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Issue 51, 2014
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An efficient synthesis of highly substituted indanones and chalcones promoted by superacid

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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

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Publication details

The article was received on 01 Apr 2014, accepted on 06 Jun 2014 and first published on 09 Jun 2014


Article type: Communication
DOI: 10.1039/C4RA04763J
Citation: RSC Adv., 2014,4, 26662-26666
  • Open access: Creative Commons BY-NC license
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    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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