1987ChemInformRequires access

ChemInform Abstract: Synthesis of Enamine Esters.

Vyacheslav Ya. Sosnovskikh, I. S. Ovsyannikov, A. L. Nikol'skii

Open publisher page 0 citations

Abstract

Abstract In the presence of Et2NMgBr, which is formed by reacting Et2NH with EtMgBr, the enolized forms of the esters (II), which are stabilized by Et2NMgBr add to the aryl nitriles (I) to yield the title compounds (III) ‐ useful synthons for the preparation of heterocycles.

About this research paper

What this paper is about

Abstract In the presence of Et2NMgBr, which is formed by reacting Et2NH with EtMgBr, the enolized forms of the esters (II), which are stabilized by Et2NMgBr add to the aryl nitriles (I) to yield the title compounds (III) ‐ useful synthons for the preparation of heterocycles.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Abstract In the presence of Et2NMgBr, which is formed by reacting Et2NH with EtMgBr, the enolized forms of the esters (II), which are stabilized by Et2NMgBr add to the aryl nitriles (I) to yield the title compounds (III) ‐ useful synthons for the preparation of heterocycles.

Key concepts: Chemistry, Synthon, Enamine, Yield (engineering), Aryl, Organic chemistry, Combinatorial chemistry, Catalysis

Related papers

Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Synthesis of Enamine Esters. — Research Paper | ScholarLens