Stereoselective Transformations of α-Trifluoromethylated Ketoximes to Optically Active Amines by Enzyme-Nanometal Cocatalysis: Synthesis of (S)-Inhibitor of Phenylethanolamine N-Methyltransferase-Reference-Cited by-同舟云学术

Stereoselective Transformations of α-Trifluoromethylated Ketoximes to Optically Active Amines by Enzyme-Nanometal Cocatalysis: Synthesis of (S)-Inhibitor of Phenylethanolamine N-Methyltransferase

Published:2014-05-30 Issue:7 Volume:6 Page:2129-2133
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Cheng Guilin,Wu Qi,Shang Zeyu,Liang Xinhua,Lin Xianfu

Publisher

Wiley

Subject

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

Reference41 articles.

1. Asymmetric Synthesis of Trifluoromethylated Allylic Amines Using α,β-Unsaturated N-tert-Butanesulfinimines

2. Asymmetric synthesis of either diastereomer of trifluoromethylated allylic amines by the selective reduction of trifluoromethyl α,β-unsaturated N-tert-butanesulfinyl ketoimines

3. Synthesis of fluorinated chiral amines using N-tert-butylsulfinyl imines

4. Highly diastereoselective synthesis of α-trifluoromethylated α-propargylamines by acetylide addition to chiral CF3-substituted N-tert-butanesulfinyl ketimines

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