Jump to main content
Jump to site search

Issue 5, 2014
Previous Article Next Article

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

Author affiliations

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

Back to tab navigation

Supplementary files

Publication details

The article was received on 30 Sep 2013, accepted on 18 Nov 2013 and first published on 19 Nov 2013


Article type: Communication
DOI: 10.1039/C3OB41974F
Org. Biomol. Chem., 2014,12, 728-731

  •   Request permissions

    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

Search articles by author

Spotlight

Advertisements