ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTInfluence of the R group on the brominative formation of 4-bromo-4-R-2,6-di-tert-butylcyclohexadienones from the corresponding phenolsEnrico. Baciocchi and Gabriello. IlluminatiCite this: J. Am. Chem. Soc. 1967, 89, 16, 4017–4019Publication Date (Print):August 1, 1967Publication History Published online1 May 2002Published inissue 1 August 1967https://pubs.acs.org/doi/10.1021/ja00992a012https://doi.org/10.1021/ja00992a012research-articleACS PublicationsRequest reuse permissionsArticle Views128Altmetric-Citations8LEARN 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-Alertsclose Get e-Alerts
Product analyses and kinetic studies of the chlorination in the dark of hexaethylbenzene (I), dodecahydrotriphenylene (II), and trindane (III) in acetic acid solution have shown that all three compounds undergo chlorination by a second-order process which is accompanied by extensive solvolysis. α-Substitution was ascertained in the case of compound (I). This behaviour is wholly analogous to that displayed by hexamethylbenzene. The rate-depression effects are interpreted in terms of ring strain in the transition state for compound (III) and of rigidly interlocked conformations for compound (I). Bromination in the dark is very slow.
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRates and equilibriums for the addition of methoxide ion to 2,6-diphenyl- and 4-methoxy-2,6-diphenylpyrylium cationsGiancarlo Doddi, Simonetta Fornarini, Gabriello Illuminati, and Franco StegelCite this: J. Org. Chem. 1979, 44, 25, 4496–4500Publication Date (Print):December 1, 1979Publication History Published online1 May 2002Published inissue 1 December 1979https://pubs.acs.org/doi/10.1021/jo00393a007https://doi.org/10.1021/jo00393a007research-articleACS PublicationsRequest reuse permissionsArticle Views66Altmetric-Citations11LEARN 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
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTElectronic Transmission through Condensed-ring Systems. II. The Kinetics of Methoxydechlorination of Some 6- and 7-Substituted 1-Aza-4-chloronaphthalenes1,2Gabriello Illuminati and Gianlorenzo MarinoCite this: J. Am. Chem. Soc. 1958, 80, 6, 1421–1424Publication Date (Print):March 1, 1958Publication History Published online1 May 2002Published inissue 1 March 1958https://pubs.acs.org/doi/10.1021/ja01539a035https://doi.org/10.1021/ja01539a035research-articleACS PublicationsRequest reuse permissionsArticle Views60Altmetric-Citations9LEARN 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-Alertsclose Get e-Alerts
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRing closure reactions. III. Synthesis of some medium-sized cyclic aromatic ethers from o-(.omega.-bromoalkyl)phenolsGabriello Illuminati, Luigi Mandolini, and Bernardo MasciCite this: J. Org. Chem. 1974, 39, 17, 2598–2600Publication Date (Print):August 1, 1974Publication History Published online1 May 2002Published inissue 1 August 1974https://pubs.acs.org/doi/10.1021/jo00931a032https://doi.org/10.1021/jo00931a032research-articleACS PublicationsRequest reuse permissionsArticle Views237Altmetric-Citations11LEARN 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-Alertsclose Get e-Alerts
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRing closure reactions of bifunctional chain moleculesGabriello Illuminati and Luigi MandoliniCite this: Acc. Chem. Res. 1981, 14, 4, 95–102Publication Date (Print):April 1, 1981Publication History Published online1 May 2002Published inissue 1 April 1981https://pubs.acs.org/doi/10.1021/ar00064a001https://doi.org/10.1021/ar00064a001research-articleACS PublicationsRequest reuse permissionsArticle Views4745Altmetric-Citations843LEARN 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-Alertsclose Get e-Alerts
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRing-opening reactions. 3. Mechanistic path vs. ring-strain control in elimination and substitution reactions of 1,1-dimethyl cyclic ammonium ions and their .alpha.,.alpha.'-dimethyl-substituted derivativesGabriella Cospito, Gabriello Illuminati, Claudio Lillocci, and Horia PetrideCite this: J. Org. Chem. 1981, 46, 14, 2944–2947Publication Date (Print):July 1, 1981Publication History Published online1 May 2002Published inissue 1 July 1981https://pubs.acs.org/doi/10.1021/jo00327a021https://doi.org/10.1021/jo00327a021research-articleACS PublicationsRequest reuse permissionsArticle Views353Altmetric-Citations32LEARN 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-Alertsclose Get e-Alerts
ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTRing-closure reactions. 7. Kinetics and activation parameters of lactone formation in the range of 3- to 23-membered ringsCarlo Galli, Gabriello Illuminati, Luigi Mandolini, and Pasquale TamborraCite this: J. Am. Chem. Soc. 1977, 99, 8, 2591–2597Publication Date (Print):April 1, 1977Publication History Published online1 May 2002Published inissue 1 April 1977https://pubs.acs.org/doi/10.1021/ja00450a031https://doi.org/10.1021/ja00450a031research-articleACS PublicationsRequest reuse permissionsArticle Views2160Altmetric-Citations116LEARN 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-Alertsclose Get e-Alerts
