Literature DB >> 29334411

Nickel-Catalyzed C-S Bond Formation via Decarbonylative Thioetherification of Esters, Amides and Intramolecular Recombination Fragment Coupling of Thioesters.

Shao-Chi Lee1, Hsuan-Hung Liao1, Adisak Chatupheeraphat1, Magnus Rueping1,2.   

Abstract

A nickel catalyzed cross-coupling protocol for the straightforward C-S bond formation has been developed. Various mercaptans and a wide range of ester and amide substrates bearing various substituents were tolerated in this process which afforded products in good to excellent yields. Furthermore, an intramolecular protocol for the synthesis of thioethers starting from thioesters has been developed. The utility of this protocol has been demonstrated in a new synthetic protocol of benzothiophene.
© 2018 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  aryl amides; aryl esters; decarbonylation; nickel catalysis; thioesters

Year:  2018        PMID: 29334411     DOI: 10.1002/chem.201705842

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  4 in total

1.  Nickel-Catalyzed Decarbonylative Synthesis of Fluoroalkyl Thioethers.

Authors:  Conor E Brigham; Christian A Malapit; Naish Lalloo; Melanie S Sanford
Journal:  ACS Catal       Date:  2020-07-17       Impact factor: 13.084

2.  Decarbonylative Sulfide Synthesis from Carboxylic Acids and Thioesters via Cross-Over C-S Activation and Acyl Capture.

Authors:  Chengwei Liu; Michal Szostak
Journal:  Org Chem Front       Date:  2021-06-22       Impact factor: 5.456

Review 3.  Thiocoumarins: From the Synthesis to the Biological Applications.

Authors:  Maria J Matos; Lourdes Santana; Eugenio Uriarte; Fernanda Borges
Journal:  Molecules       Date:  2022-07-31       Impact factor: 4.927

4.  Computational Study of Mechanism and Thermodynamics of Ni/IPr-Catalyzed Amidation of Esters.

Authors:  Chong-Lei Ji; Pei-Pei Xie; Xin Hong
Journal:  Molecules       Date:  2018-10-18       Impact factor: 4.411

  4 in total

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