Title of article
Enantioselective synthesis of a trans-ethenyl-hydrindene, a useful steroid CD-ring diene precursor
Author/Authors
Di Filippo، نويسنده , , Marcello and Izzo، نويسنده , , Irene and Vece، نويسنده , , Alessandro and De Riccardis، نويسنده , , Francesco and Sodano، نويسنده , , Guido، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
3
From page
1155
To page
1157
Abstract
A highly efficient enantioselective synthesis of protected trans-hydrindenol diene 1 is described starting from the readily available Hajos–Parrish ketone. The reported methodology represents the most convenient route (10 steps, 31% overall yield) to both enantiomeric forms of a steroid (estrogenic) CD-ring diene precursor.
Keywords
asymmetric synthesis , Dienes , Stille reaction , Steroids
Journal title
Tetrahedron Letters
Serial Year
2001
Journal title
Tetrahedron Letters
Record number
1641822
Link To Document