Literature DB >> 20386846

A versatile catalyst system for Suzuki-Miyaura syntheses of sterically hindered biaryls employing a cyclobutene-1,2-bis(imidazolium) salt.

Andreas Schmidt1, Alireza Rahimi.   

Abstract

The catalyst system consisting of 3,3'-(3,4-bis(dichloro-methylene)cyclobut-1-ene-1,2-diyl)bis(1-methyl-1H-imidazolium) bis(tetrafluoroborate), Pd(OAc)(2) and NaOtBu in toluene proved to be very effective for a broad variety of Suzuki-Miyaura reactions at room temperature. It is also suited for the synthesis of sterically hindered compounds including 2,6-di-tert-butyl-2'-substituted biaryls at elevated temperatures.

Entities:  

Year:  2010        PMID: 20386846     DOI: 10.1039/c001362e

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  A modified procedure for the palladium catalyzed borylation/Suzuki-Miyaura cross-coupling of aryl and heteroaryl halides utilizing bis-boronic acid.

Authors:  Gary A Molander; Sarah L J Trice; Brittany Tschaen
Journal:  Tetrahedron       Date:  2015-09-02       Impact factor: 2.457

2.  From betaines to anionic N-heterocyclic carbenes. Borane, gold, rhodium, and nickel complexes starting from an imidazoliumphenolate and its carbene tautomer.

Authors:  Ming Liu; Jan C Namyslo; Martin Nieger; Mika Polamo; Andreas Schmidt
Journal:  Beilstein J Org Chem       Date:  2016-12-08       Impact factor: 2.883

  2 in total

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