Molecular iodine induced/1,3-dipolar cycloaddition/oxidative aromatization sequence: an efficient strategy to construct 2-substituted benzo[f]isoindole-1,3-dicarboxylates-Reference-Cited by-同舟云学术

Molecular iodine induced/1,3-dipolar cycloaddition/oxidative aromatization sequence: an efficient strategy to construct 2-substituted benzo[f]isoindole-1,3-dicarboxylates

Published:2014 Issue:30 Volume:4 Page:15526-15533
ISSN:2046-2069
Container-title:RSC Adv.
language:en
Short-container-title:RSC Adv.

Author:

Huang Huan-Ming¹²³,Gao Jian-Rong¹²³,Ye Qing¹²³,Yu Wu-Bin¹²³,Sheng Wei-Jian¹²³,Li Yu-Jin¹²³

Affiliation:

1. Key Laboratory Breeding Base of Green Chemistry-Synthesis Technology

2. Zhejiang University of Technology

3. Hangzhou, P. R. China

Abstract

A useful method for a molecular iodine induced 1,3-dipolar cycloaddition/oxidative aromatization sequence to construct 2-substituted-benzo[f]isoindole-1,3-dicarboxylates is reported.

Publisher

Royal Society of Chemistry (RSC)

Subject

General Chemical Engineering,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2014/RA/C4RA01593B

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