An Efficient Chan–Lam S‐Arylation of Arylthioureas with Arylboronic Acids

A convenient and efficient protocol has been developed for the preparation of aryl‐isothioureas based on the Chan–Lam C–S coupling reaction. The desired aryl‐isothioureas were synthesized in good yields (up to 95 %) in the presence of Cu(OAc)2·H2O as catalyst and bipyridine as ligand. A variety of f...

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Veröffentlicht in:European journal of organic chemistry 2018-08, Vol.2018 (32), p.4483-4489
Hauptverfasser: Liu, Xing, Zhang, Shi‐Bo, Zhu, Hui, Cheng, Yu, Peng, Han‐Ying, Dong, Zhi‐Bing
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Sprache:eng
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Zusammenfassung:A convenient and efficient protocol has been developed for the preparation of aryl‐isothioureas based on the Chan–Lam C–S coupling reaction. The desired aryl‐isothioureas were synthesized in good yields (up to 95 %) in the presence of Cu(OAc)2·H2O as catalyst and bipyridine as ligand. A variety of functional groups on the aryl‐thiourea and arylboronic acid reagents are tolerated. The method features mild reaction conditions and good yields, thereby illustrating its practical synthetic value in organic synthesis. A convenient and efficient protocol has been developed for the preparation of aryl‐isothioureas based on the Chan–Lam C–S coupling reaction. The desired aryl‐isothioureas were synthesized in good yields (up to 95 %) in the presence of Cu(OAc)2·H2O as catalyst and bipyridine as ligand.
ISSN:1434-193X
1099-0690
DOI:10.1002/ejoc.201800892