Cycloaddition chemistry of carbonyl ylides for alkaloid synthesis


如何引用文章

全文:

开放存取 开放存取
受限制的访问 ##reader.subscriptionAccessGranted##
受限制的访问 订阅存取

详细

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.

作者简介

A. Padwa

Department of Chemistry, Emory University

编辑信件的主要联系方式.
Email: chemap@emory.edu
美国, Atlanta, GA

补充文件

附件文件
动作
1. JATS XML

版权所有 © Springer Science+Business Media New York, 2016