65236-05-7Relevant articles and documents
Synthesis of carbamothioate derivatives via a copper catalyzed thiocarboxamidation of aryl iodides
Khalaj, Mehdi
, p. 945 - 952 (2020/05/26)
Abstract: A catalytic route to carbamothioate derivatives through a reaction involving isocyanides, elemental sulfur, and aryl iodides has been developed. The reaction scope has been examined using a range of isocyanides and aryl iodides. The reactions involve two consecutive C–S bond formations. Control experiment revealed that the reaction proceeds through an iminium species. Graphic abstract: [Figure not available: see fulltext.].
Molecular iodine-mediated synthesis of thiocarbamates from thiols, isocyanides and water under metal-free conditions
Bao, Wen-Hu,Wu, Chao,Wang, Jing-Ting,Xia, Wen,Chen, Ping,Tang, Zilong,Xu, Xinhua,He, Wei-Min
supporting information, p. 7025 - 7029 (2018/10/02)
A simple and practical molecular iodine-mediated method for the efficient construction of thiocarbamates from isocyanides, thiols and water under metal-free and mild conditions has been developed. A variety of thiocarbamates were easily synthesized through this methodology, which has the advantages of simple operation, eco-friendly conditions, good functional group tolerance, and readily accessible raw materials.
Method of controlling pea aphids
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, (2008/06/13)
Novel S-aryl N-cycloalkylthiolcarbamates, such as S-4-methoxy-phenyl N-cyclohexylthiolcarbamate, which are useful for controlling pea aphids, and the method of controlling pea aphids with the compounds are disclosed.