Issue 3, 1990

Preparation of tetrahydrobenz[cd]indoles from 1-tetralones

Abstract

3,4-Bridged indoles (5) are prepared from readily available aromatic ketones (1) by conversion into the epoxides (2), ring opening with azide ion to give the azido alcohols (3), dehydration, and thermolysis of the resulting vinyl azides (4).

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 689-693

Preparation of tetrahydrobenz[cd]indoles from 1-tetralones

A. L. Beck, W. J. Coates and C. J. Moody, J. Chem. Soc., Perkin Trans. 1, 1990, 689 DOI: 10.1039/P19900000689

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