Literature DB >> 12733884

Room-temperature Hiyama cross-couplings of arylsilanes with alkyl bromides and iodides.

Jae-Young Lee1, Gregory C Fu.   

Abstract

The first method for achieving Hiyama couplings of unactivated alkyl bromides and iodides is reported. The desired carbon-carbon bond formation proceeds under mild conditions (room temperature) with good functional-group tolerance.

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Year:  2003        PMID： 12733884     DOI： 10.1021/ja0349352

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN： 0002-7863            Impact factor:   15.419


  4 in total

1.  Ligand-enabled cross-coupling of C(sp(3))-H bonds with arylsilanes.

Authors:  Jian He; Ryosuke Takise; Haiyan Fu; Jin-Quan Yu
Journal:  J Am Chem Soc       Date:  2015-04-02       Impact factor: 15.419

2.  Transition-Metal (Pd, Ni, Mn)-Catalyzed C-C Bond Constructions Involving Unactivated Alkyl Halides and Fundamental Synthetic Building Blocks.

Authors:  Megan R Kwiatkowski; Erik J Alexanian
Journal:  Acc Chem Res       Date:  2019-03-25       Impact factor: 22.384

3.  Gold-catalyzed oxidative coupling reactions with aryltrimethylsilanes.

Authors:  William E Brenzovich; Jean-François Brazeau; F Dean Toste
Journal:  Org Lett       Date:  2010-11-05       Impact factor: 6.005

Review 4.  Transition Metal Catalyzed Hiyama Cross-Coupling: Recent Methodology Developments and Synthetic Applications.

Authors:  Rida Noor; Ameer Fawad Zahoor; Muhammad Irfan; Syed Makhdoom Hussain; Sajjad Ahmad; Ali Irfan; Katarzyna Kotwica-Mojzych; Mariusz Mojzych
Journal:  Molecules       Date:  2022-09-02       Impact factor: 4.927
  4 in total

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