Literature DB >> 30397992

Carbonylative C-C Bond Activation of Electron-Poor Cyclopropanes: Rhodium-Catalyzed (3+1+2) Cycloadditions of Cyclopropylamides.

Andrew G Dalling1, Takayuki Yamauchi1, Niall G McCreanor1, Lydia Cox1, John F Bower1.   

Abstract

Rh-catalyzed carbonylative C-C bond activation of cyclopropylamides generates configurationally stable rhodacyclopentanones that engage tethered alkenes in (3+1+2) cycloadditions. These studies provide the first examples of multicomponent cycloadditions that proceed through C-C bond activation of "simple" electron poor cyclopropanes.
© 2019 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  C−C activation; cycloaddition; cyclopropane; rhodium

Year:  2018        PMID: 30397992     DOI: 10.1002/anie.201811460

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

1.  Carbonylative N-Heterocyclization via Nitrogen-Directed C-C Bond Activation of Nonactivated Cyclopropanes.

Authors:  Adam D J Calow; David Dailler; John F Bower
Journal:  J Am Chem Soc       Date:  2022-06-17       Impact factor: 16.383

2.  An endo-Directing-Group Strategy Unlocks Enantioselective (3+1+2) Carbonylative Cycloadditions of Aminocyclopropanes.

Authors:  Olga O Sokolova; John F Bower
Journal:  Angew Chem Int Ed Engl       Date:  2022-06-24       Impact factor: 16.823

  2 in total

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