Reaction des hexadiene-1,5 ols-3 avec le trifluoroacetate mercurique ; transposition d'oxy-cope a temperature ambiante.-Reference-Cited by-同舟云学术

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Reaction des hexadiene-1,5 ols-3 avec le trifluoroacetate mercurique ; transposition d'oxy-cope a temperature ambiante.

Published:1982-01 Issue:41 Volume:23 Page:4263-4266
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Bluthe Norbert,Malacria Max,Gore Jacques

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Effect of solvent on the oxy–Cope rearrangement of the 4-isopropenyl-3,7-dimethylocata-1,6-dien-3-ol diastereomeric system

2. A New Efficient Synthesis of Polyprenyl Ketones via Oxy-Cope Rearrangement

3. New sigmatropic sequences based on the [2,3] Wittig rearrangement of bis(allylic) ethers. Regiocontrolled joining reactions of two or three allylic moieties leading to unsaturated carbonyl compounds

4. Vinylallenes—V(xf†)

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1. Gold‐Catalyzed Arylative Cope Rearrangement;Angewandte Chemie International Edition;2024-06-30

2. Gold‐Catalyzed Arylative Cope Rearrangement;Angewandte Chemie;2024-06-30

3. Formation of Aldehydes and Ketones by Rearrangements;Comprehensive Organic Transformations;2018-02-28

4. Mercury(II) Trifluoroacetate;Fieser and Fieser's Reagents for Organic Synthesis;2011-08-15

5. Mercury(II) Trifluoroacetate;Fieser and Fieser's Reagents for Organic Synthesis;2009-12-15

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