Literature DB >> 30675616

Controlled Ni-catalyzed mono- and double-decarbonylations of α-ketothioesters.

Zhao-Jing Zheng1, Cheng Jiang, Peng-Cheng Shao, Wen-Fei Liu, Tian-Tian Zhao, Peng-Fei Xu, Hao Wei.   

Abstract

A method for Ni-catalyzed controlled decarbonylation of α-ketothioesters is described. Mono- and double-decarbonylations, which gave thioesters and thioethers, respectively, were selectively achieved by changing the ligand. A fundamental study of Ni-catalyzed decarbonylation of α-ketothioesters is presented.

Entities:  

Year:  2019        PMID： 30675616     DOI： 10.1039/c8cc09352k

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN： 1359-7345            Impact factor:   6.222


  3 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.  Forging C-S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides.

Authors:  Chengwei Liu; Michal Szostak
Journal:  ChemCatChem       Date:  2021-09-25       Impact factor: 5.497

3.  Cobalt-catalyzed intramolecular decarbonylative coupling of acylindoles and diarylketones through the cleavage of C-C bonds.

Authors:  Tian-Yang Yu; Wen-Hua Xu; Hong Lu; Hao Wei
Journal:  Chem Sci       Date:  2020-10-16       Impact factor: 9.825
  3 in total

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