Zobrazeno 1 - 6
of 6
pro vyhledávání: '"György Jeges"'
Publikováno v:
Journal of Molecular Catalysis A: Chemical. 165:89-96
Homogeneous catalytic hydrosilylation of pregn-16-en-20-yne (produced from 17-iodo-5α-androst-16-ene by Stille-coupling) with triethylsilane is investigated in the presence of various Pt, Pd and Rh complexes. The stereoselective Diels–Alder reacti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9c3f65f2a1c1f5bad5d9ee462fd6df84
https://doi.org/10.1016/s1381-1169(00)00439-8
https://doi.org/10.1016/s1381-1169(00)00439-8
Autor:
Kurt Mereiter, Walter Weissensteiner, László Kollár, György Petőlz, Tamás Kégl, György Jeges, Thomas Sturm
Publikováno v:
Journal of Organometallic Chemistry. 595:93-101
Platinum complexes PtCl2(L) and PtCl(SnCl3)(L) of the ferrocenyl diphosphine ligands (L) (R,R)-1-diphenylphosphino-2,1′-[(1-diphenylphosphino)-1,3-propanediyl]-ferrocene (1), (R,R)-1-diphenylphosphino-2,1′-[(1-dicyclohexylphosphino)-1,3-propanedi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c1a081415fd8a555e2dfbddecefafb2
https://doi.org/10.1016/s0022-328x(99)00584-7
https://doi.org/10.1016/s0022-328x(99)00584-7
Publikováno v:
Tetrahedron. 54:6767-6780
Steroidal alkenyl iodides (17-iodo-androsta-16-ene and 17-iodo-4-methyl-4-aza-androsta-16-ene-3-one) were reacted with conjugated unsaturated esters (ethyl acrylate, diethyl fumarate, diethyl maleate, diethyl acetylene dicarboxylate) in Heck-reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75e0c15ad83c0b3938b920442e7b3f77
https://doi.org/10.1016/s0040-4020(98)00361-5
https://doi.org/10.1016/s0040-4020(98)00361-5
Publikováno v:
The Journal of Organic Chemistry. 62:1326-1332
Tandem Stille coupling and Diels−Alder reaction of steroidal iodoalkenyl substrates [17-iodoandrosta-16-ene (2), 17-iodo-3-keto-4-methyl-4-azaandrosta-16-ene (10), and 17-iodo-3-keto-4-azaandrosta-16-ene (11)] were examined in the presence of vinyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::397f76da0a5375ee8dcc06ff19ce5473
https://doi.org/10.1021/jo9615256
https://doi.org/10.1021/jo9615256
Publikováno v:
Tetrahedron Letters. 37:2085-2088
Novel androstane-based skeletons were synthesized in a facile one-pot reaction of 17-iodo-androsta-16-ene, vinyltributylstannane and functionalised olefins. The palladium-catalysed coupling reaction was followed by Diels-Alder reaction resulting in t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fffb47a7395ae1d703f0da8321a631d
https://doi.org/10.1016/0040-4039(96)00199-2
https://doi.org/10.1016/0040-4039(96)00199-2
Publikováno v:
ChemInform. 29
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69c008a8539ff77da47b306e18f0c127
https://doi.org/10.1002/chin.199841191
https://doi.org/10.1002/chin.199841191