期刊
CHEMICAL COMMUNICATIONS
卷 55, 期 54, 页码 7808-7811出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9cc03604k
关键词
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资金
- National Natural Science Foundation of China [21772137, 21542015, 21672157]
- PAPD
- Project of Scientific and Technological Infrastructure of Suzhou [SZS201708]
- Major Basic Research Project of the Natural Science Foundation of the Jiangsu Higher Education Institutions [16KJA150002]
- Soochow University
Cascade cyclization reactions of S(3)(-)in situ generated from S-2(-) with 1,3-enynes for the chemoselective synthesis of 2,3,5-trisubstituted thiophenes and 3-thienyl disulfides controlled by sulfide salts are developed. These two protocols provide new, environment-friendly and simple strategies to construct 2,3,5-trisubstituted thiophenes and 3-thienyl disulfides via the formation of two and six C-S bonds, respectively.
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