[2,3]-Wittig rearrangement of γ-allyloxy-β-ketoesters. A new access to tetronic acids-Reference-Cited by-同舟云学术

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[2,3]-Wittig rearrangement of γ-allyloxy-β-ketoesters. A new access to tetronic acids

Published:2001-07 Issue:31 Volume:42 Page:5215-5218
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Pévet Isabelle,Meyer Christophe,Cossy Janine

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference43 articles.

1. Stereoselective synthesis of biologically active tetronic acids

2. A Convenient Synthesis of Optically Active 5,5-Disubstituted 4-Amino- and 4-Hydroxy-2(5H)-furanones from (S)-Ketone Cyanohydrins

3. Preparation of Chiral Lactones from L-Lactic Acid via (S)-gamma-Methyltetronic Acid.

4. Stereocontrolled synthesis of (3,4,5)-3-alkyl-4-hydroxy-5-methyl-2(3)-dihydrofubanones and derivatives

5. Total asymmetric syntheses of (+)-blastmycinone and related γ-lactones

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5. SOLVENT EFFECTS ON THE KETO-ENOL TAUTOMERIC EQUILIBRIUM OF TETRONIC AND ETHYL ACETOACETATE CARBON ACIDS: A THEORETICAL STUDY;Journal of Theoretical and Computational Chemistry;2010-12

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