A flexible route to 4-substituted β-lactams

Béatrice Quiclet-Sire; Samir Z. Zard

doi:10.3987/COM-10-S(E)39

A flexible route to 4-substituted β-lactams

Béatrice Quiclet-Sire
, Samir Z. Zard

Laboratoire de Synthèse Organique

Résultats de recherche: Contribution à un journal › Article › Revue par des pairs

Résumé

A variety of 4-substituted β-lactams can be readily prepared by the radical addition-transfer of 4-S-xanthyl-azetidinones to unactivated olefins. For this radical chain process to operate efficiently it is necessary to place an acyl group on the nitrogen of the azetidinone ring.

langue originale	Anglais
Pages (de - à)	263-271
Nombre de pages	9
journal	Heterocycles
Volume	82
Numéro de publication	1
Les DOIs	https://doi.org/10.3987/COM-10-S(E)39
état	Publié - 1 déc. 2010
Modification externe	Oui

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10.3987/COM-10-S(E)39

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abstract = "A variety of 4-substituted β-lactams can be readily prepared by the radical addition-transfer of 4-S-xanthyl-azetidinones to unactivated olefins. For this radical chain process to operate efficiently it is necessary to place an acyl group on the nitrogen of the azetidinone ring.",

author = "B{\'e}atrice Quiclet-Sire and Zard, \{Samir Z.\}",

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AB - A variety of 4-substituted β-lactams can be readily prepared by the radical addition-transfer of 4-S-xanthyl-azetidinones to unactivated olefins. For this radical chain process to operate efficiently it is necessary to place an acyl group on the nitrogen of the azetidinone ring.

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DO - 10.3987/COM-10-S(E)39

M3 - Article

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VL - 82

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JF - Heterocycles

IS - 1

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A flexible route to 4-substituted β-lactams

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