Loading…
Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents
Pd‐mediated construction of pyridine scaffold and subsequent Suzuki‐based C—C coupling reaction in one pot has been accomplished for the synthesis of 4‐biaryl substituted 2‐amino‐3‐cyanopyridines via multicomponent reaction. The present multicomponent reaction is useful in structural elaboration of...
Saved in:
Published in: | Journal of heterocyclic chemistry 2014-08, Vol.51 (S1), p.E104-E113 |
---|---|
Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3 |
---|---|
cites | cdi_FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3 |
container_end_page | E113 |
container_issue | S1 |
container_start_page | E104 |
container_title | Journal of heterocyclic chemistry |
container_volume | 51 |
creator | Srinivasula Reddy, L. Ram Reddy, T. Gangi Reddy, N. C. Mohan, Reddy Bodireddy Lingappa, Y. |
description | Pd‐mediated construction of pyridine scaffold and subsequent Suzuki‐based C—C coupling reaction in one pot has been accomplished for the synthesis of 4‐biaryl substituted 2‐amino‐3‐cyanopyridines via multicomponent reaction. The present multicomponent reaction is useful in structural elaboration of pyridine framework and also helpful in design and synthesis of novel and diverse analogs of complex heterocyclic compounds other than present reported molecules. Antibacterial activities of the synthesized compounds were systematically evaluated. The correlation between functional group variation and biological activities of the compounds has been evaluated against human pathogenic gram‐positive and gram‐negative bacterial strains. |
doi_str_mv | 10.1002/jhet.1855 |
format | article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1566841724</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1566841724</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3</originalsourceid><addsrcrecordid>eNp1kc9uEzEQxlcIJELhwBtY4gKHbdf2ev9wK6u0adXSiKQQcbHc3dnEqWOnthe6fb4-GN4k4oDExaMZ_75Pmvmi6D1OjnGSkJP1CvwxLhh7EY1wmdKY4ZK-jEbhj8SYkcXr6I1z69Bimuej6HnaxNfQSOGhQded8rI2m63RoD2a9dqvwEmHTIsmcrlSPTrrdO2l0ULJp6CY9lY2UoNDQjeoMtrBQxe0UihUxVWYdFsl9RLduuGddU_dvUTfQOxMkNToRgOaGv8ZzVcgLbrQ6Lv01qDxL6E6saOEG4iD62kod0EOdtctw9i9jV61Qjl4d6hH0e3ZeF5N4qub84vq9CquKaMsJnla1LTEKSRY0IbWSd2wFlom6qzIWUbaMitImjYkY-KuBVJCuBrL0iQvS0KBHkUf975ba8KazvONdDUoJTSYznHMsqxIcU7SgH74B12bzoazDRTLc5ZkjAbq056qrXHOQsu3Vm6E7TlO-JAnH_LkQ56BPdmzv6WC_v8gv5yM5wdFvFdI5-Hxr0LYe57lNGf8x9dz_rOcLb4weskX9A8w6rPj</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1557750653</pqid></control><display><type>article</type><title>Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents</title><source>Wiley</source><creator>Srinivasula Reddy, L. ; Ram Reddy, T. ; Gangi Reddy, N. C. ; Mohan, Reddy Bodireddy ; Lingappa, Y.</creator><creatorcontrib>Srinivasula Reddy, L. ; Ram Reddy, T. ; Gangi Reddy, N. C. ; Mohan, Reddy Bodireddy ; Lingappa, Y.</creatorcontrib><description>Pd‐mediated construction of pyridine scaffold and subsequent Suzuki‐based C—C coupling reaction in one pot has been accomplished for the synthesis of 4‐biaryl substituted 2‐amino‐3‐cyanopyridines via multicomponent reaction. The present multicomponent reaction is useful in structural elaboration of pyridine framework and also helpful in design and synthesis of novel and diverse analogs of complex heterocyclic compounds other than present reported molecules. Antibacterial activities of the synthesized compounds were systematically evaluated. The correlation between functional group variation and biological activities of the compounds has been evaluated against human pathogenic gram‐positive and gram‐negative bacterial strains.</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.1855</identifier><language>eng</language><publisher>Hoboken: Blackwell Publishing Ltd</publisher><ispartof>Journal of heterocyclic chemistry, 2014-08, Vol.51 (S1), p.E104-E113</ispartof><rights>2014 HeteroCorporation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3</citedby><cites>FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Srinivasula Reddy, L.</creatorcontrib><creatorcontrib>Ram Reddy, T.</creatorcontrib><creatorcontrib>Gangi Reddy, N. C.</creatorcontrib><creatorcontrib>Mohan, Reddy Bodireddy</creatorcontrib><creatorcontrib>Lingappa, Y.