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.

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

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.
1998
PENICILLIUM SP; 1ST SYNTHESIS; ACID; LACTONE; METHYLENOLACTOCIN; STEREOCHEMISTRY; ADDITIONS; CHEMISTRY; ESTERS
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/268618
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