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Issue 63, 2015
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Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: synthesis of trans-2,3-disubstitued indolines

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Abstract

Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates has been achieved, giving trans-2,3-disubstitued indolines as major diastereoisomers in moderate to good yields.

Graphical abstract: Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: synthesis of trans-2,3-disubstitued indolines

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Article information


Submitted
25 May 2015
Accepted
02 Jul 2015
First published
06 Jul 2015

Chem. Commun., 2015,51, 12653-12656
Article type
Communication

Phosphine-catalyzed [4+1] annulation of 2-tosylaminochalcones with allenoates: synthesis of trans-2,3-disubstitued indolines

Z. Gao, C. Wang, C. Yuan, L. Zhou, Y. Xiao and H. Guo, Chem. Commun., 2015, 51, 12653
DOI: 10.1039/C5CC04279H

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