Issue 22, 1995
From the journal:

Journal of the Chemical Society, Chemical Communications

Lewis acid catalysed cyclisation and halogen exchange reactions of 1,1′-biphenyl-2-yl isocyanide dihalides

Kevin S. Currie  and  George Tennant  

Abstract

1,1′-Biphenyl-2-yl isocyanide dichloride and dibromide undergo unprecedented intramolecular Friedel–Crafts type cyclisation reactions catalysed by various Lewis acids affording useful synthetic methods for otherwise difficult to access 6-chloro- and 6-bromo-phenanthridines; nucleophilic displacement reactions of the latter and halogen exchange reactions of 1,1′-biphenyl-2-yl isocyanide dichloride and dibromide are also described.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39950002295
Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2295-2296

Permissions

Request permissions

Lewis acid catalysed cyclisation and halogen exchange reactions of 1,1′-biphenyl-2-yl isocyanide dihalides

K. S. Currie and G. Tennant, J. Chem. Soc., Chem. Commun., 1995, 2295 DOI: 10.1039/C39950002295

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