2,5-Disubstituted pyrrolidines: synthesis by enamine reduction and subsequent regioselective and diastereoselective alkylations.

Methodology for the diastereoselective synthesis of 2,5-disubstituted pyrrolidines by reduction of enamines derived from pyroglutamic acid is reported; the nature of nitrogen protection was found to be critical for the stereochemical control of the reaction outcome. Regioselective manipulation of th...

وصف كامل

التفاصيل البيبلوغرافية
المؤلفون الرئيسيون: Hussaini, SR, Moloney, M
التنسيق: Journal article
اللغة:English
منشور في: 2006