Demonstration of controlled asymmetric induction in organoiron chemistry. Suggestions concerning the specification of chirality in pseudotetrahedral metal complexes containing polyhapto ligands

Citations Over TimeTop 10% of 1975 papers

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTDemonstration of controlled asymmetric induction in organoiron chemistry. Suggestions concerning the specification of chirality in pseudotetrahedral metal complexes containing polyhapto ligandsK. Stanley and M. C. BairdCite this: J. Am. Chem. Soc. 1975, 97, 22, 6598–6599Publication Date (Print):October 1, 1975Publication History Published online1 May 2002Published inissue 1 October 1975https://pubs.acs.org/doi/10.1021/ja00855a063https://doi.org/10.1021/ja00855a063research-articleACS PublicationsRequest reuse permissionsArticle Views321Altmetric-Citations155LEARN 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

Related Papers

• → Enantioselective creation of helical chirality in octahedral (OC-6) complexes. Recent advances(1998)57 cited
• → Absolute Stereochemical Determination of Asymmetric Sulfoxides via Central to Axial Induction of Chirality(2017)22 cited
• → Helical Chirality Induction in Zinc Bilindiones by Amino Acid Esters and Amines(1998)53 cited
• → 1,3-Asymmetric induction: Highly enantioselective synthesis of α-amino acids via 2,5-trans disubstituted imidazolidin-4-ones(1991)12 cited
• → Memory of Chirality: Asymmetric Induction Based on the Dynamic Chirality of Enolates.(2003)3 cited