期刊
ORGANIC & BIOMOLECULAR CHEMISTRY
卷 17, 期 18, 页码 4593-4599出版社
ROYAL SOC CHEMISTRY
DOI: 10.1039/c9ob00601j
关键词
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资金
- National Natural Sciences Foundation of China [21672032, 21802016]
Trifluoromethylation-triggered cyclization of alkenes provides a useful route to CF3-containing cyclic compounds. Current approaches to generate CF3-based initiators from a CF3 source require a catalyst or an activator. This work describes a catalyst-free protocol to innately produce electrophilic CF3 species from PhICF3Cl for trifluoromethylative cyclization of acryloanilides. A new domino biscyclization of dienes has been developed leading to trifluoroethylated tetrahydroindenoquinolinones with chemo-and stereoselectivity.
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