Asymmetric Synthesis of Novel Vicinal Amino Alcohols via Intramolecular Ketone-N-sulfinylimine Pinacol-Type Reductive Coupling Promoted by SmI2-Reference-Cited by-同舟云学术

Asymmetric Synthesis of Novel Vicinal Amino Alcohols via Intramolecular Ketone-N-sulfinylimine Pinacol-Type Reductive Coupling Promoted by SmI2

Published:2014-02-24 Issue:7 Volume:44 Page:1012-1018
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Zhao Yun-Hui¹,Liu Han-Wen¹

Affiliation:

1. a Key Laboratory of Theoretical Chemistry and Molecular Simulation of Ministry of Education, Hunan Province College Key Laboratory of QSAR/QSPR , Hunan University of Science and Technology , Xiangtan , China

Funder

The generous financial support from the National Natural Science Foundation of China (Nos. 2097104 and 20672135) and the National Natural Science Foundation of Hunan (11JJ3016) is gratefully acknowledged.

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2013.841938

Reference11 articles.

1. Large-Scale and Highly Enantioselective Synthesis of the Taxol C-13 Side Chain through Asymmetric Dihydroxylation

2. Synthesis and receptor binding of enantiomeric N-substituted cis-N-[2-(3,4-dichlorophenyl)ethyl]-2-(1-pyrrolidinyl)cyclohexylamines as high-affinity .sigma. receptor ligands

3. 1,2-Amino Alcohols and Their Heterocyclic Derivatives as Chiral Auxiliaries in Asymmetric Synthesis

4. Synthesis of tetrahydronaphthyl thioureas as potent appetite suppressants☆

5. Catalytic asymmetric synthesis of secondary alcohols using chiral cis-1-amino-2-hydroxy-1,2,3,4-tetrahydronaphthalene as chiral ligand

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