ScholarLens Back to search
1988•ChemInformRequires access

ChemInform Abstract: Chemistry of Aryl‐Lead(IV) Tricarboxylates. Reaction with Vinylogous β‐Keto Esters.

Darren J. Ackland, JT Pinhey

Open publisher page 0 citations

Abstract

Abstract Hagemann's ester (IIa) and the demethyl analogue (VI) (in equilibrium with the isomer (VII)) in Py/CHCl3 or in DMSO undergo regiospecific arylation at C‐1 with aryl‐lead triacetates (I) to yield (III) and (VIII), respectively.

About this research paper

What this paper is about

Abstract Hagemann's ester (IIa) and the demethyl analogue (VI) (in equilibrium with the isomer (VII)) in Py/CHCl3 or in DMSO undergo regiospecific arylation at C‐1 with aryl‐lead triacetates (I) to yield (III) and (VIII), respectively.

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 Hagemann's ester (IIa) and the demethyl analogue (VI) (in equilibrium with the isomer (VII)) in Py/CHCl3 or in DMSO undergo regiospecific arylation at C‐1 with aryl‐lead triacetates (I) to yield (III) and (VIII), respectively.

Key concepts: Chemistry, Yield (engineering), Aryl, Lead (geology), Organic chemistry, Medicinal chemistry, Alkyl, Geomorphology

Related papers

Related paper 1Related paper 2Related paper 3
Back to paper searchBrowse research topicsOriginal source
ChemInform Abstract: Chemistry of Aryl‐Lead(IV) Tricarboxylates. Reaction with Vinylogous β‐Keto Esters. — Research Paper | ScholarLens