Title of article :
Aziridination of 11-pregnene-3,20-dione using PhIN-Ses
Author/Authors :
Di Chenna، نويسنده , , Pablo H and Dauban، نويسنده , , Philippe and Ghini، نويسنده , , Alberto and Burton، نويسنده , , Gerardo and Dodd، نويسنده , , Robert H، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2000
Pages :
5
From page :
7041
To page :
7045
Abstract :
The copper-catalyzed reaction of [N-(Ses)imino]phenyliodinane with 11-pregnene-3,20-dione gave the corresponding aziridine in 53% yield. The Ses protecting group could be conveniently removed using the TASF reagent. Furthermore, nucleophilic ring opening of the protected N-Ses-aziridine with thiophenol in the presence of a Lewis acid led to introduction of the thiophenol group at the α-12 position but, unexpectedly, concomitant loss of the Ses group to provide compound 10.
Journal title :
Tetrahedron Letters
Serial Year :
2000
Journal title :
Tetrahedron Letters
Record number :
1642429
Link To Document :
بازگشت