期刊
ADVANCED SYNTHESIS & CATALYSIS
卷 363, 期 3, 页码 730-736出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/adsc.202000986
关键词
cyclization; cobalt catalysis; photoredox catalysis; semi-hydrogenation; 2,3-dihydrobenzofuran
资金
- National Natural Science Foundation of China [21676131, 21462019]
- Science Foundation of Jiangxi Province [20143ACB20012, 20202BAB213003]
- Education Department of Jiangxi Province [GJJ190616]
- Jiangxi Science & Technology Normal University [2018BSQD024]
- (Doctor Startup Fund)
A novel hydroxyl assisted, photoredox/cobalt co-catalyzed semi-hydrogenation and tandem cyclization reaction has been developed for the direct assembly of 2,3-dihydrobenzofurans, with moderate to good yields obtained for a variety of 2-propynolphenols under mild conditions. Mechanistic studies revealed the essential role of the alcoholic hydroxyl group and proposed a key low-valent cobalt catalyzed intramolecular hydroetherification of alkene.
Herein, a hydroxyl assisted, photoredox/cobalt co-catalyzed semi-hydrogenation and tandem cyclization of o-alkynylphenols is developed towards direct assembly of 2,3-dihydrobenzofurans. Moderate to good yields were obtained for a range of sterically and electronically diverse 2-propynolphenols under mild conditions. Mechanistic studies demonstrated the inevitable role of the alcoholic hydroxyl group with (Z)-alkene as the real intermediate. Finally, a key low-valent cobalt catalyzed intramolecular hydroetherification of alkene is proposed.
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