Highly Enantioselective [3+2] Coupling of Indoles with Quinone Monoimines Promoted by a Chiral Phosphoric Acid | Zendy

Liao Lihua | Zendy; Shu Chang | Zendy; Zhang Minmin | Zendy; Liao Yijun | Zendy; Hu Xiaoyan | Zendy; Zhang Yonghong | Zendy; Wu Zhijun | Zendy; Yuan Weicheng | Zendy; Zhang Xiaomei | Zendy

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Highly Enantioselective [3+2] Coupling of Indoles with Quinone Monoimines Promoted by a Chiral Phosphoric Acid

Author(s) -

Liao Lihua,

Shu Chang,

Zhang Minmin,

Liao Yijun,

Hu Xiaoyan,

Zhang Yonghong,

Wu Zhijun,

Yuan Weicheng,

Zhang Xiaomei

Publication year - 2014

Publication title -

angewandte chemie international edition

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 5.831

H-Index - 550

eISSN - 1521-3773

pISSN - 1433-7851

DOI - 10.1002/anie.201405689

Subject(s) - enantioselective synthesis , phosphoric acid , quinone , chemistry , coupling (piping) , organic chemistry , combinatorial chemistry , catalysis , materials science , metallurgy

Highly enantioselective [3+2] coupling of 3‐substituted indoles with quinone monoimines promoted by a chiral phosphoric acid has been reported. A large variety of benzofuroindolines were prepared in moderate to good yields (up to 98 %) with generally excellent enantioselectivities (up to 99 % ee ).

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