Issue 63, 2014
From the journal:

RSC Advances

One-pot synthesis of new derivatives of pyran using N-halosulfonamide†

Ramin Ghorbani-Vaghei,*a   Zahra Salimi,a   Seyedeh Mina Malaekehpoor,a   Fatemeh Eslamia  and  Samira Nooria  

* Corresponding authors

a Department of Organic Chemistry, Faculty of Chemistry, Bu-Ali-Sina University, Hamedan, Iran
E-mail: rgvaghei@yahoo.com
Fax: +988118380709

Abstract

In this study N,N,N′,N′-tetrabromobenzene-1,3-disulfonamide was used as a reagent for the three-component one-pot synthesis of some novel 9-aryl-9H-2,4,5,7-tetramethyl-diuracilopyrans, which has not been published before, as well as 9-aryl-3,4,6,7-tetrahydro-2H-pyran-1,8(5H,9H)-diones in excellent yields. This is obtained from the condensation of aromatic and heterocyclic aldehydes and N,N-dimethylbarbituric acid or cyclohexane-1,3-diones in ethanol at room temperature.

Graphical abstract: One-pot synthesis of new derivatives of pyran using N-halosulfonamide

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C4RA04929B
Article type
Paper
Submitted
25 May 2014
Accepted
28 Jul 2014
First published
28 Jul 2014

RSC Adv., 2014,4, 33582-33586

Permissions

Request permissions

One-pot synthesis of new derivatives of pyran using N-halosulfonamide

R. Ghorbani-Vaghei, Z. Salimi, S. M. Malaekehpoor, F. Eslami and S. Noori, RSC Adv., 2014, 4, 33582 DOI: 10.1039/C4RA04929B

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