Chiral ligands derived from abrine. Part 7: Effect of O, S, N in aromatic ring substituents at C-1 on enantioselectivity induced by tetrahydro-β-carboline ligands in diethylzinc addition to aldehydes-Reference-Cited by-同舟云学术

Chiral ligands derived from abrine. Part 7: Effect of O, S, N in aromatic ring substituents at C-1 on enantioselectivity induced by tetrahydro-β-carboline ligands in diethylzinc addition to aldehydes

Published:2001-10 Issue:18 Volume:12 Page:2613-2619
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Zhu H.J.,Zhao B.T.,Zuo G.Y.,Pittman C.U.,Dai W.M.,Hao X.J.

Publisher

Elsevier BV

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Reference18 articles.

1. Enantioselective addition of diethylzinc to benzaldehyde catalyzed by a small amount of chiral 2-amino-1-alcohols

2. Catalytic asymmetric induction. Highly enantioselective addition of dialkylzincs to aldehydes

3. Enantioselective addition of organozinc reagents to aldehydes

4. First enantioselective addition of dialkylzinc to ketones promoted by titanium(IV) derivatives

5. Catalytic Asymmetric Addition of ZnPh2 to Ketones: Enantioselective Formation of Quaternary Stereocenters

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