Diversity-oriented synthesis of 1H-1,2,3-triazole tethered pyrazolo[5,1-b]quinazoline hybrids as antimicrobial agents-Reference-Cited by-同舟云学术

Diversity-oriented synthesis of 1H-1,2,3-triazole tethered pyrazolo[5,1-b]quinazoline hybrids as antimicrobial agents

Published:2023-09-11 Issue: Volume: Page:
ISSN:1381-1991
Container-title:Molecular Diversity
language:en
Short-container-title:Mol Divers

Author:

Chudasama Dipakkumar D.,Patel Manan S.,Parekh Jaydeepkumar N.,Patel Harsh C.,Ram Kesur R.

Publisher

Springer Science and Business Media LLC

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Molecular Biology,General Medicine,Information Systems,Catalysis

Link

https://link.springer.com/content/pdf/10.1007/s11030-023-10721-8.pdf

Reference57 articles.

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3. Chen Z, Wu J (2010) Efficient generation of biologically active H-pyrazolo[5,1-a]isoquinolines via multicomponent reaction. Org Lett 12(21):4856–4859. https://doi.org/10.1021/ol101988q

4. Chudasama DD, Patel MS, Parekh JN, Patel HC, Rajput CV, Chikhaliya NP et al (2022) Ultrasound-promoted convenient and ionic liquid [BMIM]BF4 assisted green synthesis of diversely functionalized pyrazolo quinoline core via one-pot multicomponent reaction, DFT study and pharmacological evaluation. Mol Diversity. https://doi.org/10.1007/s11030-022-10498-2

5. Singh H, Sindhu J, Khurana JM, Sharma C, Aneja KR (2014) Ultrasound promoted one pot synthesis of novel fluorescent triazolyl spirocyclic oxindoles using DBU based task specific ionic liquids and their antimicrobial activity. Eur J Med Chem 77:145–154. https://doi.org/10.1016/j.ejmech.2014.03.016

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