The use of N-sulfenylimines in the β-lactam synthon method: Staudinger reaction, oxidation of the cycloadducts and ring opening of β-lactams-Reference-Cited by-同舟云学术

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The use of N-sulfenylimines in the β-lactam synthon method: Staudinger reaction, oxidation of the cycloadducts and ring opening of β-lactams

Published:2007-04 Issue:15 Volume:63 Page:3205-3216
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Coantic Stéphanie,Mouysset Dominique,Mignani Serge,Tabart Michel,Stella Lucien

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference51 articles.

1. Antibiotics Containing the β-Lactam Structure, Parts 1&2,1983

2. Recent Advances in the Chemistry of Anti-Infective Agents,1993

3. Quinolone, Everninomycin, Glycylcycline, Carbapenem, Lipopeptide and Cephem Antibacterials in Clinical Development

4. The Chemistry of β-Lactams,1992

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