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Issue 5, 2014
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Synthesis of substituted indenones and indanones by a Suzuki–Miyaura coupling/acid-promoted cyclisation sequence

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Abstract

A one-pot Suzuki–Miyaura cross-coupling/acid-catalyzed cyclisation leading to indenones and indanones in modest to good yields is reported.

Graphical abstract: Synthesis of substituted indenones and indanones by a Suzuki–Miyaura coupling/acid-promoted cyclisation sequence

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Supplementary files

Article information


Submitted
30 Sep 2013
Accepted
18 Nov 2013
First published
19 Nov 2013

Org. Biomol. Chem., 2014,12, 728-731
Article type
Communication

Synthesis of substituted indenones and indanones by a Suzuki–Miyaura coupling/acid-promoted cyclisation sequence

A. N. Butkevich, B. Ranieri, L. Meerpoel, I. Stansfield, P. Angibaud, A. Corbu and J. Cossy, Org. Biomol. Chem., 2014, 12, 728
DOI: 10.1039/C3OB41974F

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