Unsaturated carboxylic acid dienolates. Michael addition to enones through tandem 1,2-addition - oxy-cope rearrangement.-Reference-Cited by-同舟云学术

Unsaturated carboxylic acid dienolates. Michael addition to enones through tandem 1,2-addition - oxy-cope rearrangement.

Published:1985-01 Issue:20 Volume:26 Page:2485-2488
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Ballester P.,García-Raso A.,Gómez-Solivellas A.,Mestres R.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference22 articles.

1. Synthesis of unsaturated 5-hydroxy- and 7-oxo-acids by addition of unsaturated carboxylic acid dienolates to carbonyl compounds

2. Generation of unsaturated carboxylic dienolates by the lithium naphtalenide-diethylamine system, as well as addition conditions and working up has been described in above references. See as well reference 6.

3. The Reactions of Dianions of Carboxylic Acids and Ester Enolates

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1. Internally Lewis acid-catalyzed Diels-Alder cycloadditions;Tetrahedron;1997-07

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4. 13C NMR studies of dianions of unsaturated carboxylic acids;Tetrahedron;1994-04

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