Direct amino-phenylselenylation of enoates: an easy route to alpha-phenylseleno-beta-amino esters and beta-lactams.
Academic Article
Publication Date:
1998
abstract:
A "one-pot" procedure to obtain alpha-phenylseleno-beta-amino esters from the corresponding enoates is described. The target compounds are useful synthetic tools and direct precursors of new alpha-phenylseleno-beta-lactams, which can be easily transformed into their alpha-alkylidene analogues. (C) 1998 Elsevier Science Ltd. All rights reserved.
Iris type:
01.01 Articolo in rivista
Keywords:
selenium and compounds; amino acids and derivatives; azetidinones; Michael reactions; cyclisation
List of contributors:
D'Onofrio, Franco
Published in: