Literature DB >> 14961637

Boron trifluoride induced palladium-catalyzed cross-coupling reaction of 1-aryltriazenes with areneboronic acids.

Tomoyuki Saeki1, Eun-Cheol Son, Kohei Tamao.   

Abstract

[reaction: see text] Aryltriazenes are directly coupled with areneboronic acids in the presence of a catalytic amount of Pd(2)(dba)(3) and P(tBu)(3) together with 1 equiv of BF(3).OEt(2) in DME to afford the corresponding biaryl products in up to 98% yield. A carbonylative cross-coupling reaction under a carbon monoxide atmosphere is also found to give the corresponding diaryl ketone with a similar catalyst system.

Entities:  

Year:  2004        PMID: 14961637     DOI: 10.1021/ol036436b

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


  3 in total

1.  Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium complex catalyst.

Authors:  Guangming Nan; Fang Ren; Meiming Luo
Journal:  Beilstein J Org Chem       Date:  2010-06-28       Impact factor: 2.883

2.  Formal group insertion into aryl C‒N bonds through an aromaticity destruction-reconstruction process.

Authors:  Dandan Han; Qiuqin He; Renhua Fan
Journal:  Nat Commun       Date:  2018-08-24       Impact factor: 14.919

3.  Ultrasound-Assisted Hydrazine Reduction Method for the Preparation of Nickel Nanoparticles, Physicochemical Characterization and Catalytic Application in Suzuki-Miyaura Cross-Coupling Reaction.

Authors:  Adél Anna Ádám; Márton Szabados; Gábor Varga; Ádám Papp; Katalin Musza; Zoltán Kónya; Ákos Kukovecz; Pál Sipos; István Pálinkó
Journal:  Nanomaterials (Basel)       Date:  2020-03-28       Impact factor: 5.076

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.