Five-, four-, and three-membered carbocyclic rings from 2-deoxyribose by intramolecular nucleophilic displacement reaction
1991; American Chemical Society; Volume: 56; Issue: 21 Linguagem: Inglês
10.1021/jo00021a015
ISSN1520-6904
Autores Tópico(s)Cyclopropane Reaction Mechanisms
ResumoADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTFive-, four-, and three-membered carbocyclic rings from 2-deoxyribose by intramolecular nucleophilic displacement reactionKarsten Krohn and Guido BoernerCite this: J. Org. Chem. 1991, 56, 21, 6038–6043Publication Date (Print):October 1, 1991Publication History Published online1 May 2002Published inissue 1 October 1991https://doi.org/10.1021/jo00021a015RIGHTS & PERMISSIONSArticle Views521Altmetric-Citations19LEARN 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 InReddit PDF (839 KB) Get e-Alerts Get e-Alerts
Referência(s)