Chiral Iron Catalysts for Asymmetric Synthesis
This review discusses the development of chiral iron catalysts for asymmetric synthesis, highlighting their advantages such as abundance and low toxicity. It evaluates various ligand designs and catalytic systems, demonstrating significant enantioselectivity improvements and expanding the scope of iron-catalyzed asymmetric reactions.
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTChiral Iron Catalysts for Asymmetric SynthesisKovuru Gopalaiah*View Author Information Department of Chemistry, University of Delhi, Delhi-110007, India*E-mail: [email protected]Cite this: Chem. Rev. 2013, 113, 5, 3248–3296Publication Date (Web):March 5, 2013Publication History Received11 June 2012Published online5 March 2013Published inissue 8 May 2013https://doi.org/10.1021/cr300236rCopyright © 2013 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views14947Altmetric-Citations365LEARN 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 Read OnlinePDF (9 MB) Get e-AlertsSUBJECTS:Catalysts,Hydrocarbons,Iron,Ligands,Stereoselectivity Get e-Alerts
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1
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1
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ADVERTISEMENT RETURN TO ISSUEPREVAddition/CorrectionNEXTORIGINAL ARTICLEThis notice is a correctionCorrection to Polycationic Ligands in Gold Catalysis: Synthesis and Applications of Extremely π-Acidic CatalystsJavier Carreras, Gopinadhanpillai Gopakumar, Lianghu Gu, Ana Gimeno, Pawel Linowski, Jekaterina Petuškova, Walter Thiel, and Manuel Alcarazo*Cite this: J. Am. Chem. Soc. 2014, 136, 8, 3319Publication Date (Web):February 17, 2014Publication History Published online17 February 2014Published inissue 26 February 2014https://doi.org/10.1021/ja413074aCopyright © 2014 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views1601Altmetric-Citations2LEARN 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 (119 KB) Get e-Alerts Get e-Alerts
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23
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ADVERTISEMENT RETURN TO ISSUEPREVCommunication to the...Communication to the EditorNEXTHelical Folding of Poly(naphthalenecarboxamide) Prompted by Solvophobic EffectKoichiro Mikami†, Aya Tanatani‡, Akihiro Yokoyama*†, and Tsutomu Yokozawa*†View Author Information† Department of Material and Life Chemistry, Kanagawa University, Rokkakubashi, Kanagawa-ku, Yokohama 221-8686, Japan‡ Department of Chemistry, Faculty of Science, Ochanomizu University, 2-1-1 Otsuka, Bunkyo-ku, Tokyo 112-8610, Japan*Corresponding authors. E-mail: [email protected], [email protected]Cite this: Macromolecules 2009, 42, 12, 3849–3851Publication Date (Web):May 12, 2009Publication History Received27 March 2009Revised25 April 2009Published online12 May 2009Published inissue 23 June 2009https://pubs.acs.org/doi/10.1021/ma900663qhttps://doi.org/10.1021/ma900663qrapid-communicationACS PublicationsCopyright © 2009 American Chemical SocietyRequest reuse permissionsArticle Views1230Altmetric-Citations22LEARN 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 SUBJECTS:Amides,Aromatic compounds,Circular dichroism spectroscopy,Organic polymers,Solvents Get e-Alerts
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ADVERTISEMENT RETURN TO ISSUEPREVReviewDendrimers Derived from 1 → 3 Branching MotifsGeorge R. Newkome*† and Carol Shreiner‡View Author Information Departments of Polymer Science and Chemistry, University of Akron, Akron, Ohio 44325-4717, and Department of Chemistry, Hiram College, Hiram, Ohio 44234* To whom correspondence should be addressed. E-mail: [email protected]†University of Akron.‡Hiram College.Cite this: Chem. Rev. 2010, 110, 10, 6338–6442Publication Date (Web):July 28, 2010Publication History Received15 October 2009Published online28 July 2010Published inissue 13 October 2010https://pubs.acs.org/doi/10.1021/cr900341mhttps://doi.org/10.1021/cr900341mreview-articleACS PublicationsCopyright © 2010 American Chemical SocietyRequest reuse permissionsArticle Views8279Altmetric-Citations324LEARN 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 SUBJECTS:Amines,Anions,Dendrons,Monomers,Organic compounds Get e-Alerts
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An amphiphilic, water-soluble cyclometalated Pt(II) complex with two-photon emission properties has been developed as a molecular marker specific for in vitro plasma membrane staining.
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ADVERTISEMENT RETURN TO ISSUEPREVCommentNEXTComment on “Observation of the Marcus Inverted Region for Bimolecular Photoinduced Electron-Transfer Reactions in Viscous Media”Gonzalo Angulo*†, Arnulf Rosspeintner‡, Marius Koch§, and Eric Vauthey‡View Author Information† Institute of Physical Chemistry, Polish Academy of Sciences, 44/52 Kasprzaka, 01-224 Warsaw, Poland‡ Department of Physical Chemistry, University of Geneva, 30 Quai Ernest Ansermet, CH-1211 Geneva, Switzerland§ Department of Chemistry, Princeton University, 08540 Princeton, New Jersey, United States*G. Angulo. Fax: +48 22 343 33 33. Tel: +48 22 343 20 86. E-mail: [email protected]Cite this: J. Phys. Chem. B 2016, 120, 36, 9800–9803Publication Date (Web):August 18, 2016Publication History Received1 July 2016Revised24 July 2016Published online30 August 2016Published inissue 15 September 2016https://doi.org/10.1021/acs.jpcb.6b06610Copyright © 2016 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views937Altmetric-Citations5LEARN 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 (495 KB) Get e-AlertsSUBJECTS:Aromatic compounds,Kinetic parameters,Solvents,Transfer reactions,Viscosity Get e-Alerts
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90
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ADVERTISEMENT RETURN TO ISSUEPREVNoteNEXTChemoselective Protection of Carboxylic Acid as Methyl Ester: A Practical Alternative to Diazomethane Protocol†Asit K. Chakraborti, Basak, and Vikas GroverView Author Information Department of Medicinal Chemistry, National Institute of Pharmaceutical Education and Research (NIPER), Sector 67, S. A. S. Nagar 160 062, India, and Department of Chemistry, The University of Burdwan, Burdwan 713 104, India Cite this: J. Org. Chem. 1999, 64, 21, 8014–8017Publication Date (Web):September 23, 1999Publication History Received6 January 1999Published online23 September 1999Published inissue 1 October 1999https://doi.org/10.1021/jo990035lCopyright © 1999 American Chemical SocietyRIGHTS & PERMISSIONSArticle Views6129Altmetric-Citations73LEARN 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 Read OnlinePDF (85 KB) Get e-AlertsSUBJECTS:Alkyls,Chemical reactions,Organic acids,Organic compounds,Organic reactions Get e-Alerts