Analytical-scale synthesis of aryl-SF4Cl via flow microfluidic technology-Reference-Cited by-同舟云学术

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Analytical-scale synthesis of aryl-SF4Cl via flow microfluidic technology

Published:2021-01-07 Issue:2 Volume:11 Page:107-115
ISSN:2062-249X
Container-title:Journal of Flow Chemistry
language:en
Short-container-title:J Flow Chem

Author:

Surjadinata Glen^ORCID,Hunter Luke,Matesic Lidia,Pascali Giancarlo

Funder

Australian Institute of Nuclear Science and Engineering

Department of Education, Employment and Workplace Relations, Australian Government

Publisher

Springer Science and Business Media LLC

Subject

Organic Chemistry,Fluid Flow and Transfer Processes,Chemistry (miscellaneous)

Link

https://link.springer.com/content/pdf/10.1007/s41981-020-00130-5.pdf

Reference21 articles.

1. Altomonte S, Zanda M (2012) Synthetic chemistry and biological activity of pentafluorosulphanyl (SF5) organic molecules. J Fluor Chem 143:57–93. https://doi.org/10.1016/j.jfluchem.2012.06.030

2. Savoie PR, Welch JT (2015) Preparation and utility of organic pentafluorosulfanyl-containing compounds. Chem Rev 115:1130–1190. https://doi.org/10.1021/cr500336u

3. Duveau DY, Hu X, Walsh MJ, Shukla S, Skoumbourdis AP, Boxer MB, Ambudkar SV, Shen M, Thomas CJ (2013) Synthesis and biological evaluation of analogues of the kinase inhibitor nilotinib as Abl and kit inhibitors. Bioorganic Med Chem Lett 23:682–686. https://doi.org/10.1016/j.bmcl.2012.11.111

4. Zhou Y, Wang J, Gu Z, Wang S, Zhu W, Acenã JL, Soloshonok VA, Izawa K, Liu H (2016) Next generation of fluorine-containing pharmaceuticals, compounds currently in phase II-III clinical trials of major pharmaceutical companies: new structural trends and therapeutic areas. Chem Rev 116:422–518. https://doi.org/10.1021/acs.chemrev.5b00392

5. Stump B, Eberle C, Schweizer WB, Kaiser M, Brun R, Krauth-Siegel RL, Lentz D, Diederich F (2009) Pentafluorosulfanyl as a novel building block for enzyme inhibitors: Trypanothione reductase inhibition and antiprotozoal activities of diarylamines. ChemBioChem 10:79–83. https://doi.org/10.1002/cbic.200800565

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3. Oxidative Fluorination of Heteroatoms Enabled by Trichloroisocyanuric Acid and Potassium Fluoride;Angewandte Chemie;2022-06-20

4. Recent Advances in the Synthesis and Medicinal Chemistry of SF5 and SF4Cl Compounds;Synthesis;2022-05-06

5. (Hetero)aryl‐S ^VI Fluorides: Synthetic Development and Opportunities;Angewandte Chemie International Edition;2022-04-27

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