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Volumn 66, Issue 5, 2001, Pages 1612-1620

Straightforward asymmetric entry to highly functionalized medium-sized rings fused to β-lactams via chemo- and stereocontrolled divergent radical cyclization of Baylis-Hillman adducts derived from 4-oxoazetidine-2-carbaldehydes

(3) Alcaide, B a Almendros, P a Aragoncillo, C a

a UNIVERSIDAD COMPLUTENSE DE MADRID (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

AZETIDINONE DERIVATIVE; BETA LACTAM ANTIBIOTIC; BICYCLO COMPOUND;

ARTICLE; CHEMICAL REACTION; CHEMICAL STRUCTURE; CHIRALITY; CYCLIZATION; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; STEREOCHEMISTRY; SYNTHESIS;

EID: 0035831074 PISSN: 00223263 EISSN: None Source Type: Journal
DOI: 10.1021/jo005715z Document Type: Article

Times cited : (83)

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