Title of article :
Divergent synthesis of pseudoenantiomers for ABC-ring moiety of steroids
Author/Authors :
Furuta، نويسنده , , Miyu and Hanaya، نويسنده , , Kengo and Sugai، نويسنده , , Takeshi and Shoji، نويسنده , , Mitsuru، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2014
Pages :
3
From page :
3189
To page :
3191
Abstract :
Steroid family has various bioactivities and characteristic polycyclic structure. Although several synthetic methods have been reported, more efficient way is desired for medicinal chemistry. In this Letter, we synthesized pseudoenantiomers of tricyclic enones toward both enantiomers for ABC-ring moiety of steroids utilizing d-mannitol as a chiral source. The key steps are radical domino cyclization of polyalkenyl-β-keto ester into tricyclic keto ester and subsequent dealkoxycarbonylation.
Keywords :
Steroid , radical cyclization , Domino reaction , Dealkoxycarbonylation , ?-keto ester
Journal title :
Tetrahedron Letters
Serial Year :
2014
Journal title :
Tetrahedron Letters
Record number :
1889561
Link To Document :
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