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.

Direct amino-phenylselenylation of enoates: an easy route to alpha-phenylseleno-beta-amino esters and beta-lactams.

D'Onofrio F;
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.
1998
selenium and compounds
amino acids and derivatives
azetidinones
Michael reactions
cyclisation
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/268611
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