Issue 7, 1972

Benzoheterocycles via aryne C–C cyclisation: 2-methylisoindole

Abstract

2-Methylisoindole is obtained in high yield by the reaction of N-methyl-2-chlorobenzylaminoacetonitrile with potassamide in liquid ammonia.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 397-397

Benzoheterocycles via aryne C–C cyclisation: 2-methylisoindole

B. Jaques and R. G. Wallace, J. Chem. Soc., Chem. Commun., 1972, 397 DOI: 10.1039/C39720000397

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