Palladium‐Catalyzed Cross‐Coupling of Aryl Thioacetates and Chloro(hetero)arenes. Issue 2 (24th January 2020)

• Record Type: Journal Article
• Authors: Zhao, Tan; Liang, Feng; Cai, Mingjun; Chen, Junling; Kang, Chuanqing; Wang, Hongda; Wu, Qiang
• Is Part Of: Asian journal of organic chemistry. Volume 9:Issue 2(2020)
• Page Start: 214
• Page End: 217
• Publication Date: 2020-01-24
• Subjects: transition metals -- cross-coupling -- C−S bond formation -- chloro(hetero)arenes -- palladium; Chemistry, Organic -- Periodicals; Organic compounds -- Synthesis -- Periodicals; 547.005
• DOI: 10.1002/ajoc.202000025
• Languages: English
• ISSNs: 2193-5807

Abstract

Abstract: A simple and effective method for palladium‐catalyzed carbon‐sulfur bond formation was established with aryl thioacetates and chloro(hetero)arenes as starting materials. A wide range of thioacetates and chloro(hetero)arenes can be employed for the preparation of aryl sulfides in good to excellent yield. Abstract : C−S bonds : A simple and effective palladium catalyzed C–S bond formation with thioacetates and chloro(hetero)arenes has been developed. A broad variety of substrates were well converted to respective aryl sulfides in good to excellent yield.