Unprecedented cholestane analogs have been synthesized by Diels-Alder reactions between a diene generated in high yields from vitamin D3 and appropriate dienophiles. This strategy is useful for the scarcely utilized A+CD → ABCD approach to the tetracyclic steroid nucleus
The recent development of a hydroxy-directed Diels-Alder reaction, which enables control of both reg...
An efficient, diversity-oriented approach to novel steroid analogues possessing a C-5β configuration...
Cholesta-5,8-dien-3\u3b2-ol was synthesized in two steps by starting from 3\u3b2-acetoxycholesta-5,7...
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...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
The Diels-Alder reaction is widely acknowledged to be one of the most synthetically useful reactions...
The enantiospecific synthesis of the vitamin D-3 CD ring fragment 3 is reported. Key steps are the d...
Various steroid analogues were synthesized by Stille coupling of bicyclo[4.3.0]nonenylstannanes cis-...
The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a lin...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
International audienceLithium-mediated reductive dimerization of buta-1,3-diene in the presence of c...
The Diels-Alder reaction has become a prominent synthetic tool due to the effectiveness for which it...
A new approach for the construction of the C ring of an aromatic steroid, utilising the Diels-Alder ...
This thesis is divided into two parts. The first part describes the development ofmethodology for th...
The recent development of a hydroxy-directed Diels-Alder reaction, which enables control of both reg...
An efficient, diversity-oriented approach to novel steroid analogues possessing a C-5β configuration...
Cholesta-5,8-dien-3\u3b2-ol was synthesized in two steps by starting from 3\u3b2-acetoxycholesta-5,7...
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...
We report the combination of an intramolecular Diels-Alder (IMDA) reaction and a desymmetrisation pr...
The Diels-Alder reaction is widely acknowledged to be one of the most synthetically useful reactions...
The enantiospecific synthesis of the vitamin D-3 CD ring fragment 3 is reported. Key steps are the d...
Various steroid analogues were synthesized by Stille coupling of bicyclo[4.3.0]nonenylstannanes cis-...
The tetracarbocyclic framework of the nicandrenone natural products is formed in one step from a lin...
Diels-Alder (D-A) reaction is undoubtedly the most powerful [4 + 2] cycloaddition reaction in organi...
International audienceLithium-mediated reductive dimerization of buta-1,3-diene in the presence of c...
The Diels-Alder reaction has become a prominent synthetic tool due to the effectiveness for which it...
A new approach for the construction of the C ring of an aromatic steroid, utilising the Diels-Alder ...
This thesis is divided into two parts. The first part describes the development ofmethodology for th...
The recent development of a hydroxy-directed Diels-Alder reaction, which enables control of both reg...
An efficient, diversity-oriented approach to novel steroid analogues possessing a C-5β configuration...
Cholesta-5,8-dien-3\u3b2-ol was synthesized in two steps by starting from 3\u3b2-acetoxycholesta-5,7...
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