Quantifying the Reactivity of a Remarkably Long-Lived Difluorinated Enol in Acidic Methanol via Solution Kinetics and Electronic Structure Calculations-Reference-Cited by-同舟云学术

Quantifying the Reactivity of a Remarkably Long-Lived Difluorinated Enol in Acidic Methanol via Solution Kinetics and Electronic Structure Calculations

Published:2006-09-22 Issue:21 Volume:71 Page:8250-8255
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Griffith Gerry A.¹,Hillier Ian H.¹,Percy Jonathan M.¹,Roig Ricard¹,Vincent Mark A.¹

Affiliation:

1. Department of Chemistry, University of Leicester, University Road, Leicester LE1 7RH, United Kingdom, School of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, United Kingdom, and Pure and Applied Chemistry, WestCHEM, University of Strathclyde, Thomas Graham Building, 295 Cathedral Street, Glasgow G1 1XL, United Kingdom

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061450y

Reference42 articles.

1. Generation of simple enols in solution

2. Ingold Lecture. Reactive intermediates: carboxylic acid enols and other unstable species

3. Recent advances in the chemistry of stable simple enols

4. Simple enols. 1. The generation of vinyl alcohol in solution and its detection and characterization by NMR spectroscopy

5. Simple enols. 2. Kinetics and mechanism of the ketonization of vinyl alcohol

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