Issue 18, 1990
From the journal:

Journal of the Chemical Society, Chemical Communications

Cycloaddition reactions of carbodiimides. The first example of an intramolecular Diels–Alder reaction of C[double bond, length half m-dash]C-conjugated carbodiimides

Pedro Molina,   Mateo Alajarín  and  Angel Vidal  

Abstract

An one-pot preparation of α-carbolines and quinindolines from conjugated carbodiimides based on a tandem Intramolecular Diels–Alder cycloaddition/oxidative aromatization is described.

About
Cited by
Related
Download options Please wait...

Article information

DOI
https://doi.org/10.1039/C39900001277
Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 1277-1279

Permissions

Request permissions

Cycloaddition reactions of carbodiimides. The first example of an intramolecular Diels–Alder reaction of C[double bond, length half m-dash]C-conjugated carbodiimides

P. Molina, M. Alajarín and A. Vidal, J. Chem. Soc., Chem. Commun., 1990, 1277 DOI: 10.1039/C39900001277

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