Synthesis, characterization and in vitro bioactivity studies of isoindolin‐1‐3‐phosophonate compounds-Reference-Cited by-同舟云学术

Synthesis, characterization and in vitro bioactivity studies of isoindolin‐1‐3‐phosophonate compounds

Published:2022-01-17 Issue: Volume: Page:
ISSN:0022-152X
Container-title:Journal of Heterocyclic Chemistry
language:en
Short-container-title:Journal of Heterocyclic Chem

Author:

Jelali Hamida¹,Al Nasr Ibrahim S.²³,Koko Waleed S.³,Khan Tariq A.⁴,Deniau Eric⁵,Sauthier Mathieu⁵,Alresheedi Faisal⁶,Hamdi Naceur¹⁷

Affiliation:

1. Research Laboratory of Environmental Sciences and Technologies (LR16ES09), Higher Institute of Environmental Sciences and Technology University of Carthage Hammam‐Lif Tunisia

2. Department of Biology, College of Science and Arts Qassim University Unaizah Saudi Arabia

3. Department of Science Laboratories, College of Science and Arts Qassim University Ar Rass Saudi Arabia

4. Department of Biomedical Instrumentation, College of Applied Health Sciences Qassim University Ar Rass Saudi Arabia

5. Université de Lille, UMR CNRS 8181, Unité de Catalyse et Chimie du Solide, USTL–ENSCL Villeneuve d'Ascq cedex France

6. Department of Physics, College of Science Qassim University Buraidah Saudi Arabia

7. Department of Chemistry, College of Science and Arts Qassim University Ar Rass Saudi Arabia

Publisher

Wiley

Subject

Organic Chemistry

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jhet.4396

Reference70 articles.

1. Isoindole Derivatives: Propitious Anticancer Structural Motifs

2. Efficient PhB(OH)2-catalyzed one-pot synthesis of 3-substituted isoindolin-1-ones and isobenzofuran-1(3H)-ones under solvent free conditions

3. Practical synthesis of 3-(2-arylethylidene)isoindolin-1-ones (analogues of AKS-182) and 3-(2-arylethylidene)isobenzofuran-1(3H)-ones

4. Co(II)-Catalyzed Desilylative Annulation of Benzamides and Acrylamides with Alkynylsilanes: Access to 3-Methyleneisoindolin-1-one and 5-Methylene-1H-pyrrol-2(5H)-one Derivatives

5. A facile, protic ionic liquid route to N-substituted 5-hydroxy-4-methyl-3-oxoisoindoline-1-carboxamides and N-substituted 3-oxoisoindoline-4-carboxylic acids

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