Literature DB >> 19173659

Nickel-catalyzed [4 + 2] cycloaddition of enones with alkynes.

Ichiro Koyama1, Takuya Kurahashi, Seijiro Matsubara.   

Abstract

A nickel-catalyzed [4 + 2] cycloaddition reaction has been developed where enones react with alkynes to afford polysubstituted pyrans. A mechanistic rationale is proposed, implying oxa-nickela cycle formation by oxidative cyclization of nickel to enone, followed by alkyne insertion.

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Year:  2009        PMID: 19173659     DOI: 10.1021/ja807952r

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  2 in total

1.  Predictable and regioselective insertion of internal unsymmetrical alkynes in rhodium-catalyzed cycloadditions with alkenyl isocyanates.

Authors:  Rebecca Keller Friedman; Tomislav Rovis
Journal:  J Am Chem Soc       Date:  2009-08-05       Impact factor: 15.419

2.  Ligand-field transition-induced C-S bond formation from nickelacycles.

Authors:  Jeongcheol Shin; Jiseon Lee; Jong-Min Suh; Kiyoung Park
Journal:  Chem Sci       Date:  2021-11-10       Impact factor: 9.825

  2 in total

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