Issue 51, 2014

An efficient synthesis of highly substituted indanones and chalcones promoted by superacid

Abstract

A superacid promoted one-pot process for the efficient synthesis of indanones is presented. This process enabled the formation of a dual C–C bond between aryl isopropyl ketones and benzaldehydes. Interestingly, when the reaction was performed between acetophenones and benzaldehydes, it was impeded just after the aldol condensation and resulted in the corresponding chalcones.

Graphical abstract: An efficient synthesis of highly substituted indanones and chalcones promoted by superacid

Supplementary files

Article information

Article type
Communication
Submitted
01 Apr 2014
Accepted
06 Jun 2014
First published
09 Jun 2014
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2014,4, 26662-26666

Author version available

An efficient synthesis of highly substituted indanones and chalcones promoted by superacid

A. Das, A. G. Krishna Reddy, J. Krishna and G. Satyanarayana, RSC Adv., 2014, 4, 26662 DOI: 10.1039/C4RA04763J

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