Stereoselective formation of α-fluoro-α-trifluoromethyl-γ-lactones starting from γ-hydroxy-α,β-unsaturated sulfones and a hexafluoropropene-diethylamine adduct (PPDA)-Reference-Cited by-同舟云学术

Stereoselective formation of α-fluoro-α-trifluoromethyl-γ-lactones starting from γ-hydroxy-α,β-unsaturated sulfones and a hexafluoropropene-diethylamine adduct (PPDA)

Published:1997-07 Issue:29 Volume:38 Page:5173-5176
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ogura Katsuyuki,Ogu Ken-ichi,Ayabe Takashi,Sonehara Jun-ichi,Akazome Motohiro

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference17 articles.

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2. Synthesis of chiral and bioactive fluoroorganic compounds

3. Novel Ferroelectricity in Fluorinated Ferroelectric Liquid Crystal

4. Effect of Core Structure on Spontaneous Polarization in New Ferroelectric Liquid Crystals with a Fluorinated Chiral Part

5. Synthesis of trifluoromethyl-containing monomers for the preparation of piezoelectric polymers

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2. Unprecedented 3- O -methyl-3- C -trifluoromethyl- d -ribono- (and l -lyxono)-γ-lactones synthesized by nucleophilic trifluoromethylation of d -hexose-derived cyclic ketones;Journal of Fluorine Chemistry;2016-06

3. ChemInform Abstract: Stereoselective Formation of α-Fluoro-α-trifluoromethyl-. gamma.-lactones Starting from γ-Hydroxy-α,β- Unsaturated Sulfones and a Hexafluoropropene-Diethylamine Adduct (PPDA) .;ChemInform;2010-08-03

4. 1,1,2,3,3,3-Hexafluoropropene;Encyclopedia of Reagents for Organic Synthesis;2009-03-15

5. Diethyl(1,1,2,3,3,3-hexafluoropropyl)amine;Encyclopedia of Reagents for Organic Synthesis;2007-03-15