Synthesis of the racemic forms of carbon–carbon double bond locked analogues of strobilurins which are characterized by a 2-arylcyclopropane ring cis-substituted at C-1 by the methyl (E)-3-methoxypropenoate unit-Reference-Cited by-同舟云学术

Synthesis of the racemic forms of carbon–carbon double bond locked analogues of strobilurins which are characterized by a 2-arylcyclopropane ring cis-substituted at C-1 by the methyl (E)-3-methoxypropenoate unit

Published:2002-05 Issue:19 Volume:58 Page:3673-3680
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Carpita Adriano,Ribecai Arianna,Rossi Renzo,Stabile Paolo

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference35 articles.

1. Biologically Active Molecules;Anke,1989

2. The strobilurins, oudemansins, and myxothiazols, fungicidal derivatives of β-methoxyacrylic acid

3. Strobilurins: Evolution of a New Class of Active Substances

4. Pd/Cu Co-catalysed Cross-coupling Reactions of Methyl (Z)-2-Tributylstannyl-3-methoxypropenoate: a Method for Direct Introduction of the Agrochemically Important β-Methoxyacrylate Toxophore

5. New Efficient Procedures for Direct Introduction of the Agrochemically Important β-Methoxypropenoate Unit into Substituted Aromatic Derivatives

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