr. If. E- DUOU (Smitli Kline and French Laboratories, Philadelphia) for the chemotherapeutic tests. fOrig. art. in En&--7 5PRS: 33,�0-67 SUB CODE: 07 SUB14 DATE: 19Nov64 / ORIG REF: 002 Co / OTH REF: 006