An efficient, diversity-oriented approach to novel steroid analogues possessing a C-5β configuration begins with the Stille cross-coupling of enantiomerically pure cycloalkenylstannane trans-2 and enol triflate 3. The resulting diene trans-4 engages in
A new class of sugar-oxasteroid-quinone hybrid molecules has been designed and synthesized involving...
Herein is reported the synthesis of molecular probes for action of neuroactive steroids in vitro and...
Although the Diels-Alder (DA) reaction of 2-cyclohexenones and 1,3-dienes is in principle an elegant...
Various steroid analogues were synthesized by Stille coupling of bicyclo[4.3.0]nonenylstannanes cis-...
The Diels-Alder reaction is widely acknowledged to be one of the most synthetically useful reactions...
Unprecedented cholestane analogs have been synthesized by Diels-Alder reactions between a diene gene...
This review explores the myriad ways in which the Diels-Alder reaction has been employed in the cons...
A sequential enyne-metathesis/Diels-Alder strategy is reported for the synthesis of a new class of s...
The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a lin...
The bromobenzene-derived and enantiopure cis-1,2-dihydrocatechol 2 can be elaborated, via Diels-Alde...
Bunte JO, Rinne S, Mattay J. Synthesis of novel steroid backbones via photoinduced electron transfer...
International audienceA diversity-oriented synthesis (DOS) approach has been used to functionalize 1...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
In this paper the applicability of the Stille-coupling reaction for the synthesis of a variety of ol...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
A new class of sugar-oxasteroid-quinone hybrid molecules has been designed and synthesized involving...
Herein is reported the synthesis of molecular probes for action of neuroactive steroids in vitro and...
Although the Diels-Alder (DA) reaction of 2-cyclohexenones and 1,3-dienes is in principle an elegant...
Various steroid analogues were synthesized by Stille coupling of bicyclo[4.3.0]nonenylstannanes cis-...
The Diels-Alder reaction is widely acknowledged to be one of the most synthetically useful reactions...
Unprecedented cholestane analogs have been synthesized by Diels-Alder reactions between a diene gene...
This review explores the myriad ways in which the Diels-Alder reaction has been employed in the cons...
A sequential enyne-metathesis/Diels-Alder strategy is reported for the synthesis of a new class of s...
The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a lin...
The bromobenzene-derived and enantiopure cis-1,2-dihydrocatechol 2 can be elaborated, via Diels-Alde...
Bunte JO, Rinne S, Mattay J. Synthesis of novel steroid backbones via photoinduced electron transfer...
International audienceA diversity-oriented synthesis (DOS) approach has been used to functionalize 1...
Stille reaction is one of the most common, efficient and selective Pd-catalyzed cross-coupling react...
In this paper the applicability of the Stille-coupling reaction for the synthesis of a variety of ol...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
A new class of sugar-oxasteroid-quinone hybrid molecules has been designed and synthesized involving...
Herein is reported the synthesis of molecular probes for action of neuroactive steroids in vitro and...
Although the Diels-Alder (DA) reaction of 2-cyclohexenones and 1,3-dienes is in principle an elegant...