Catalytic Highly Enantioselective Alkylation of Aldehydes with Deactivated Grignard Reagents and Synthesis of Bioactive Intermediate Secondary Arylpropanols-Reference-Cited by-同舟云学术

Catalytic Highly Enantioselective Alkylation of Aldehydes with Deactivated Grignard Reagents and Synthesis of Bioactive Intermediate Secondary Arylpropanols

Published:2010-09-13 Issue:20 Volume:75 Page:6869-6878
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Liu Yi¹,Da Chao-Shan¹²,Yu Sheng-Li¹,Yin Xiao-Gang¹,Wang Jun-Rui¹,Fan Xin-Yuan¹,Li Wei-Ping³,Wang Rui¹

Affiliation:

1. Institute of Biochemistry & Molecular Biology, School of Life Sciences

2. State Key Laboratory of Applied Organic Chemistry

3. Department of Biology, Shantou University, Shantou 515063, People's Republic of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo101351t

Reference108 articles.

1. Catalytic Asymmetric Organozinc Additions to Carbonyl Compounds

2. Novel non-azacyclo 1,2-aminoalcohols derived from l-Phe and highly enantioselective addition of diethylzinc to aryl aldehydes

3. A convenient synthesis of piperidine-based β-amino alcohols from l-Phe and highly enantioselective addition of diethyl zinc to aldehydes

4. An Amino Alcohol Ligand for Highly Enantioselective Addition of Organozinc Reagents to Aldehydes: Serendipity Rules

5. Substrate Dependence of Nonlinear Effects: Mechanistic Probe and Practical Applications

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