期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 -, 期 -, 页码 -出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ange.202209625
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资金
- National Natural Science Foundation of China [22188101, 21871145]
- Haihe Laboratory of Sustainable Chemical Transformations and Frontiers Science Center for New Organic Matter, Nankai University [63181206]
- Fundamental Research Funds for the Central Universities
- Key Scientific Research Project in Colleges and Universities of Henan Province of China [22A150047]
Enantioselective Ni-catalyzed C(sp(3))-H bond activation was achieved using a phosphine oxide-ligated Ni-Al bimetallic catalyst, leading to the synthesis of a series of chiral N-containing heterocycles in good yields and high enantioselectivity.
Enantioselective Ni-catalyzed C(sp(3))-H bond activation remains an elusive challenge. Herein, we used phosphine oxide-ligated Ni-Al bimetallic catalyst to realize enantioselective Ni-catalyzed aliphatic C(sp(3))-H activation of formamides, providing a series of chiral N-containing heterocycles in 40-95 % yield and 70-95 % ee.
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