A general strategy for the synthesis of 2,2′-, 2,3′-, and 2,7′-bi-indolyls

David St. C. Black; Naresh Kumar

doi:10.1039/C39840000441

You do not have JavaScript enabled. Please enable JavaScript to access the full features of the site or access our non-JavaScript page.

A general strategy for the synthesis of 2,2′-, 2,3′-, and 2,7′-bi-indolyls

David St. C. Black and Naresh Kumar

Abstract

Various substituted indoles undergo electrophilic substitution with indolin -2-one or 4,6-dimethoxyindolin-2-one and phosphoryl chloride to afford 2,2′-,2,3′-,or2,7′-bi-indolyls, depending on the initial substitution pattern.

Download options Please wait...

Article information

DOI: https://doi.org/10.1039/C39840000441
Article type: Paper

Download Citation

J. Chem. Soc., Chem. Commun., 1984, 441-442

Permissions

Request permissions

A general strategy for the synthesis of 2,2′-, 2,3′-, and 2,7′-bi-indolyls

D. St. C. Black and N. Kumar, J. Chem. Soc., Chem. Commun., 1984, 441 DOI: 10.1039/C39840000441

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.

Fetching data from CrossRef.
This may take some time to load.

Journal of the Chemical Society, Chemical Communications

A general strategy for the synthesis of 2,2′-, 2,3′-, and 2,7′-bi-indolyls

Abstract

Article information

Download Citation

Permissions

A general strategy for the synthesis of 2,2′-, 2,3′-, and 2,7′-bi-indolyls

Search articles by author

Spotlight

Advertisements