Issue 23, 2015

Mild arylboronic acid catalyzed selective [4 + 3] cycloadditions: access to cyclohepta[b]benzofurans and cyclohepta[b]indoles

Abstract

The first example of arylboronic acid catalyzed [4 + 3] cycloaddition reaction is reported. 3,5-Bis-(trifluoromethyl) phenylboronic acid is shown to be the best catalyst in this reaction. The method has also enabled the preparation of cyclohepta[b]benzofurans and cyclohepta[b]indoles in excellent yields.

Graphical abstract: Mild arylboronic acid catalyzed selective [4 + 3] cycloadditions: access to cyclohepta[b]benzofurans and cyclohepta[b]indoles

Supplementary files

Article information

Article type
Communication
Submitted
02 Apr 2015
Accepted
05 May 2015
First published
05 May 2015

Org. Biomol. Chem., 2015,13, 6449-6452

Mild arylboronic acid catalyzed selective [4 + 3] cycloadditions: access to cyclohepta[b]benzofurans and cyclohepta[b]indoles

K. Cao, H. Bian and W. Zheng, Org. Biomol. Chem., 2015, 13, 6449 DOI: 10.1039/C5OB00653H

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