期刊
TETRAHEDRON
卷 73, 期 26, 页码 3702-3706出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2017.05.010
关键词
Nucleophilic disulfurating reagents; Unsymmetrical disulfides; Copper; Synthetic methods
资金
- NSFC [21672069, 21472050, 21272075]
- DFMEC [20130076110023]
- Fok Ying Tung Education Foundation [141011]
- Program for Shanghai Rising Star [15QA1401800]
- National Program for Support of Top-notch Young Professionals
- Special Appointment (Eastern Scholar) at Shanghai Institutions of Higher Learning
Novel disulfuration was established via cross coupling between nucleophilic disulfurating reagent and arylsilane introducing two sulfur atoms in one step. This methodology was applied to synthesize various unsymmetrical disulfides under mild conditions via copper-catalyzed oxidative Hiyama-type cross coupling, providing a new pathway for disulfide synthesis. In addition, pH value of system displayed a key role in alcoholysis process. (C) 2017 Elsevier Ltd. All rights reserved.
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