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
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