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Angewandte Chemie - International Edition

Volumn 53, Issue 39, 2014, Pages 10471-10475

Highly enantioselective [3+2] coupling of indoles with quinone monoimines promoted by a chiral phosphoric acid

(9) Liao, Lihua a,b Shu, Chang a,b Zhang, Minmin a,b Liao, Yijun a,b Hu, Xiaoyan a,b Zhang, Yonghong a,b Wu, Zhijun c Yuan, Weicheng a Zhang, Xiaomei a

a CHENGDU INSTITUTE OF ORGANIC CHEMISTRY (China)

b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES (China)

c CHENGDU INSTITUTE OF BIOLOGY (China)

Author keywords

asymmetric catalysis; enantioselectivity; heterocycles; indoles; organocatalysis

Indexed keywords

CATALYSIS; PHOSPHORIC ACID;

ASYMMETRIC CATALYSIS; ENANTIOSELECTIVE; HETEROCYCLES; INDOLES; ORGANOCATALYSIS;

ENANTIOSELECTIVITY;

IMINE; INDOLE DERIVATIVE; PHOSPHORIC ACID; QUINONE DERIVATIVE;

CATALYSIS; CHEMISTRY; CONFORMATION; CYCLOADDITION; STEREOISOMERISM; SYNTHESIS; X RAY CRYSTALLOGRAPHY;

CATALYSIS; CRYSTALLOGRAPHY, X-RAY; CYCLOADDITION REACTION; IMINES; INDOLES; MOLECULAR CONFORMATION; PHOSPHORIC ACIDS; QUINONES; STEREOISOMERISM;

EID: 84908546559 PISSN: 14337851 EISSN: 15213773 Source Type: Journal
DOI: 10.1002/anie.201405689 Document Type: Article

Times cited : (138)

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- CCDC 1002543 (3 b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via
- CCDC 1002543 (3 b) contains the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.

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