Stéréosélectivité comparée de la réduction de trifluorométhylcétones et des méthylcétones correspondantes: nouvelles voies d'accès à des dérivés trifluorométhylés de pentoses-Reference-Cited by-同舟云学术

Stéréosélectivité comparée de la réduction de trifluorométhylcétones et des méthylcétones correspondantes: nouvelles voies d'accès à des dérivés trifluorométhylés de pentoses

Published:1995-01 Issue:4 Volume:51 Page:1229-1244
ISSN:0040-4020
Container-title:Tetrahedron
language:fr
Short-container-title:Tetrahedron

Author:

Munier Pascal,Krusinski Aniela,Picq Dominique,Anker Daniel

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference44 articles.

1. Fluorinated Heterocycles: Targets in the Search for Bioactive Compounds and Tools for their Preparation

2. Synthesis of trifluoromethyl analogue of L-fucose and 6-deoxy-D-altrose

3. Trifluoromethylation of chiral aldehyde and synthesis of 6-deoxy-6,6,6-trifluorohexoses.

4. Chiral trifluoromethylated 2-butenolides for the construction of 6-deoxy-6,6,6-trifluorosugars

5. Trifluoromethylation of sugar 1,4-lactones : Synthesis of 5-deoxy-5,5,5-trifluoro-D and L-ribose and lyxose derivatives

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