Literature DB >> 11506627

Sterically demanding, water-soluble alkylphosphines as ligands for high activity Suzuki coupling of aryl bromides in aqueous solvents.

K H Shaughnessy1, R S Booth.   

Abstract

[reaction: see text]. Sterically demanding, water-soluble alkylphosphines have been found to give highly active catalysts for Suzuki coupling of aryl bromides in aqueous solvents. A variety of aryl bromides and boronic acids were coupled in excellent yield. Turnover numbers up to 734 000 mmol/mmol Pd have been achieved under mild conditions.

Entities:  

Year:  2001        PMID: 11506627     DOI: 10.1021/ol0163629

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


  4 in total

1.  Studies on Pd/NiFe(2)O(4) catalyzed ligand-free Suzuki reaction in aqueous phase: synthesis of biaryls, terphenyls and polyaryls.

Authors:  Sanjay R Borhade; Suresh Babsaheb Waghmode
Journal:  Beilstein J Org Chem       Date:  2011-03-15       Impact factor: 2.883

Review 2.  Prospects and Applications of Palladium Nanoparticles in the Cross-coupling of (hetero)aryl Halides and Related Analogues.

Authors:  Jude I Ayogu; Efeturi A Onoabedje
Journal:  ChemistryOpen       Date:  2021-02-15       Impact factor: 2.630

3.  A general synthesis of C8-arylpurine phosphoramidites.

Authors:  Vorasit Vongsutilers; Jonathan R Daft; Kevin H Shaughnessy; Peter M Gannett
Journal:  Molecules       Date:  2009-09-02       Impact factor: 4.411

4.  The synthesis of some perhydrobenzimidazolinium salts and their application in pd-carbene catalyzed heck and suzuki reactions.

Authors:  Murat Yiğit
Journal:  Molecules       Date:  2009-06-05       Impact factor: 4.411

  4 in total

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