Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements

The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkyla...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Canadian journal of chemistry 2011-11, Vol.89 (10), p.1236-1244
Hauptverfasser: Rajesh, Kancherla, Reddy, Bandapalli Palakshi, Vijayakumar, Vijayaparthasarathi
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1244
container_issue 10
container_start_page 1236
container_title Canadian journal of chemistry
container_volume 89
creator Rajesh, Kancherla
Reddy, Bandapalli Palakshi
Vijayakumar, Vijayaparthasarathi
description The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).
doi_str_mv 10.1139/v11-088
format Article
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_gale_infotraccpiq_272167759</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A272167759</galeid><sourcerecordid>A272167759</sourcerecordid><originalsourceid>FETCH-LOGICAL-c546t-6581747c925dfd83a38f443c4126de6bba5b34ba3d4c4acef0170195f98f37a73</originalsourceid><addsrcrecordid>eNqV0t1qFDEUB_BBFFyr-ApDBUVpar5mJnNZitZCreDHdcgkJ7spu5lpklmdOx_CJ-yTGLstdWErSC6SE375B5JTFM8JPiSEtW_XhCAsxINiRrjAiNGWPCxmGGOBOOb0cfEkxotcNphWs2I679ewLDs39EYtD8oUblfKmzJBCuq6LskBR8YtJhP6YQrOOA-xvPr5q_zodOi_qzUgFaOLCUwZJ58WkIvrkJjCqNMYcojuvc0HV-BTfFo8smoZ4dnNvFd8e__u6_EHdPbp5PT46AzpitcJ1ZUgDW90SytjjWCKCcs505zQ2kDddarqGO8UM1xzpcFi0mDSVrYVljWqYXvF_iZ3CP3lCDHJi34MPl8pRZuTq5bijF7chyinTHCOm_pOzdUSpPO2z8-jVy5qeUQbSuomp2WFdqg5eMhP0HuwLm9v-f0dXg_uUv6NDnegPAysnN6Z-nrrQDYJfqS5GmOUp18-_4c937avNjb_eowBrByCW6kwSYLlnwaUuQFlbsAs32ykDzpABBX04h_45f34BsnBWPYb-xzl4A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2423844076</pqid></control><display><type>article</type><title>Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements</title><source>Free Full-Text Journals in Chemistry</source><creator>Rajesh, Kancherla ; Reddy, Bandapalli Palakshi ; Vijayakumar, Vijayaparthasarathi</creator><creatorcontrib>Rajesh, Kancherla ; Reddy, Bandapalli Palakshi ; Vijayakumar, Vijayaparthasarathi</creatorcontrib><description>The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).</description><identifier>ISSN: 0008-4042</identifier><identifier>EISSN: 1480-3291</identifier><identifier>DOI: 10.1139/v11-088</identifier><identifier>CODEN: CJCHAG</identifier><language>eng</language><publisher>Ottawa: NRC Research Press</publisher><subject>1,4-dihydropyridines bipodes ; Alkylation ; Ammonia ; Ammonium ; Ammonium acetate ; Benzaldehyde ; bipodal-tripodal-tetrapodal 1,4-dihydropyridines ; Chemical compounds ; Chemical reactions ; Chemical synthesis ; Hantzsch pyridines ; Hydroxybenzaldehydes ; irradiation microonde ; microwave irradiation ; NMR ; Nuclear magnetic resonance ; Pyridine ; pyridines de Hantzsch ; Structure ; tripodes ou tétrapodes</subject><ispartof>Canadian journal of chemistry, 2011-11, Vol.89 (10), p.1236-1244</ispartof><rights>COPYRIGHT 2011 NRC Research Press</rights><rights>2011 Published by NRC Research Press</rights><rights>Copyright National Research Council of Canada Oct 2011</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c546t-6581747c925dfd83a38f443c4126de6bba5b34ba3d4c4acef0170195f98f37a73</citedby><cites>FETCH-LOGICAL-c546t-6581747c925dfd83a38f443c4126de6bba5b34ba3d4c4acef0170195f98f37a73</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>Rajesh, Kancherla</creatorcontrib><creatorcontrib>Reddy, Bandapalli Palakshi</creatorcontrib><creatorcontrib>Vijayakumar, Vijayaparthasarathi</creatorcontrib><title>Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements</title><title>Canadian journal of chemistry</title><description>The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).</description><subject>1,4-dihydropyridines bipodes</subject><subject>Alkylation</subject><subject>Ammonia</subject><subject>Ammonium</subject><subject>Ammonium acetate</subject><subject>Benzaldehyde</subject><subject>bipodal-tripodal-tetrapodal 1,4-dihydropyridines</subject><subject>Chemical compounds</subject><subject>Chemical reactions</subject><subject>Chemical synthesis</subject><subject>Hantzsch pyridines</subject><subject>Hydroxybenzaldehydes</subject><subject>irradiation microonde</subject><subject>microwave irradiation</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pyridine</subject><subject>pyridines de Hantzsch</subject><subject>Structure</subject><subject>tripodes ou