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Synthesis and anti-microbial activity of new (1-alkyl-1h-1,2,3-triazol-4-yl)methyl-2hchromene-3-carboxylates : a click chemistry approach
A series of new 1,4 disubstituted (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3- carboxylates (4ai–4eiii) have been efficiently synthesized in moderate to excellent yields by the 1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a–e and various alkyl azides under Cu(I) c...
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Published in: | Journal of Saudi Chemical Society 2015, Vol.19 (4), p.372-378 |
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container_end_page | 378 |
container_issue | 4 |
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container_title | Journal of Saudi Chemical Society |
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creator | Reddy, M. Koteswara Rao, Y. Jayaprakash Krupadanam, G. L. David |
description | A series of new 1,4 disubstituted (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-
carboxylates (4ai–4eiii) have been efficiently synthesized in moderate to excellent yields by the
1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a–e and various alkyl
azides under Cu(I) catalyzed conditions. The structures of the synthesized compounds are established
based on IR, NMR, MASS Spectrometric methods and elemental analyses. The antibacterial
and antifungal activities of synthesized compounds were evaluated. Compounds 4biii, 4ei, 4dii, 4ai,
4aii, 4bii showed good activity against bacterial strains and the compounds 4bi, 4eii against fungal
strains. |
format | article |
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carboxylates (4ai–4eiii) have been efficiently synthesized in moderate to excellent yields by the
1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a–e and various alkyl
azides under Cu(I) catalyzed conditions. The structures of the synthesized compounds are established
based on IR, NMR, MASS Spectrometric methods and elemental analyses. The antibacterial
and antifungal activities of synthesized compounds were evaluated. Compounds 4biii, 4ei, 4dii, 4ai,
4aii, 4bii showed good activity against bacterial strains and the compounds 4bi, 4eii against fungal
strains.</description><identifier>ISSN: 1319-6103</identifier><language>eng</language><publisher>Riyadh, Saudi Arabia: Saudi Chemical Society</publisher><subject>Carboxylates ; Chemical-biological activities ; Synthesis ; Triazoles</subject><ispartof>Journal of Saudi Chemical Society, 2015, Vol.19 (4), p.372-378</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids></links><search><creatorcontrib>Reddy, M. Koteswara</creatorcontrib><creatorcontrib>Rao, Y. Jayaprakash</creatorcontrib><creatorcontrib>Krupadanam, G. L. David</creatorcontrib><title>Synthesis and anti-microbial activity of new (1-alkyl-1h-1,2,3-triazol-4-yl)methyl-2hchromene-3-carboxylates : a click chemistry approach</title><title>Journal of Saudi Chemical Society</title><description>A series of new 1,4 disubstituted (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-
carboxylates (4ai–4eiii) have been efficiently synthesized in moderate to excellent yields by the
1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a–e and various alkyl
azides under Cu(I) catalyzed conditions. The structures of the synthesized compounds are established
based on IR, NMR, MASS Spectrometric methods and elemental analyses. The antibacterial
and antifungal activities of synthesized compounds were evaluated. Compounds 4biii, 4ei, 4dii, 4ai,
4aii, 4bii showed good activity against bacterial strains and the compounds 4bi, 4eii against fungal
strains.</description><subject>Carboxylates</subject><subject>Chemical-biological activities</subject><subject>Synthesis</subject><subject>Triazoles</subject><issn>1319-6103</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><recordid>eNqFic1KQzEQRrNQsGgfQZilQgeSm9q_rSjudV-m6VwyNrm5JKEa38C39gruPfBxPjgXamas2eLKaHul5qW861_WutObmfp-bUP1XKQADcdpVTCKy-kgFIBclbPUBqmHgT_gziCFUwtoPJpFt7BYs9BXCrjEFu4jVz_FzjufU-SB0aKjfEifLVDlAjsgcEHcCZznKKXmBjSOOZHzN-qyp1B4_udrdfv89Pb4ghwpc0_7Mcv02v5hq-1maf_rPydKTk4</recordid><startdate>2015</startdate><enddate>2015</enddate><creator>Reddy, M. Koteswara</creator><creator>Rao, Y. Jayaprakash</creator><creator>Krupadanam, G. L. David</creator><general>Saudi Chemical Society</general><scope>ADJCN</scope><scope>AHFXO</scope></search><sort><creationdate>2015</creationdate><title>Synthesis and anti-microbial activity of new (1-alkyl-1h-1,2,3-triazol-4-yl)methyl-2hchromene-3-carboxylates : a click chemistry approach</title><author>Reddy, M. Koteswara ; Rao, Y. Jayaprakash ; Krupadanam, G. L. David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-emarefa_primary_5903843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Carboxylates</topic><topic>Chemical-biological activities</topic><topic>Synthesis</topic><topic>Triazoles</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reddy, M. Koteswara</creatorcontrib><creatorcontrib>Rao, Y. Jayaprakash</creatorcontrib><creatorcontrib>Krupadanam, G. L. David</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><jtitle>Journal of Saudi Chemical Society</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reddy, M. Koteswara</au><au>Rao, Y. Jayaprakash</au><au>Krupadanam, G. L. David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and anti-microbial activity of new (1-alkyl-1h-1,2,3-triazol-4-yl)methyl-2hchromene-3-carboxylates : a click chemistry approach</atitle><jtitle>Journal of Saudi Chemical Society</jtitle><date>2015</date><risdate>2015</risdate><volume>19</volume><issue>4</issue><spage>372</spage><epage>378</epage><pages>372-378</pages><issn>1319-6103</issn><abstract>A series of new 1,4 disubstituted (1-alkyl-1H-1,2,3-triazol-4-yl)methyl-2H-chromene-3-
carboxylates (4ai–4eiii) have been efficiently synthesized in moderate to excellent yields by the
1,3 dipolar cycloaddition between 2-propynyl-2H-chromene-3-carboxylates 3a–e and various alkyl
azides under Cu(I) catalyzed conditions. The structures of the synthesized compounds are established
based on IR, NMR, MASS Spectrometric methods and elemental analyses. The antibacterial
and antifungal activities of synthesized compounds were evaluated. Compounds 4biii, 4ei, 4dii, 4ai,
4aii, 4bii showed good activity against bacterial strains and the compounds 4bi, 4eii against fungal
strains.</abstract><cop>Riyadh, Saudi Arabia</cop><pub>Saudi Chemical Society</pub><tpages>7</tpages></addata></record> |
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source | ScienceDirect (Online service); IngentaConnect Journals |
subjects | Carboxylates Chemical-biological activities Synthesis Triazoles |
title | Synthesis and anti-microbial activity of new (1-alkyl-1h-1,2,3-triazol-4-yl)methyl-2hchromene-3-carboxylates : a click chemistry approach |
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