Synthesis of trifluoromethylated compounds with four consecutive asymmetric centers via sequential [3,3]-Ireland-Claisen rearrangement and iodolactonization-Reference-Cited by-同舟云学术

Synthesis of trifluoromethylated compounds with four consecutive asymmetric centers via sequential [3,3]-Ireland-Claisen rearrangement and iodolactonization

Published:1997-01 Issue:2 Volume:8 Page:223-230
ISSN:0957-4166
Container-title:Tetrahedron: Asymmetry
language:en
Short-container-title:Tetrahedron: Asymmetry

Author:

Konno Tsutomu,Kitazume Tomoya

Publisher

Elsevier BV

Subject

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

Reference21 articles.

1. Stereoselective Synthesis of Trifluoromethylated Compounds with Controlled Adjacent Tertiary Carbons by Michael Addition to (E)-3-(Trifluoromethyl)acrylates

2. Highly Diastereoselective Sequential Enolate-Michael Addition-Ireland Claisen Rearrangement

3. Highly Diastereoselective Michael Addition Reactions of Lithium Enolates to Ethyl 3-Trifluoromethylacrylate

4. Stereoselective Michael Addition Reactions of Acylated Oxazolidinones to Ethyl 3-Trifluoromethylacrylate

5. Synthesis of 3-Deoxy-3-C-Trifluoromethyl-d-Ribose Fromd-Xylose ord-Glucose

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