Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides

α‐Imino carbonyl compounds − derivatives of 3‐imidazoline nitroxides − were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5‐triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthe...

Full description

Saved in:
Bibliographic Details
Published in:European journal of organic chemistry 2003-11, Vol.2003 (22), p.4432-4437
Main Authors: Roshchupkina, Galina A., Pervukhina, Natalie V., Rybalova, Tatjana V., Gatilov, Yuri V., Burdukov, Alexey B., Reznikov, Vladimir A.
Format: Article
Language:English
Subjects:
Heterocycles
Ketones
Luminescence
Nitroxides
Radiochemistry
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by
cites
container_end_page 4437
container_issue 22
container_start_page 4432
container_title European journal of organic chemistry
container_volume 2003
creator Roshchupkina, Galina A.
Pervukhina, Natalie V.
Rybalova, Tatjana V.
Gatilov, Yuri V.
Burdukov, Alexey B.
Reznikov, Vladimir A.
description α‐Imino carbonyl compounds − derivatives of 3‐imidazoline nitroxides − were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5‐triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthesized were verified by X‐ray analysis of the mixed‐ligand complexes with copper hexafluoroacetylacetonate. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)
doi_str_mv 10.1002/ejoc.200300212
format article
fullrecord <record><control><sourceid>istex_wiley</sourceid><recordid>TN_cdi_wiley_primary_10_1002_ejoc_200300212_EJOC200300212</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_HZK9SBBW_0</sourcerecordid><originalsourceid>FETCH-LOGICAL-i2412-3c6680cc03e916bec8d0eac04ea47f56cb8aa1a247169150142315761c9c030a3</originalsourceid><addsrcrecordid>eNo9kN9OwjAUhxejiYjeer0HsHjabh29lIEMJZD4JxhvmtKVWBwr6SYynsBr38QX8SF8EocYrs7vl5zv5OTzvHMMLQxALvXcqhYBoHXB5MBrYOAcAeNwWOeABghz-nTsnRTFHAA4Y7jhLRNdamdVpTKzkaWxuX-npfoLduZ_f6HBwuTWj6Wb2rzK_NgulvYtTwv_5-PT72pnVjW20sV2nVyEqGteqtRZhBNkFiaVG5tpf2RKZ9cm1cWpdzSTWaHP_mfTe7zuPcQJGo77g_hqiAwJMEFUMdYGpYBqjtlUq3YK9V8QaBlEs5CpaVtKLEkQYcZxCDggFIcRw4rXDEja9Pju7rvJdCWWziykqwQGsZUltrLEXpbo3YzjfatZtGNNUer1npXuVbCIRqGYjPoieb7l953ORAD9BXqbcbI</addsrcrecordid><sourcetype>Publisher</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides</title><source>Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)</source><creator>Roshchupkina, Galina A. ; Pervukhina, Natalie V. ; Rybalova, Tatjana V. ; Gatilov, Yuri V. ; Burdukov, Alexey B. ; Reznikov, Vladimir A.</creator><creatorcontrib>Roshchupkina, Galina A. ; Pervukhina, Natalie V. ; Rybalova, Tatjana V. ; Gatilov, Yuri V. ; Burdukov, Alexey B. ; Reznikov, Vladimir A.</creatorcontrib><description>α‐Imino carbonyl compounds − derivatives of 3‐imidazoline nitroxides − were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5‐triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthesized were verified by X‐ray analysis of the mixed‐ligand complexes with copper hexafluoroacetylacetonate. (© Wiley‐VCH Verlag GmbH &amp; Co. KGaA, 69451 Weinheim, Germany, 2003)</description><identifier>ISSN: 1434-193X</identifier><identifier>EISSN: 1099-0690</identifier><identifier>DOI: 10.1002/ejoc.200300212</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Heterocycles ; Ketones ; Luminescence ; Nitroxides ; Radiochemistry</subject><ispartof>European journal of organic chemistry, 2003-11, Vol.2003 (22), p.4432-4437</ispartof><rights>Copyright © 2003 WILEY‐VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Roshchupkina, Galina A.</creatorcontrib><creatorcontrib>Pervukhina, Natalie V.</creatorcontrib><creatorcontrib>Rybalova, Tatjana V.</creatorcontrib><creatorcontrib>Gatilov, Yuri V.</creatorcontrib><creatorcontrib>Burdukov, Alexey B.</creatorcontrib><creatorcontrib>Reznikov, Vladimir A.