</creatorcontrib><title>Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents</title><title>Journal of heterocyclic chemistry</title><addtitle>J. Heterocyclic Chem</addtitle><description>Pd‐mediated construction of pyridine scaffold and subsequent Suzuki‐based C—C coupling reaction in one pot has been accomplished for the synthesis of 4‐biaryl substituted 2‐amino‐3‐cyanopyridines via multicomponent reaction. The present multicomponent reaction is useful in structural elaboration of pyridine framework and also helpful in design and synthesis of novel and diverse analogs of complex heterocyclic compounds other than present reported molecules. Antibacterial activities of the synthesized compounds were systematically evaluated. The correlation between functional group variation and biological activities of the compounds has been evaluated against human pathogenic gram‐positive and gram‐negative bacterial strains.</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNp1kc9uEzEQxlcIJELhwBtY4gKHbdf2ev9wK6u0adXSiKQQcbHc3dnEqWOnthe6fb4-GN4k4oDExaMZ_75Pmvmi6D1OjnGSkJP1CvwxLhh7EY1wmdKY4ZK-jEbhj8SYkcXr6I1z69Bimuej6HnaxNfQSOGhQded8rI2m63RoD2a9dqvwEmHTIsmcrlSPTrrdO2l0ULJp6CY9lY2UoNDQjeoMtrBQxe0UihUxVWYdFsl9RLduuGddU_dvUTfQOxMkNToRgOaGv8ZzVcgLbrQ6Lv01qDxL6E6saOEG4iD62kod0EOdtctw9i9jV61Qjl4d6hH0e3ZeF5N4qub84vq9CquKaMsJnla1LTEKSRY0IbWSd2wFlom6qzIWUbaMitImjYkY-KuBVJCuBrL0iQvS0KBHkUf975ba8KazvONdDUoJTSYznHMsqxIcU7SgH74B12bzoazDRTLc5ZkjAbq056qrXHOQsu3Vm6E7TlO-JAnH_LkQ56BPdmzv6WC_v8gv5yM5wdFvFdI5-Hxr0LYe57lNGf8x9dz_rOcLb4weskX9A8w6rPj</recordid><startdate>201408</startdate><enddate>201408</enddate><creator>Srinivasula Reddy, L.</creator><creator>Ram Reddy, T.</creator><creator>Gangi Reddy, N. C.</creator><creator>Mohan, Reddy Bodireddy</creator><creator>Lingappa, Y.</creator><general>Blackwell Publishing Ltd</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>201408</creationdate><title>Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents</title><author>Srinivasula Reddy, L. ; Ram Reddy, T. ; Gangi Reddy, N. C. ; Mohan, Reddy Bodireddy ; Lingappa, Y.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Srinivasula Reddy, L.</creatorcontrib><creatorcontrib>Ram Reddy, T.</creatorcontrib><creatorcontrib>Gangi Reddy, N. C.</creatorcontrib><creatorcontrib>Mohan, Reddy Bodireddy</creatorcontrib><creatorcontrib>Lingappa, Y.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Srinivasula Reddy, L.</au><au>Ram Reddy, T.</au><au>Gangi Reddy, N. C.</au><au>Mohan, Reddy Bodireddy</au><au>Lingappa, Y.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><addtitle>J. Heterocyclic Chem</addtitle><date>2014-08</date><risdate>2014</risdate><volume>51</volume><issue>S1</issue><spage>E104</spage><epage>E113</epage><pages>E104-E113</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>Pd‐mediated construction of pyridine scaffold and subsequent Suzuki‐based C—C coupling reaction in one pot has been accomplished for the synthesis of 4‐biaryl substituted 2‐amino‐3‐cyanopyridines via multicomponent reaction. The present multicomponent reaction is useful in structural elaboration of pyridine framework and also helpful in design and synthesis of novel and diverse analogs of complex heterocyclic compounds other than present reported molecules. Antibacterial activities of the synthesized compounds were systematically evaluated. The correlation between functional group variation and biological activities of the compounds has been evaluated against human pathogenic gram‐positive and gram‐negative bacterial strains.</abstract><cop>Hoboken</cop><pub>Blackwell Publishing Ltd</pub><doi>10.1002/jhet.1855</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0022-152X |
ispartof | Journal of heterocyclic chemistry, 2014-08, Vol.51 (S1), p.E104-E113 |
issn | 0022-152X 1943-5193 |
language | eng |
recordid | cdi_proquest_miscellaneous_1566841724 |
source | Wiley |
title | Pd-Mediated Multicomponent Synthesis of Highly Functionalized Pyridines and Consequential C-C Coupling Using Suzuki Reaction in One Pot: Their In Vitro Evaluation as Potential Antibacterial Agents |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T11%3A44%3A06IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Pd-Mediated%20Multicomponent%20Synthesis%20of%20Highly%20Functionalized%20Pyridines%20and%20Consequential%20C-C%20Coupling%20Using%20Suzuki%20Reaction%20in%20One%20Pot:%20Their%20In%20Vitro%20Evaluation%20as%20Potential%20Antibacterial%20Agents&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Srinivasula%20Reddy,%20L.&rft.date=2014-08&rft.volume=51&rft.issue=S1&rft.spage=E104&rft.epage=E113&rft.pages=E104-E113&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.1855&rft_dat=%3Cproquest_cross%3E1566841724%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c3535-2748c3914e01a3d3c0cd5fef5ac687562f968244d265abfe29e022564079923e3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=1557750653&rft_id=info:pmid/&rfr_iscdi=true |