Forging C−S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides-Reference-Cited by-同舟云学术

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

Published:2021-10-12 Issue:23 Volume:13 Page:4878-4881
ISSN:1867-3880
Container-title:ChemCatChem
language:en
Short-container-title:ChemCatChem

Author:

Liu Chengwei¹^ORCID,Szostak Michal²^ORCID

Affiliation:

1. School of Chemistry and Materials Science Nanjing University of Information Science and Technology 219 Ningliu Road Nanjing Jiangsu 210044 China

2. Department of Chemistry Rutgers University 73 Warren Street Newark NJ 07102 USA

Funder

National Institutes of Health

National Science Foundation

Nanjing University of Information Science and Technology

Publisher

Wiley

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Catalysis

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/cctc.202101206

Reference64 articles.

1.

2. Modern Arylation Methods

3. Modern Nucleophilic Aromatic Substitution

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1. Heterogeneously catalyzed decarbonylation of thioesters by supported Ni, Pd, or Rh nanoparticle catalysts;Organic & Biomolecular Chemistry;2024

2. Decarbonylative borylation of aryl anhydrides via rhodium catalysis;Organic & Biomolecular Chemistry;2024

3. Nickel-catalyzed synthesis of aryl sulfides from aromatic primary amides and thioethers via aryl exchange strategy;Journal of Organometallic Chemistry;2023-12

4. Access to thioethers from thiols and alcohols via homogeneous and heterogeneous catalysis;Scientific Reports;2023-11-23

5. Nickel-Catalyzed Decarbonylation of α-Oxyacetic Acid Thioesters: Hydroxymethylation of Mercaptans;Synlett;2023-08-23

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