Issue 0, 1984

Regio- and stereo-chemical aspects of [2 + 2] photocycloaddition between 1-benzoylindoles and olefins

Abstract

The regio- and stereo-selectivities in the [2 + 2] photocycloaddition of a series of 1-benzoylindoles with vinyl acetate and methyl acrylate have been investigated. With some exceptions, the 1 -benzoylindoles gave exclusively or predominantly the corresponding 1-acetoxy-3-benzoyl and 3-benzoyl-1-methoxycarbonyl-1,2,2a,7b-tetrahydro-3H-cyclobut[b]indoles as mixtures of stereoisomers.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1984, 405-412

Regio- and stereo-chemical aspects of [2 + 2] photocycloaddition between 1-benzoylindoles and olefins

M. Ikeda, K. Ohno, S. Mohri, M. Takahashi and Y. Tamura, J. Chem. Soc., Perkin Trans. 1, 1984, 405 DOI: 10.1039/P19840000405

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements