ADME Study, Molecular Docking, Elucidating the Selectivities and the Mechanism of [4 + 2] Cycloaddition Reaction Between (E)-N ((dimethylamino)methylene)benzothioamide and (S)-3-acryloyl-4-phenyloxazolidin-2-one-Reference-Cited by-同舟云学术

ADME Study, Molecular Docking, Elucidating the Selectivities and the Mechanism of [4 + 2] Cycloaddition Reaction Between (E)-N ((dimethylamino)methylene)benzothioamide and (S)-3-acryloyl-4-phenyloxazolidin-2-one

Published:2024-03-08 Issue: Volume: Page:
ISSN:1073-6085
Container-title:Molecular Biotechnology
language:en
Short-container-title:Mol Biotechnol

Author:

Atif Mhamed,Barhoumi Ali,Syed Asad,Bahkali Ali H.,Chafi Mohammed,Tounsi Abdessamad,Zeroual Abdellah,Paray Bilal Ahamad,Wang Shifa,El Idrissi Mohammed^ORCID

Publisher

Springer Science and Business Media LLC

Link

https://link.springer.com/content/pdf/10.1007/s12033-024-01105-w.pdf

Reference40 articles.

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4. Liu, J., Lu, J., Zhang, C., Zhou, Q., Jamieson, C. S., Shang, C., Houk, K. N., Zhou, J., & Hu, Y. (2023). Tandem intermolecular [4 + 2] cycloadditions are catalysed by glycosylated enzymes for natural product biosynthesis. Nature Chemistry, 15, 1083–1090. https://doi.org/10.1038/s41557-023-01260-8

5. Afzal, U., Bilal, M., Zubair, M., Rasool, N., Shah, S. A. A., & Zakaria, Z. A. (2023). Stereospecific/stereoselective nickel catalyzed reductive cross-coupling: An efficient tool for the synthesis of biological active targeted molecules. Journal of Saudi Chemical Society, 27(1), 101589. https://doi.org/10.1016/j.jscs.2022.101589

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