Development of highly enantioselective new Lewis basic N-formamide organocatalysts for hydrosilylation of imines with an unprecedented substrate profile

Tetrahedron

Volumn 64, Issue 49, 2008, Pages 11304-11312

  Wu, Pengcheng ^a   Wang, Zhouyu ^a,b   Cheng, Mounuo ^a   Zhou, Li ^a   Sun, Jian ^a  

^a CHENGDU INSTITUTE OF BIOLOGY   (China)

^b XIHUA UNIVERSITY   (China)

Author keywords

Acyclic ketimines; Asymmetric reduction; l Pipecolinic acid; Lewis basic organocatalysts

Indexed keywords

FORMAMIDE; IMINE;

ARTICLE; CATALYST; CHEMICAL REACTION; CHEMICAL STRUCTURE; ENANTIOSELECTIVITY; HYDROSILYLATION; OXIDATION REDUCTION REACTION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE;

EID: 54549102004     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2008.09.034     Document Type: Article

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