Vinyl alcohol. Generation and decay kinetics in aqueous solution and determination of the tautomerization equilibrium constant and acid dissociation constants of the aldehyde and enol forms

Citations Over TimeTop 1% of 1987 papers

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTVinyl alcohol. Generation and decay kinetics in aqueous solution and determination of the tautomerization equilibrium constant and acid dissociation constants of the aldehyde and enol formsY. Chiang, M. Hojatti, J. R. Keeffe, A. J. Kresge, N. P. Schepp, and J. WirzCite this: J. Am. Chem. Soc. 1987, 109, 13, 4000–4009Publication Date (Print):June 1, 1987Publication History Published online1 May 2002Published inissue 1 June 1987https://pubs.acs.org/doi/10.1021/ja00247a028https://doi.org/10.1021/ja00247a028research-articleACS PublicationsRequest reuse permissionsArticle Views723Altmetric-Citations106LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-AlertscloseSupporting Info (1)»Supporting Information Supporting Information Get e-Alerts

Related Papers

• → Identification, classification and relative stability of tautomers in the cambridge structural database(2010)68 cited
• → Tautobase: An Open Tautomer Database(2020)41 cited
• → Direct demonstration of tautomeric nature of 4‐bromo‐3(5)‐methylpyrazoles(2022)4 cited
• → The tautomerism of 6-hydroxy-, 6-amino- and 6-acylamino-7-azaindolines(1966)19 cited
• → Studies on the Tautomerism of 2-Anilinopyridine and Related Heterocycles. II. 2-Anilino-5-nitropyridine and 2-Anilinopyrimidine(1980)9 cited