1,3,4-Thiadiazoles and 1,3-thiazoles from one-pot reaction of bisthioureas with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate

Show full item record



Permalink

http://hdl.handle.net/10138/309243

Citation

Aly , A A , Hassan , A A , Bräse , S , Ibrahim , M A A , Abd Al-Latif , E-S S M , Spuling , E & Nieger , M 2017 , ' 1,3,4-Thiadiazoles and 1,3-thiazoles from one-pot reaction of bisthioureas with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate ' , Journal of Sulfur Chemistry , vol. 38 , no. 1 , pp. 69-75 . https://doi.org/10.1080/17415993.2016.1237637

Title: 1,3,4-Thiadiazoles and 1,3-thiazoles from one-pot reaction of bisthioureas with 2-(bis(methylthio)methylene)malononitrile and ethyl 2-cyano-3,3-bis(methylthio)acrylate
Author: Aly, Ashraf A.; Hassan, Alaa A.; Bräse, Stefan; Ibrahim, Mahmoud A. A.; Abd Al-Latif, El-Shimaa S. M.; Spuling, Eduard; Nieger, Martin
Contributor: University of Helsinki, Department of Chemistry
Date: 2017-02
Language: eng
Number of pages: 7
Belongs to series: Journal of Sulfur Chemistry
ISSN: 1741-5993
URI: http://hdl.handle.net/10138/309243
Abstract: Bisthioureas reacted with either 2-(bis(methylthio)methylene)malononitrile or ethyl 2-cyano-3,3-bis(methylthio)acrylate to give 1,3,4-thiadiazoles and 1,3-thiazoles. Only, the reactive allyl derivative of bisthioureas reacted with the bis(methylthio)methylene compounds to give 1,3-thiazoles. The mechanism was discussed. The structures of products were proved by MS, IR, NMR and elemental analyses and X-ray structure analysis. [GRAPHICS]
Subject: Bisthioureas
bis(methylthio)malononitrile
bis(methylthio)acrylate
1
3
4-thiadiazoles
3-thiazoles
X-ray
DERIVATIVES
116 Chemical sciences
Rights:


Files in this item

Total number of downloads: Loading...

Files Size Format View
Journal_of_Sulf ... t_GSRP_2016_0109Edited.pdf 990.1Kb PDF View/Open

This item appears in the following Collection(s)

Show full item record