Issue 12, 2010
From the journal:

Chemical Communications

Generation of azomethineimine and metal-free formal 1,3-dipolar cycloaddition of imine with PhIO: reaction, scope, and synthesis†

Dilip K. Maiti,*a   Nirbhik Chatterjee,a   Palash Pandita  and  Sandip K. Hotaa  

* Corresponding authors

a Department of Chemistry, University of Calcutta, University College of Science, 92, A. P. C. Road, Kolkata-700009, India
E-mail: maitidk@yahoo.com
Fax: +91-33-2351-9755
Tel: +91-33-2350-9937

Abstract

Generation of azomethine imine and its scope in regioselective 1,3-dipolar cycloaddition (DC) of imine with PhIO toward highly substituted Δ2-1,2,4-triazoline, 1,2,4-triazole, and their fused, chiral, and sugar-based analogues are demonstrated.

Graphical abstract: Generation of azomethine imine and metal-free formal 1,3-dipolar cycloaddition of imine with PhIO: reaction, scope, and synthesis

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/B924761K
Article type
Communication
Submitted
24 Nov 2009
Accepted
16 Jan 2010
First published
10 Feb 2010

Chem. Commun., 2010,46, 2022-2024

Permissions

Request permissions

Generation of azomethine imine and metal-free formal 1,3-dipolar cycloaddition of imine with PhIO: reaction, scope, and synthesis

D. K. Maiti, N. Chatterjee, P. Pandit and S. K. Hota, Chem. Commun., 2010, 46, 2022 DOI: 10.1039/B924761K

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.

Social activity

Spotlight

Advertisements