期刊
ASIAN JOURNAL OF ORGANIC CHEMISTRY
卷 7, 期 4, 页码 720-723出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.201800030
关键词
alkenes; difunctionalization; electrophilic reaction; selenoamidation; beta-amidoselenides
资金
- National Natural Science Foundation of China [U1504210]
- Program for Innovative Research Team of Science and Technology in the University of Henan Province [18IRTSTHN004]
- Jilin Province Key Laboratory of Organic Functional Molecular Design Synthesis [130028743]
- [aynu201708]
An eco-friendly method has been developed for the 1,2-selenoamidation of alkenes under metal-free conditions. The reaction avoids the need for pre-prepared Se-N regents, providing facile access to a variety of beta-amidoselenides with good regioselectivity and functional group tolerance. The broad substrate scope, good regioselectivity and easy derivation make this reaction attractive for the synthesis of nitrogen- and selenium-containing molecules.
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