PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 8, 2003Chemical Reviews1,478 citations

The Asymmetric Intramolecular Heck Reaction in Natural Product Total Synthesis

View Full Paper
ADAmy B. DounayLOLarry E. Overman

Key Points

Key points are not available for this paper at this time.

Abstract

ADVERTISEMENT RETURN TO ISSUEPREVArticleNEXTThe Asymmetric Intramolecular Heck Reaction in Natural Product Total SynthesisAmy B. Dounay and Larry E. OvermanView Author Information Department of Chemistry, University of California, Irvine, California 92697-2025 Cite this: Chem. Rev. 2003, 103, 8, 2945–2964Publication Date (Web):July 8, 2003Publication History Received5 February 2003Published online8 July 2003Published inissue 1 August 2003https://pubs.acs.org/doi/10.1021/cr020039hhttps://doi.org/10.1021/cr020039hresearch-articleACS PublicationsCopyright © 2003 American Chemical SocietyRequest reuse permissionsArticle Views24937Altmetric-Citations1345LEARN 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:Cyclization,Heck reaction,Hydrocarbons,Ligands,Stereoselectivity Get e-Alerts

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Dounay et al. (2003) studied this question.

synapsesocial.com/papers/6a20bb561d1b409c7a11d257https://doi.org/10.1021/cr020039h
Ask AI
Helpful
Bookmark
Share
View Full Paper

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Asymmetric Heck Reactions via Neutral Intermediates: Enhanced Enantioselectivity with Halide Additives Gives Mechanistic Insights1997 · 112 citations
  2. 2Correction. Catalytic Asymmetric Synthesis of Benzylic Quaternary Carbon Centers. An Efficient Synthesis of (-)-Eptazocine1994 · 65 citations
  3. 3Total synthesis of (+)-halenaquinol and (+)-halenaquinone. Experimental proof of their absolute stereostructures theoretically determined1988 · 67 citations
  4. 4Total Synthesis of (−)-Spirotryprostatin B and Three Stereoisomers2000 · 131 citations
  5. 5Enantioselective Total Synthesis of Quadrigemine C and Psycholeine2002 · 167 citations