Issue 85, 2017
From the journal:

RSC Advances

Metal-free direct thiocarbamation of imidazopyridines with carbamoyl chloride and elemental sulfur†

Jian-Chao Deng,‡ab   Shi-Bin Zhuang,‡ab   Quan-Zhu Liu,ab   Zi-Wei Lin,ab   Yu-Liang Su,ab   Jia-Hao Chenab  and  Ri-Yuan Tang ORCID logo *ab  

* Corresponding authors

a Department of Applied Chemistry, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China
E-mail: rytang@scau.edu.cn

b Key Laboratory of Natural Pesticide & Chemical Biology, Ministry of Education, South China Agricultural University, Guangzhou 510642, China

Abstract

The combination of elemental sulfur and carbamoyl chloride was found to act as a carbamothioyl group surrogate for direct thiocarbamation of imidazopyridines in the absence of a metal catalyst.

Graphical abstract: Metal-free direct thiocarbamation of imidazopyridines with carbamoyl chloride and elemental sulfur

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C7RA10819B
Article type
Paper
Submitted
30 Sep 2017
Accepted
18 Nov 2017
First published
23 Nov 2017
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2017,7, 54013-54016

Permissions

Request permissions

Metal-free direct thiocarbamation of imidazopyridines with carbamoyl chloride and elemental sulfur

J. Deng, S. Zhuang, Q. Liu, Z. Lin, Y. Su, J. Chen and R. Tang, RSC Adv., 2017, 7, 54013 DOI: 10.1039/C7RA10819B

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, 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 commercial 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