Issue 2, 1998

Tandem Michael-aldol induced ring closure of dimethyl 2-phenylselenofumarate: a diastereoselective entry to novel 4-phenylseleno butano-4-lactone derivatives, versatile precursors of naturally occurring compounds

Abstract

Tandem Michael-aldol induced ring closure of dimethyl 2-phenylsenofumarate gives, with good yields and diastereoselectivities, highly substituted 4-phenylselenobutano-4-lactones, which can be further transformed into naturally occurring substances.

Article information

Article type
Paper

Chem. Commun., 1998, 185-186

Tandem Michael-aldol induced ring closure of dimethyl 2-phenylselenofumarate: a diastereoselective entry to novel 4-phenylseleno butano-4-lactone derivatives, versatile precursors of naturally occurring compounds

R. Margarita, L. Parlanti, G. Piancatelli and M. Sbraga, Chem. Commun., 1998, 185 DOI: 10.1039/A707148E

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