Cycloaddition chemistry of carbonyl ylides for alkaloid synthesis


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Resumo

As highlighted in this mini-review, a growing area of interest in organic synthesis involves the use of substituted carbonyl ylides as 1,3-dipoles for the preparation of alkaloidal natural products. Cascade reactions proceeding by an intramolecular 1,3-dipolar cycloaddition of carbonyl ylides are of particular interest to the synthetic organic community because of the increase in molecular complexity involved and the high isolated yields.

Sobre autores

A. Padwa

Department of Chemistry, Emory University

Autor responsável pela correspondência
Email: chemap@emory.edu
Estados Unidos da América, Atlanta, GA

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