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
Articolo
Data di Pubblicazione:
1998
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.
Tipologia CRIS:
01.01 Articolo in rivista
Keywords:
PENICILLIUM SP; 1ST SYNTHESIS; ACID; LACTONE; METHYLENOLACTOCIN; STEREOCHEMISTRY; ADDITIONS; CHEMISTRY; ESTERS
Elenco autori:
D'Onofrio, Franco
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