Literature DB >> 30093851

Palladium-Catalyzed Triarylation of sp3 C-H Bonds in Heteroarylmethanes: Synthesis of Triaryl(heteroaryl)methanes.

Shuguang Zhang1,2, Bowen Hu2, Zhipeng Zheng2, Patrick J Walsh1,2.   

Abstract

A straightforward method for the palladium-catalyzed triarylation of heteroarylmethanes at the methyl group has been developed. The reaction works with a variety of aryl halides, enabling the rapid synthesis of triaryl(heteroaryl)methanes in moderate to excellent yields.

Entities:  

Keywords:  aryl halides; palladium-catalyzed; tetraarylmethanes; triarylation

Year:  2018        PMID: 30093851      PMCID: PMC6078434          DOI: 10.1002/adsc.201701347

Source DB:  PubMed          Journal:  Adv Synth Catal        ISSN: 1615-4150            Impact factor:   5.837


  29 in total

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Journal:  Chemistry       Date:  2000-10-02       Impact factor: 5.236

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Journal:  Langmuir       Date:  2012-12-19       Impact factor: 3.882

7.  Palladium-catalyzed C(sp3)-H arylation of diarylmethanes at room temperature: synthesis of triarylmethanes via deprotonative-cross-coupling processes.

Authors:  Jiadi Zhang; Ana Bellomo; Andrea D Creamer; Spencer D Dreher; Patrick J Walsh
Journal:  J Am Chem Soc       Date:  2012-08-07       Impact factor: 15.419

8.  Room-temperature palladium-catalyzed direct 2-arylation of benzoxazoles with aryl and heteroaryl bromides.

Authors:  Feng Gao; Byeong-Seon Kim; Patrick J Walsh
Journal:  Chem Commun (Camb)       Date:  2014-07-31       Impact factor: 6.222

9.  Palladium-catalysed synthesis of triaryl(heteroaryl)methanes.

Authors:  Shuguang Zhang; Byeong-Seon Kim; Chen Wu; Jianyou Mao; Patrick J Walsh
Journal:  Nat Commun       Date:  2017-03-14       Impact factor: 14.919

10.  NiXantphos: a deprotonatable ligand for room-temperature palladium-catalyzed cross-couplings of aryl chlorides.

Authors:  Jiadi Zhang; Ana Bellomo; Nisalak Trongsiriwat; Tiezheng Jia; Patrick J Carroll; Spencer D Dreher; Matthew T Tudge; Haolin Yin; Jerome R Robinson; Eric J Schelter; Patrick J Walsh
Journal:  J Am Chem Soc       Date:  2014-04-21       Impact factor: 15.419

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  1 in total

1.  Lewis Basic Salt-Promoted Organosilane Coupling Reactions with Aromatic Electrophiles.

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Journal:  J Am Chem Soc       Date:  2021-07-27       Impact factor: 16.383

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