Synthesis of enol ethers from lactones using modified Julia olefination reagents: application to the preparation of tri- and tetrasubstituted exoglycals-Reference-Cited by-同舟云学术

Synthesis of enol ethers from lactones using modified Julia olefination reagents: application to the preparation of tri- and tetrasubstituted exoglycals

Published:2008-01 Issue:5 Volume:49 Page:747-749
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bourdon Benjamin,Corbet Matthieu,Fontaine Patrice,Goekjian Peter G.,Gueyrard David

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference27 articles.

1. Olefin homologation with titanium methylene compounds

2. Titanium carbenoid reagents for converting carbonyl groups into alkenes

3. Cyanomethylenetrimethylphosphorane, a powerful reagent for the Wittig olefination of esters, lactones and imides

4. Synthesis and Uses of exo-Glycals

5. Synthesis and spontaneous dimerization of the tri-O-benzyl derivative of ”2-keto-1-C-methylene-d-glucopyranose” (2,6-anhydro-4,5,7-tri-O-benzyl-1-deoxy-d-arabino-hept-1-en-3-ulose)

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