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

Academic Article
Publication Date:
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.
Iris type:
01.01 Articolo in rivista
Keywords:
PENICILLIUM SP; 1ST SYNTHESIS; ACID; LACTONE; METHYLENOLACTOCIN; STEREOCHEMISTRY; ADDITIONS; CHEMISTRY; ESTERS
List of contributors:
Handle:
https://iris.cnr.it/handle/20.500.14243/268618
Published in:
CHEMICAL COMMUNICATIONS (LOND., 1996, PRINT)
Journal