Enantioselective synthesis of quaternary stereogenic centers through catalytic asymmetric addition of dimethylzinc to α-ketoesters with chiral cis-cyclopropane-based amide alcohol as ligand-Reference-Cited by-同舟云学术

Enantioselective synthesis of quaternary stereogenic centers through catalytic asymmetric addition of dimethylzinc to α-ketoesters with chiral cis-cyclopropane-based amide alcohol as ligand

Published:2009-09 Issue:18 Volume:20 Page:2125-2129
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Zheng Bing,Hou Shicong,Li Zhiyuan,Guo Hongchao,Zhong Jiangchun,Wang Min

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. Concise and Practical Synthesis of C-Glycosyl Ketones from Sugar Benzothiazoles and Their Transformation into Chiral Tertiary Alcohols

2. A New Stereoselective Route to Chiral Tertiary Alcohols in Water

3. Synthesis of Homoallylic Chiral Tertiary Alcohols via Chelation-Controlled Diastereoselective Nucleophilic Addition on α-Alkoxyketones: Application for the Synthesis of the C1−C11 Subunit of 8-epi-Fostriecin

4. Asymmetric alkynylzinc additions to aldehydes and ketones

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