tétrapodes</subject><issn>0008-4042</issn><issn>1480-3291</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNqV0t1qFDEUB_BBFFyr-ApDBUVpar5mJnNZitZCreDHdcgkJ7spu5lpklmdOx_CJ-yTGLstdWErSC6SE375B5JTFM8JPiSEtW_XhCAsxINiRrjAiNGWPCxmGGOBOOb0cfEkxotcNphWs2I679ewLDs39EYtD8oUblfKmzJBCuq6LskBR8YtJhP6YQrOOA-xvPr5q_zodOi_qzUgFaOLCUwZJ58WkIvrkJjCqNMYcojuvc0HV-BTfFo8smoZ4dnNvFd8e__u6_EHdPbp5PT46AzpitcJ1ZUgDW90SytjjWCKCcs505zQ2kDddarqGO8UM1xzpcFi0mDSVrYVljWqYXvF_iZ3CP3lCDHJi34MPl8pRZuTq5bijF7chyinTHCOm_pOzdUSpPO2z8-jVy5qeUQbSuomp2WFdqg5eMhP0HuwLm9v-f0dXg_uUv6NDnegPAysnN6Z-nrrQDYJfqS5GmOUp18-_4c937avNjb_eowBrByCW6kwSYLlnwaUuQFlbsAs32ykDzpABBX04h_45f34BsnBWPYb-xzl4A</recordid><startdate>20111101</startdate><enddate>20111101</enddate><creator>Rajesh, Kancherla</creator><creator>Reddy, Bandapalli Palakshi</creator><creator>Vijayakumar, Vijayaparthasarathi</creator><general>NRC Research Press</general><general>Canadian Science Publishing NRC Research Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>ISN</scope><scope>ISR</scope></search><sort><creationdate>20111101</creationdate><title>Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements</title><author>Rajesh, Kancherla ; Reddy, Bandapalli Palakshi ; Vijayakumar, Vijayaparthasarathi</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c546t-6581747c925dfd83a38f443c4126de6bba5b34ba3d4c4acef0170195f98f37a73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>1,4-dihydropyridines bipodes</topic><topic>Alkylation</topic><topic>Ammonia</topic><topic>Ammonium</topic><topic>Ammonium acetate</topic><topic>Benzaldehyde</topic><topic>bipodal-tripodal-tetrapodal 1,4-dihydropyridines</topic><topic>Chemical compounds</topic><topic>Chemical reactions</topic><topic>Chemical synthesis</topic><topic>Hantzsch pyridines</topic><topic>Hydroxybenzaldehydes</topic><topic>irradiation microonde</topic><topic>microwave irradiation</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pyridine</topic><topic>pyridines de Hantzsch</topic><topic>Structure</topic><topic>tripodes ou tétrapodes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Rajesh, Kancherla</creatorcontrib><creatorcontrib>Reddy, Bandapalli Palakshi</creatorcontrib><creatorcontrib>Vijayakumar, Vijayaparthasarathi</creatorcontrib><collection>CrossRef</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><jtitle>Canadian journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Rajesh, Kancherla</au><au>Reddy, Bandapalli Palakshi</au><au>Vijayakumar, Vijayaparthasarathi</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements</atitle><jtitle>Canadian journal of chemistry</jtitle><date>2011-11-01</date><risdate>2011</risdate><volume>89</volume><issue>10</issue><spage>1236</spage><epage>1244</epage><pages>1236-1244</pages><issn>0008-4042</issn><eissn>1480-3291</eissn><coden>CJCHAG</coden><abstract>The one pot, three component reaction of p-hydroxy benzaldehyde, β-ketoester, and ammonium acetate afforded the corresponding monopodal 1,4-dihydropyridines as building blocks, which in turn converted into diversified novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines with different alkylating agents through conventional as well as microwave assisted reactions. The unambiguous structural confinements of the all the synthesized compounds were drawn out with the help of 2D NMR (H-H COSY and C-H COSY).</abstract><cop>Ottawa</cop><pub>NRC Research Press</pub><doi>10.1139/v11-088</doi><tpages>9</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0008-4042
ispartof Canadian journal of chemistry, 2011-11, Vol.89 (10), p.1236-1244
issn 0008-4042
1480-3291
language eng
recordid cdi_gale_infotraccpiq_272167759
source Free Full-Text Journals in Chemistry
subjects 1,4-dihydropyridines bipodes
Alkylation
Ammonia
Ammonium
Ammonium acetate
Benzaldehyde
bipodal-tripodal-tetrapodal 1,4-dihydropyridines
Chemical compounds
Chemical reactions
Chemical synthesis
Hantzsch pyridines
Hydroxybenzaldehydes
irradiation microonde
microwave irradiation
NMR
Nuclear magnetic resonance
Pyridine
pyridines de Hantzsch
Structure
tripodes ou tétrapodes
title Novel bipodal, tripodal, and tetrapodal 1,4-dihydropyridines — Microwave-assisted synthesis and structural confinements
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T19%3A33%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Novel%20bipodal,%20tripodal,%20and%20tetrapodal%201,4-dihydropyridines%20%E2%80%94%20Microwave-assisted%20synthesis%20and%20structural%20confinements&rft.jtitle=Canadian%20journal%20of%20chemistry&rft.au=Rajesh,%20Kancherla&rft.date=2011-11-01&rft.volume=89&rft.issue=10&rft.spage=1236&rft.epage=1244&rft.pages=1236-1244&rft.issn=0008-4042&rft.eissn=1480-3291&rft.coden=CJCHAG&rft_id=info:doi/10.1139/v11-088&rft_dat=%3Cgale_proqu%3EA272167759%3C/gale_proqu%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2423844076&rft_id=info:pmid/&rft_galeid=A272167759&rfr_iscdi=true