Issue 53, 2015
From the journal:

RSC Advances

Substrate selective synthesis of pyrazolo[1,5-a]pyridines through [3 + 2] cycloaddition of N-aminopyridines and β-nitro styrenes†

Chitrakar Ravi,a   Darapaneni Chandra Mohan,a   N. Naresh Kumar Reddya  and  Subbarayappa Adimurthy*a  

* Corresponding authors

a Academy of Scientific & Innovative Research, CSIR – Central Salt & Marine Chemicals Research Institute, G. B. Marg, Bhavnagar-364 002, Gujarat, India
E-mail: adimurthy@csmcri.org

Abstract

Synthesis of (hetero)aryl pyrazolo[1,5-a]pyridines through [3 + 2] cycloaddition of N-aminopyridine with β-nitrostyrenes followed by in situ denitration and oxidation under metal-free, mild conditions are described.

Graphical abstract: Substrate selective synthesis of pyrazolo[1,5-a]pyridines through [3 + 2] cycloaddition of N-aminopyridines and β-nitro styrenes

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C5RA06707C
Article type
Communication
Submitted
26 Mar 2015
Accepted
22 Apr 2015
First published
23 Apr 2015

RSC Adv., 2015,5, 42961-42964

Permissions

Request permissions

Substrate selective synthesis of pyrazolo[1,5-a]pyridines through [3 + 2] cycloaddition of N-aminopyridines and β-nitro styrenes

C. Ravi, D. Chandra Mohan, N. Naresh Kumar Reddy and S. Adimurthy, RSC Adv., 2015, 5, 42961 DOI: 10.1039/C5RA06707C

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