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An efficient continuous-flow synthesis and evaluation of antimicrobial activity of novel 1,2,3-Triazole-Furan hybrid chalcone derivatives
An efficient continuous-flow synthetic protocol developed for novel 1,2,3-triazole-furan hybrid chalcone derivatives by Claisen-Schmidt condensation of 1-phenyl-1H-1,2,3-triazole-4-carbaldehydes with 2-acetylfuran using KOH as base catalyst. The newly synthesized chalcones characterized by using dif...
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Published in: | Chemical Data Collections 2020-08, Vol.28, p.100457, Article 100457 |
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Main Authors: | , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | An efficient continuous-flow synthetic protocol developed for novel 1,2,3-triazole-furan hybrid chalcone derivatives by Claisen-Schmidt condensation of 1-phenyl-1H-1,2,3-triazole-4-carbaldehydes with 2-acetylfuran using KOH as base catalyst. The newly synthesized chalcones characterized by using different spectral data such as IR, 1HNMR, 13CNMR, mass spectrometry and elemental analysis. The antimicrobial screening of the chalcone derivatives results showed that the compounds 3 h and 3i have most promising activity.
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ISSN: | 2405-8300 2405-8300 |
DOI: | 10.1016/j.cdc.2020.100457 |