Stereoselective construction of the 1,1,1-trifluoroisopropyl moiety by asymmetric hydrogenation of 2-(trifluoromethyl)allylic alcohols and its application to the synthesis of a trifluoromethylated amino diol-Reference-Cited by-同舟云学术

Stereoselective construction of the 1,1,1-trifluoroisopropyl moiety by asymmetric hydrogenation of 2-(trifluoromethyl)allylic alcohols and its application to the synthesis of a trifluoromethylated amino diol

Published:2007-11 Issue:48 Volume:63 Page:11965-11972
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Chen Qi,Qing Feng-Ling

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference46 articles.

1. Enantioselective Synthesis of an All-syn Four Vicinal Fluorine Motif

2. Construction of Asymmetric Fluorinated Carbon Centers

3. Enantioselective α-Fluorination of Carbonyl Compounds: Organocatalysis or Metal Catalysis?

4. How to Reach Stereogenic Trifluoromethylated Carbon? En Route to the “Grail” of the Asymmetric Trifluoromethylation Reaction

5. Fluorinated Carbonyl and Olefinic Compounds: Basic Character and Asymmetric Catalytic Reactions

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