An effective green one-pot synthesis of some novel 5-(thiophene-2-carbonyl)-6-(trifluoromethyl)pyrano[2,3-c]pyrazoles and 6-(thiophene-2-carbonyl)-7-(trifluoromethyl)pyrano[2,3-d]pyrimidines bearing chromone ring as anticancer agents-Reference-Cited by-同舟云学术

An effective green one-pot synthesis of some novel 5-(thiophene-2-carbonyl)-6-(trifluoromethyl)pyrano[2,3-c]pyrazoles and 6-(thiophene-2-carbonyl)-7-(trifluoromethyl)pyrano[2,3-d]pyrimidines bearing chromone ring as anticancer agents

Published:2021-09-20 Issue:21 Volume:51 Page:3267-3276
ISSN:0039-7911
Container-title:Synthetic Communications
language:en
Short-container-title:Synthetic Communications

Author:

Ali Tarik E.¹²,Assiri Mohammed A.¹,Alzahrani Abdullah Y.³,Salem Mohamed A.³⁴,Shati Ali A.⁵,Alfaifi Mohammad Y.⁵,Elbehairi Serag Eldin I.⁵⁶

Affiliation:

1. Faculty of Science, Department of Chemistry, King Khalid University, Abha, Saudi Arabia

2. Faculty of Education, Department of Chemistry, Ain Shams University, Cairo, Egypt

3. Faculty of Science and Arts, Department of Chemistry, King Khalid University, Mohail Assir, Saudi Arabia

4. Faculty of Science, Department of Chemistry, Al-Azhar University, Nasr City, Egypt

5. Faculty of Science, Department of Biology, King Khalid University, Abha, Saudi Arabia

6. Cell Culture Lab, Egyptian Organization for Biological Products and Vaccines (VACSERA Holding Company), Agouza, Egypt

Funder

King Khalid University

Publisher

Informa UK Limited

Subject

Organic Chemistry

Link

https://www.tandfonline.com/doi/pdf/10.1080/00397911.2021.1966804

Reference28 articles.

1. Ligand-based CoMFA and CoMSIA studies on chromone derivatives as radical scavengers

2. Synthesis and Anticonvulsant Activity of Certain Substituted Furochromone, Benzofuran and Flavone Derivatives

3. Design, synthesis, antimicrobial and antioxidant activity of 3-formyl chromone hydrazone and their metal (II) complexes

4. The synthesis and anticancer activities of chiral epoxy-substituted chromone analogs

5. 2H-Pyran-2-ones and their annelated analogs as multifaceted building blocks for the fabrication of diverse heterocycles

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