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Volumn , Issue 28, 2007, Pages 2977-2979

Evolution of chiral Lewis basic N-formamide as highly effective organocatalyst for asymmetric reduction of both ketones and ketimines with an unprecedented substrate scope

(4) Zhou, Li a,c Wang, Zhouyu a,b,c Wei, Siyu a Sun, Jian a

a CHENGDU INSTITUTE OF BIOLOGY (China)

b XIHUA UNIVERSITY (China)

c UNIVERSITY OF CHINESE ACADEMY OF SCIENCES (China)

Author keywords

[No Author keywords available]

Indexed keywords

FORMAMIDE; IMINE; KETONE; LEWIS BASE; PIPECOLIC ACID;

ARTICLE; CATALYST; CHIRALITY; DIASTEREOISOMER; ENANTIOSELECTIVITY; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; HYDROSILYLATION; REDUCTION KINETICS; TEMPERATURE DEPENDENCE;

EID: 34447331272 PISSN: 13597345 EISSN: None Source Type: Journal
DOI: 10.1039/b703307a Document Type: Article

Times cited : (74)

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