From intermolecular alcohol additions on a double bond to electrocyclizations of non-activated γ, δ-unsaturated alcohols: An easy synthesis of tetrahydrofurans-Reference-Cited by-同舟云学术

From intermolecular alcohol additions on a double bond to electrocyclizations of non-activated γ, δ-unsaturated alcohols: An easy synthesis of tetrahydrofurans

Published:1997-02 Issue:8 Volume:38 Page:1413-1414
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Franck Xavier,Figadére Bruno,Cavé André

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference11 articles.

1. Synthetic routes to 2,5-disubstituted tetrahydrofurans

2. Ring Closure Reactions of Substituted 4-Pentenyl-1-oxy Radicals. The Stereoselective Synthesis of Functionalized Disubstituted Tetrahydrofurans

3. Advanced Organic Chemistry;March,1985

4. A facile and highly chemoselective protection of primary hydroxyl groups with 2-methyl-1-butene.

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