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

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 j...

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Bibliographic Details
Published in:RSC advances 2014-01, Vol.4 (51), p.26662-26666
Main Authors: Das, Amrita, Krishna Reddy, Alavala Gopi, Krishna, Jonnada, Satyanarayana, Gedu
Format: Article
Language:English
Subjects:
Acetophenone
Aromatic compounds
Bonding
Carbon-carbon composites
Condensing
Formations
Ketones
Synthesis
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Summary: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.
ISSN:2046-2069
2046-2069
DOI:10.1039/C4RA04763J