Optimization of the synthesis of het/aryl-amidoximes using an efficient green chemistry-Reference-Cited by-同舟云学术

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Optimization of the synthesis of het/aryl-amidoximes using an efficient green chemistry

Published:2020-03-11 Issue:8 Volume:50 Page:1217-1231
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Albayati Mustafa R.¹,Mohamed Mamdouh F. A.²,Moustafa Amr H.³^ORCID

Affiliation:

1. Department of Chemistry, College of Education, Kirkuk University, Kirkuk, Iraq;

2. Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Sohag University, Sohag, Egypt;

3. Department of Chemistry, Faculty of Science, Sohag University, Sohag, Egypt

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2020.1735443

Reference60 articles.

1. Amidoximes and Oximes: Synthesis, Structure, and Their Key Role as NO Donors

2. The Chemistry of Amidoximes and Related Compounds.

3. A novel synthesis of 1,2,4-oxadiazoles and isoxazoles

4. Novel aryl carboximidamide and 3-aryl-1,2,4-oxadiazole analogues of naproxen as dual selective COX-2/15-LOX inhibitors: Design, synthesis and docking studies

5. The first one-pot ambient-temperature synthesis of 1,2,4-oxadiazoles from amidoximes and carboxylic acid esters

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1. Design, synthesis and preliminary antibacterial evaluation of novel 1,3-benzoxazole/carboximidamide- and 1,3-benzoxazole/3-aryl-1,2,4-oxadiazole hybrids;Journal of Molecular Structure;2024-08

2. Regiospecific synthesis of N,N’ -disubstituted-2-imino-hydantoins derived from cyanamides;Synthetic Communications;2024-06-18

3. Design, synthesis, molecular docking, ADMET studies, and biological activity evaluation of new 2-({[3-aryl-1,2,4-oxadiazol-5-yl)methyl]thio}-1H-benzimidazoles and 6-amino-6-aryl-5,6-dihydro[1,6,2,4]oxathiadiazocino[4,5-a]benzimidazol-3(2H)-ones;Journal of Molecular Structure;2024-01

4. An efficient synthesis of new 3,5‐bis(2‐arylthiazol‐4‐yl)‐1,2,4‐oxadiazole derivatives and their antimicrobial evaluation;Journal of Heterocyclic Chemistry;2023-03-11

5. Eco-friendly and regiospecific intramolecular cyclization reactions of cyano and carbonyl groups in N,N-disubstituted cyanamide;Molecular Diversity;2022-02-27

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