期刊
CHEMICAL SCIENCE
卷 11, 期 41, 页码 11307-11314出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0sc03409f
关键词
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资金
- NIH [R35GM125052-03, R35GM128779]
- China Scholarship Council
- NSF [DGE-1346837]
- Life Science Summer Institute
- Bristol-Myers Squibb
- National Science Foundation [ACI-1548562]
We report a series of palladium(ii)-catalyzed, intramolecular alkene hydrofunctionalization reactions with carbon, nitrogen, and oxygen nucleophiles to form five- and six-membered carbo- and heterocycles. In these reactions, the presence of a proximal bidentate directing group controls the cyclization pathway, dictating the ring size that is generated, even in cases that are disfavored based on Baldwin's rules and in cases where there is an inherent preference for an alternative pathway. DFT studies shed light on the origins of pathway selectivity in these processes.
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