A versatile method for the synthesis of 3-alkoxycarbonyl β-lactam derivatives

Journal of Organic Chemistry

Volumn 71, Issue 2, 2006, Pages 815-818

  Jiao, Lei ^a   Zhang, Qianfeng ^a   Liang, Yong ^a   Zhang, Shiwei ^a   Xu, Jiaxi ^a  

^a Peking University   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; CATALYST SELECTIVITY; REACTION KINETICS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

CYCLOADDITION REACTIONS; DIASTEREOSELECTIVITIES; LACTAM DERIVATIVES;

DERIVATIVES;

BETA LACTAM DERIVATIVE; CARBONYL DERIVATIVE; IMINE; KETENE DERIVATIVE;

ARTICLE; CYCLOADDITION; DESULFURIZATION; DIASTEREOISOMER; QUANTUM YIELD; REACTION ANALYSIS; STAUDINGER REACTION; STEREOCHEMISTRY; SYNTHESIS;

ALKYLATION; BETA-LACTAMS; ETHYLENES; INDICATORS AND REAGENTS; KETONES; MODELS, MOLECULAR; MOLECULAR CONFORMATION;

EID: 30844447687     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo052135z     Document Type: Article

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48. See Supporting Information for the additional discussion and experiments of trans selectivity in the desulfurization reactions.