Spiro[pyrrolidine-2,3′-oxindole] derivatives synthesized by novel regionselective 1,3-dipolar cycloadditions

被引：0
作者：
Gang Chen
Jing Yang
Suo Gao
Hongping He
Shunlin Li
Yingtong Di
Ying Chang
Yang Lu
Xiaojiang Hao
机构：
[1] Kunming Institute of Botany,State Key Laboratory of Phytochemistry and Plant Resources in West China
[2] Chinese Academy of Sciences,School of Chemistry and Chemical Engineering
[3] Shanghai Jiaotong University,Institute of Materia Medica
[4] Chinese Academy of Medical Sciences,College of Chemistry and Chemical Engineering
[5] Xi’an Shiyou University,undefined
来源：
Molecular Diversity | 2012年 / 16卷
关键词：
1,3-dipolar cycloaddition; Huisgen reaction; Regioisomers; Spiro compounds; Nitro group;
D O I：
暂无
中图分类号：
学科分类号：
摘要：
A series of spiro-oxindole derivatives was synthesized by novel regioselective 1,3-dipolar cycloadditions of isatin, α-amino acids, and (E)-β-aryl-nitro-olefins. Regioisomers were produced in each reaction and the major products showed different regioselectivity compared to previously reported spiro-oxindole derivatives.
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页码：151 / 156
页数：5
相关论文
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