A new synthesis of monosubstituted succinaldehydes and 3-substituted pyrroles from acetonitriles. Formal synthesis of 2,3-dihydro-7-methyl-2H-pyrrolizidin-1-one (Danaidone), a semiochemical of danaid butterflies-Reference-Cited by-同舟云学术

A new synthesis of monosubstituted succinaldehydes and 3-substituted pyrroles from acetonitriles. Formal synthesis of 2,3-dihydro-7-methyl-2H-pyrrolizidin-1-one (Danaidone), a semiochemical of danaid butterflies

Published:1996-06 Issue:24 Volume:37 Page:4099-4102
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Méndez Jose Manuel,Flores Blas,León Fernando,Martínez María Eugenia,Vázquez Alfredo,García Gustavo Alberto,Salmón Manuel

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference19 articles.

1. Syntheses of 3-substituted pyrrole derivatives with antiinflammatory activity.

2. Evidence for monomeric metaphosphate as an intermediate in the hydrolysis of .mu.-monothiopyrophosphate

3. Route to chemically modified chiral electrodes: synthesis and properties of optically active pyrrole monomers

4. Observation of the cation radicals of pyrrole and of some substituted pyrroles in fast-scan cyclic voltammetry. Standard potentials and lifetimes

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