Literature DB >> 30483696

An enantioselective synthesis of α-alkylated pyrroles via cooperative isothiourea/palladium catalysis.

W Rush Scaggs1, Toya D Scaggs, Thomas N Snaddon.   

Abstract

Herein we describe the direct enantioselective Lewis base/Pd catalysed α-allylation of pyrrole acetic acid esters. This provides high isolated yields of highly enantioenriched products and exhibits broad reaction scope with respect to both reaction partners. The products can be readily elaborated in a manner which points towards potential applications in target directed synthesis.

Entities:  

Year:  2019        PMID: 30483696      PMCID: PMC6499370          DOI: 10.1039/c8ob02600a

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  3 in total

Review 1.  Recent progress in asymmetric synergistic catalysis - the judicious combination of selected chiral aminocatalysts with achiral metal catalysts.

Authors:  Christian D-T Nielsen; Joshua D Linfoot; Alexander F Williams; Alan C Spivey
Journal:  Org Biomol Chem       Date:  2022-04-06       Impact factor: 3.890

2.  Cooperative Palladium/Isothiourea Catalyzed Enantioselective Formal (3+2) Cycloaddition of Vinylcyclopropanes and α,β-Unsaturated Esters.

Authors:  Jacqueline Bitai; Alastair J Nimmo; Alexandra M Z Slawin; Andrew D Smith
Journal:  Angew Chem Int Ed Engl       Date:  2022-04-28       Impact factor: 16.823

3.  Isothiourea-Catalyzed Enantioselective Michael Addition of Malonates to α,β-Unsaturated Aryl Esters.

Authors:  Jiufeng Wu; Claire M Young; Amy A Watts; Alexandra M Z Slawin; Gregory R Boyce; Michael Bühl; Andrew D Smith
Journal:  Org Lett       Date:  2022-06-02       Impact factor: 6.072

  3 in total

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