Issue 21, 2010
From the journal:

Chemical Communications

Oxidative dearomatization in the synthesis of erythrina, oxindole and hexahydropyrrolo[2,3-b]indole skeletons†

Jixuan Liang,a   Jingbo Chen,a   Jianping Liu,a   Liang Lia  and  Hongbin Zhang*a  

* Corresponding authors

a Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, PR China
E-mail: zhanghb@ynu.edu.cn, zhang_hongbin@hotmail.com

Abstract

New synthetic strategies leading to highly functional erythrina, oxindole and pyrrolidinoindoline skeletons have been developed and an efficient formal syntheses of (±)-demethoxyerythratidinone reported.

Graphical abstract: Oxidative dearomatization in the synthesis of erythrina, oxindole and hexahydropyrrolo[2,3-b]indole skeletons

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Article information

DOI
https://doi.org/10.1039/C001465F
Article type
Communication
Submitted
21 Jan 2010
Accepted
23 Mar 2010
First published
16 Apr 2010

Chem. Commun., 2010,46, 3666-3668

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Oxidative dearomatization in the synthesis of erythrina, oxindole and hexahydropyrrolo[2,3-b]indole skeletons

J. Liang, J. Chen, J. Liu, L. Li and H. Zhang, Chem. Commun., 2010, 46, 3666 DOI: 10.1039/C001465F

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