Literature DB >> 16956213

Selective substituent transfer from mixed zinc reagents in Ni-catalyzed anhydride alkylation.

Jeffrey B Johnson1, Robert T Yu, Paul Fink, Eric A Bercot, Tomislav Rovis.   

Abstract

The use of mixed zinc reagents in Ni-catalyzed anhydride alkylation results in preferential transfer of substituents (Ph > Me > Et >> iPr approximately TMSCH2) for the ligands bipy, dppe, and iPrPHOX. Utilization of such mixed species allows the use of 0.55 equiv of the diorganozinc reagent, effectively transferring both desired substituents when used in conjunction with a suitable second zinc reagent.

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Year:  2006        PMID: 16956213     DOI: 10.1021/ol0616337

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  5 in total

1.  Activation of C-O and C-N Bonds Using Non-Precious-Metal Catalysis.

Authors:  Timothy B Boit; Ana S Bulger; Jacob E Dander; Neil K Garg
Journal:  ACS Catal       Date:  2020-09-10       Impact factor: 13.084

2.  Breaking Amides using Nickel Catalysis.

Authors:  Jacob E Dander; Neil K Garg
Journal:  ACS Catal       Date:  2017-01-06       Impact factor: 13.084

3.  Nickel-Catalyzed Alkylation of Amide Derivatives.

Authors:  Bryan J Simmons; Nicholas A Weires; Jacob E Dander; Neil K Garg
Journal:  ACS Catal       Date:  2016-04-12       Impact factor: 13.084

4.  Using JPP to Identify Ni Bidentate Phosphine Complexes In Situ.

Authors:  Matthew D Hannigan; Anne J McNeil; Paul M Zimmerman
Journal:  Inorg Chem       Date:  2021-08-18       Impact factor: 5.165

5.  Ni-Catalyzed Suzuki-Miyaura Cross-Coupling of Aliphatic Amides on the Benchtop.

Authors:  Milauni M Mehta; Timothy B Boit; Jacob E Dander; Neil K Garg
Journal:  Org Lett       Date:  2019-10-17       Impact factor: 6.005

  5 in total

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