</creatorcontrib><title>Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides</title><title>European journal of organic chemistry</title><addtitle>Eur. J. Org. Chem</addtitle><description>α‐Imino carbonyl compounds − derivatives of 3‐imidazoline nitroxides − were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5‐triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthesized were verified by X‐ray analysis of the mixed‐ligand complexes with copper hexafluoroacetylacetonate. (© Wiley‐VCH Verlag GmbH &amp; Co. KGaA, 69451 Weinheim, Germany, 2003)</description><subject>Heterocycles</subject><subject>Ketones</subject><subject>Luminescence</subject><subject>Nitroxides</subject><subject>Radiochemistry</subject><issn>1434-193X</issn><issn>1099-0690</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><recordid>eNo9kN9OwjAUhxejiYjeer0HsHjabh29lIEMJZD4JxhvmtKVWBwr6SYynsBr38QX8SF8EocYrs7vl5zv5OTzvHMMLQxALvXcqhYBoHXB5MBrYOAcAeNwWOeABghz-nTsnRTFHAA4Y7jhLRNdamdVpTKzkaWxuX-npfoLduZ_f6HBwuTWj6Wb2rzK_NgulvYtTwv_5-PT72pnVjW20sV2nVyEqGteqtRZhBNkFiaVG5tpf2RKZ9cm1cWpdzSTWaHP_mfTe7zuPcQJGo77g_hqiAwJMEFUMdYGpYBqjtlUq3YK9V8QaBlEs5CpaVtKLEkQYcZxCDggFIcRw4rXDEja9Pju7rvJdCWWziykqwQGsZUltrLEXpbo3YzjfatZtGNNUer1npXuVbCIRqGYjPoieb7l953ORAD9BXqbcbI</recordid><startdate>20031114</startdate><enddate>20031114</enddate><creator>Roshchupkina, Galina A.</creator><creator>Pervukhina, Natalie V.</creator><creator>Rybalova, Tatjana V.</creator><creator>Gatilov, Yuri V.</creator><creator>Burdukov, Alexey B.</creator><creator>Reznikov, Vladimir A.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope></search><sort><creationdate>20031114</creationdate><title>Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides</title><author>Roshchupkina, Galina A. ; Pervukhina, Natalie V. ; Rybalova, Tatjana V. ; Gatilov, Yuri V. ; Burdukov, Alexey B. ; Reznikov, Vladimir A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-i2412-3c6680cc03e916bec8d0eac04ea47f56cb8aa1a247169150142315761c9c030a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Heterocycles</topic><topic>Ketones</topic><topic>Luminescence</topic><topic>Nitroxides</topic><topic>Radiochemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Roshchupkina, Galina A.</creatorcontrib><creatorcontrib>Pervukhina, Natalie V.</creatorcontrib><creatorcontrib>Rybalova, Tatjana V.</creatorcontrib><creatorcontrib>Gatilov, Yuri V.</creatorcontrib><creatorcontrib>Burdukov, Alexey B.</creatorcontrib><creatorcontrib>Reznikov, Vladimir A.</creatorcontrib><collection>Istex</collection><jtitle>European journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Roshchupkina, Galina A.</au><au>Pervukhina, Natalie V.</au><au>Rybalova, Tatjana V.</au><au>Gatilov, Yuri V.</au><au>Burdukov, Alexey B.</au><au>Reznikov, Vladimir A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides</atitle><jtitle>European journal of organic chemistry</jtitle><addtitle>Eur. J. Org. Chem</addtitle><date>2003-11-14</date><risdate>2003</risdate><volume>2003</volume><issue>22</issue><spage>4432</spage><epage>4437</epage><pages>4432-4437</pages><issn>1434-193X</issn><eissn>1099-0690</eissn><abstract>α‐Imino carbonyl compounds − derivatives of 3‐imidazoline nitroxides − were found to undergo heterocyclization reactions, yielding oxazole and 1,3,5‐triazine derivatives. The most probable course of the reaction was suggested by the radioactive label method. The structures of the heterocycles synthesized were verified by X‐ray analysis of the mixed‐ligand complexes with copper hexafluoroacetylacetonate. (© Wiley‐VCH Verlag GmbH &amp; Co. KGaA, 69451 Weinheim, Germany, 2003)</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/ejoc.200300212</doi><tpages>6</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1434-193X
ispartof European journal of organic chemistry, 2003-11, Vol.2003 (22), p.4432-4437
issn 1434-193X
1099-0690
language eng
recordid cdi_wiley_primary_10_1002_ejoc_200300212_EJOC200300212
source Wiley:Jisc Collections:Wiley Read and Publish Open Access 2024-2025 (reading list)
subjects Heterocycles
Ketones
Luminescence
Nitroxides
Radiochemistry
title Heterocyclization Reaction of α-Imino Carbonyl Compounds − Derivatives of 2,5-Dihydro-1H-imidazole Nitroxides
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-28T03%3A38%3A51IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_wiley&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Heterocyclization%20Reaction%20of%20%CE%B1-Imino%20Carbonyl%20Compounds%20%E2%88%92%20Derivatives%20of%202,5-Dihydro-1H-imidazole%20Nitroxides&rft.jtitle=European%20journal%20of%20organic%20chemistry&rft.au=Roshchupkina,%20Galina%C2%A0A.&rft.date=2003-11-14&rft.volume=2003&rft.issue=22&rft.spage=4432&rft.epage=4437&rft.pages=4432-4437&rft.issn=1434-193X&rft.eissn=1099-0690&rft_id=info:doi/10.1002/ejoc.200300212&rft_dat=%3Cistex_wiley%3Eark_67375_WNG_HZK9SBBW_0%3C/istex_wiley%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-i2412-3c6680cc03e916bec8d0eac04ea47f56cb8aa1a247169150142315761c9c030a3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true