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

Jixuan Liang; Jingbo Chen; Jianping Liu; Liang Li; Hongbin Zhang

doi:10.1039/c001465f

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

Chem Commun (Camb). 2010 Jun 7;46(21):3666-8. doi: 10.1039/c001465f. Epub 2010 Apr 16.

Authors

Jixuan Liang¹, Jingbo Chen, Jianping Liu, Liang Li, Hongbin Zhang

Affiliation

¹ Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming, Yunnan 650091, PR China.

PMID: 20396830
DOI: 10.1039/c001465f

Abstract

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

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Alkaloids / chemical synthesis*
Alkaloids / chemistry
Erythrina / chemistry*
Indoles / chemical synthesis*
Indoles / chemistry
Oxidation-Reduction
Oxindoles

Substances

Alkaloids
Indoles
Oxindoles
2-oxindole