Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2022 Apr;26(2):1249-1258.
doi: 10.1007/s11030-021-10227-1. Epub 2021 May 12.

Supported Cu(II)-Schiff base: novel heterogeneous catalyst with extremely high activity for eco-friendly, one-pot and multi-component C-S bond-forming reaction toward a wide range of thioethers as biologically active cores

Affiliations

Supported Cu(II)-Schiff base: novel heterogeneous catalyst with extremely high activity for eco-friendly, one-pot and multi-component C-S bond-forming reaction toward a wide range of thioethers as biologically active cores

Pezhman Shiri et al. Mol Divers. 2022 Apr.

Abstract

An effective and proficient process for the synthesis of a variety of thioethers via the one-step reaction of benzyl halides, aryl halides, and thiourea is presented. This strategy is a one-pot procedure to achieve a variety of thioethers without the requirement to thiols as starting compounds. A range of thioethers containing electron donating/electron-withdrawing functional groups were obtained with good to excellent yields under mild conditions. Moreover, the nanocatalyst exhibited excellent recyclability for the reaction, making it more sustainable. One-pot and multi-component synthesis, high yields of final products, green reaction media, high activity of nanocatalyst, simple separation of the products and catalyst, and high regioselectivity are several highlights of this method.

Keywords: Cu(II)-complex; C–S Bond-forming reaction; Green media; Odorless intermediates; One pot; Thioether.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Weber L (2002) Multi-component reactions and evolutionary chemistry. Drug Discov Today 7:143–147. https://doi.org/10.1016/s1359-6446(02)00010-7 - DOI - PubMed
    1. Zolfigol MA, Khazaei A, Moosavi-Zare AR, Zare A, Asgari Z, Khakyzadeh V, Hasaninejad A (2013) Design of ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate as a dual-catalyst for the one-pot multi-component synthesis of 1,2,4,5-tetrasubstituted imidazoles. J Ind Eng Chem 19:721–726. https://doi.org/10.1016/j.jiec.2012.10.014 - DOI
    1. Daraei M, Zolfigol MA, Derakhshan-Panah F, Shiri M, Kruger HG, Mokhlesi M (2015) Synthesis of tetrahydropyridines by one-pot multicomponent reaction using nano-sphere silica sulfuric acid. J Iran Chem Soc 12:855–861. https://doi.org/10.1007/s13738-014-0548-x - DOI
    1. Hall DG, Rybak T, Verdelet T (2016) Multicomponent hetero-[4 + 2] cycloaddition/allylboration reaction: from natural product synthesis to drug discovery. Acc Chem Res 49:2489–2500. https://doi.org/10.1021/acs.accounts.6b00403 - DOI - PubMed
    1. Ruijter E, Orru RVA (2013) Multicomponent reactions-opportunities for the pharmaceutical industry. Drug Discov Today Technol 10:e15–e20. https://doi.org/10.1016/j.ddtec.2012.10.012 - DOI - PubMed

LinkOut - more resources