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Stereoselective amination of chiral enolates: Synthesis of chiral key intermediates for β-lactam antibiotics

✍ Scribed by Carlos Cativiela; María D. Díaz-de-Villegas; José A. Galvéz

Book ID
108036221
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
276 KB
Volume
5
Category
Article
ISSN
0957-4166

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## Abstract The importance of the β‐lactam substructure is exemplified by the several classes of β‐lactam antibiotics. Among the synthetic routes available to obtain this interesting scaffold, the Kinugasa reaction is a convergent strategy. In this article, the synthesis of a variety of chiral β‐la