Zobrazeno 1 - 10
of 64
pro vyhledávání: '"Mihailo Lj. Mihailović"'
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 97:1095-1100
The lead tetraacetate oxidation of (Z)-5, 10-secocholest-1(10)-ene-3β,5α−diol 3-acetate (1) gave products arising from: (i) conversion of the 5α−hydroxy group to the ketone function (2), (ii) intramolecular cyclization (to the 2α,5α−tetrah
Autor:
Aleksandar V. Teodorovic, Biljana M. Mojsilovic, Mihailo Lj. Mihailović, Milan D. Joksović, S. Konstantinovic
Publikováno v:
Monatshefte fuer Chemie/Chemical Monthly. 131:0091-0095
Acetophenone, 2,2-dimethylcyclopentanone, 3,3-dimethyl-2-butanone, 3-methyl-2-butanone, and 2-pentanone were reduced with borane mediated by (S)-alanine, (S)-methionine, (S)-leucine, (S)-valine, and (S)-isoleucine in very good yields giving predomina
Autor:
Rastko D. Vukićević, Stanimir Konstantinovic, Zoran Marković, Mihailo Lj. Mihailović, Ljubinka Joksović
Publikováno v:
Scopus-Elsevier
The acylation of some alicyclic and aliphatic alkenes by the electrochemical generation of a catalyst using a sacrificial aluminum anode was investigated. Substrates were electrolyzed in a dichloromethane solution of an appropriate electrolyte (tetra
Autor:
Mihailo Lj. Mihailović, Aleksandar Z̆. Milovanović, Bernard Tinant, Jean-Paul Declercq, Lj. Lorenc, Vladimir D. Pavlović, M. Rajkovic
Publikováno v:
Tetrahedron. 52:11995-12008
The (Z)-19-nor-5,10-secosteroidal ketone 11 reacts with hydroxylamine hydrochloride to give the (E)- and (Z)-oximes 12 and 13, while with N-methylhydroxylamine hydrochloride it undergoes transannular nitrone 1,3-dipolar cycloaddition to give isoxazol
Autor:
Hermann Fuhrer, L. Lorenc, Mihailo Lj. Mihailović, Roland Heckendorn, Jaroslav Kalvoda, Vladimir D. Pavlović
Publikováno v:
Helvetica Chimica Acta. 78:1291-1297
The structures 9 and 8 are proposed for the single isolated irradiation product of 5-oxo-5,10-secocholest-1(10)-en-3α-yl acetate (6) [2] and for the minor product of irradiation of 5-oxo-5,10-secocholest-1(10)-en-3β-yl acetate (1) [3], respectively
Publikováno v:
Helvetica Chimica Acta. 76:2254-2262
UV Irradiation of (Z)- and (E)-1(10)-unsaturated 5,10-secosteroids 1–4 in acetone solution effected, besides (Z/E)-isomerization, (i) a stereospecific epoxidation (only in the presence of O2), which, depending on the configuration ((Z) or (E)) in t
Autor:
Lj. Lorenc, Bernard Tinant, Aleksandar Z̆. Milovanović, Mihailo Lj. Mihailović, M. Rajkovic, Jean-Paul Declercq
Publikováno v:
ChemInform. 24
Autor:
Hermann Fuhrer, L. Lorenc, Vladimir D. Pavlović, Jaroslav Kalvoda, Mihailo Lj. Mihailović, Roland Heckendorn
Publikováno v:
ChemInform. 26
The structures 9 and 8 are proposed for the single isolated irradiation product of 5-oxo-5,10-secocholest-1(10)-en-3α-yl acetate (6) [2] and for the minor product of irradiation of 5-oxo-5,10-secocholest-1(10)-en-3β-yl acetate (1) [3], respectively
Publikováno v:
ChemInform. 26
Autor:
Jean-Paul Declercq, Lj. Lorenc, Mihailo Lj. Mihailović, Bernard Tinant, Vladimir D. Pavlović, Aleksandar Z̆. Milovanović, M. Rajkovic
Publikováno v:
ChemInform. 28
The (Z)-19-nor-5,10-secosteroidal ketone 11 reacts with hydroxylamine hydrochloride to give the (E)- and (Z)-oximes 12 and 13, while with N-methylhydroxylamine hydrochloride it undergoes transannular nitrone 1,3-dipolar cycloaddition to give isoxazol