Literature DB >> 23461805

TMPZnOPiv•LiCl: a new base for the preparation of air-stable solid zinc pivalates of sensitive aromatics and heteroaromatics.

Christos I Stathakis1, Sophia M Manolikakes, Paul Knochel.   

Abstract

A wide range of aryl and heteroaryl zinc pivalates bearing sensitive functionalities were prepared by selective metalation using TMPZnOPiv•LiCl, a new hindered zinc amide base. The new zinc reagents are easy-to-handle solids, which maintain their activity almost entirely (>95%) after 4 h of air exposure and smoothly undergo Negishi cross-couplings and reactions with various electrophiles such as Cu(I)-catalyzed acylations and allylations.

Entities:  

Year:  2013        PMID: 23461805     DOI: 10.1021/ol400242r

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


  4 in total

1.  Synthesis of solid 2-pyridylzinc reagents and their application in Negishi reactions.

Authors:  James R Colombe; Sebastian Bernhardt; Christos Stathakis; Stephen L Buchwald; Paul Knochel
Journal:  Org Lett       Date:  2013-10-24       Impact factor: 6.005

Review 2.  Synthetic and medicinal perspective of quinolines as antiviral agents.

Authors:  Ramandeep Kaur; Kapil Kumar
Journal:  Eur J Med Chem       Date:  2021-01-24       Impact factor: 6.514

3.  Organozinc pivalates for cobalt-catalyzed difluoroalkylarylation of alkenes.

Authors:  Xinyi Cheng; Xingchen Liu; Shengchun Wang; Ying Hu; Binjing Hu; Aiwen Lei; Jie Li
Journal:  Nat Commun       Date:  2021-07-16       Impact factor: 14.919

4.  Mechanochemical Activation of Zinc and Application to Negishi Cross-Coupling.

Authors:  Qun Cao; Joseph L Howard; Emilie Wheatley; Duncan L Browne
Journal:  Angew Chem Int Ed Engl       Date:  2018-08-02       Impact factor: 15.336

  4 in total

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