Literature DB >> 20704186

Transition-metal-free Sonogashira-type coupling of ortho-substituted aryl and alkynyl Grignard reagents by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical as an oxidant.

Modhu Sudan Maji1, Sandip Murarka, Armido Studer.   

Abstract

Cross coupling of aryl, alkenyl, and alkynyl magnesium compounds by using 2,2,6,6-tetramethylpiperidine-N-oxyl radical (TEMPO) as an environmentally benign organic oxidant is described. This coupling reaction can be performed without adding any transition metal on various ortho-substituted aryl and alkynyl Grignard reagents. Importantly, functional groups such as esters, amides, and cyanides are shown to be tolerated under the reaction conditions.

Entities:  

Year:  2010        PMID: 20704186     DOI: 10.1021/ol1015702

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


  4 in total

1.  Aminoxyl-Catalyzed Electrochemical Diazidation of Alkenes Mediated by a Metastable Charge-Transfer Complex.

Authors:  Juno C Siu; Joseph B Parry; Song Lin
Journal:  J Am Chem Soc       Date:  2019-01-28       Impact factor: 15.419

2.  Transition-metal-free alkynylation of aryl chlorides.

Authors:  Thanh Truong; Olafs Daugulis
Journal:  Org Lett       Date:  2011-07-25       Impact factor: 6.005

3.  Copper-catalyzed oxidative homo- and cross-coupling of Grignard reagents using diaziridinone.

Authors:  Yingguang Zhu; Tao Xiong; Wenyong Han; Yian Shi
Journal:  Org Lett       Date:  2014-11-24       Impact factor: 6.005

4.  Chromium-catalyzed para-selective formation of quaternary carbon centers by alkylation of benzamide derivatives.

Authors:  Pei Liu; Changpeng Chen; Xuefeng Cong; Jinghua Tang; Xiaoming Zeng
Journal:  Nat Commun       Date:  2018-11-06       Impact factor: 14.919

  4 in total

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