1970•Journal of Mass SpectrometryRequires access

Mass spectrometry of tautomeric compounds—II: A mechanism of ketene elimination from enol acetates

Hisao Nakata, Akira Tatematsu

Open publisher page 8 citations

Abstract

Comparisons of the mass spectral behaviour of the [M – 42] ions from enol acetates and that of the corresponding ketones indicate that the elimination of a ketene molecule from enol acetates proceeded through a four-membered cyclic transition state to afford fragment ions with an enolic structure.

About this research paper

What this paper is about

Comparisons of the mass spectral behaviour of the [M – 42] ions from enol acetates and that of the corresponding ketones indicate that the elimination of a ketene molecule from enol acetates proceeded through a four-membered cyclic transition state to afford fragment ions with an enolic structure.

Why it matters

OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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

Comparisons of the mass spectral behaviour of the [M – 42] ions from enol acetates and that of the corresponding ketones indicate that the elimination of a ketene molecule from enol acetates proceeded through a four-membered cyclic transition state to afford fragment ions with an enolic structure.

Key concepts: Ketene, Enol, Tautomer, Chemistry, Mass spectrometry, Keto–enol tautomerism, Molecule, Computational chemistry

Related papers

Back to paper searchBrowse research topicsOriginal source
Mass spectrometry of tautomeric compounds—II: A mechanism of ketene elimination from enol acetates — Research Paper | ScholarLens