Author:
Komatsu Mitsuo,Shibata Jun-ichi,Ohshiro Yoshiki,Agawa Toshio
Publisher
The Chemical Society of Japan
Cited by
14 articles.
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1. Multicomponent reactions (MCRs) of arylmethyl bromides, arylamidines and elemental sulfur toward unsymmetric 3,5-diaryl 1,2,4-thiadiazoles;Tetrahedron Letters;2017-06
2. Highly Efficient Oxidative Dimerization of Thioamides to 3,5-Disubstituted 1,2,4-Thiadiazoles Mediated by DDQ;Synthetic Communications;2012-03-26
3. Optimizing thiadiazole analogues of resveratrol versus three chemopreventive targets;Bioorganic & Medicinal Chemistry;2012-01
4. Solvent-Free Synthesis of 3,5-di(Hetero)Aryl-1,2,4-Thiadiazoles by Grinding of Thioamides under Oxidative Conditions;Journal of Chemical Research;2010-03
5. IBX/TEAB-mediated oxidative dimerization of thioamides: synthesis of 3,5-disubstituted 1,2,4-thiadiazoles;Tetrahedron Letters;2009-10