Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones
This article describes the synthesis of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1 Н )-ones and provides details of their reactivity, such as nucleophilic and electrophilic substitution, as well as associated processes: acidic degradation, isomerization, and diazine ring cleavage.
Gespeichert in:
Veröffentlicht in: | Chemistry of heterocyclic compounds (New York, N.Y. 1965) N.Y. 1965), 2019-05, Vol.55 (4-5), p.307-311 |
---|---|
Hauptverfasser: | , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 311 |
---|---|
container_issue | 4-5 |
container_start_page | 307 |
container_title | Chemistry of heterocyclic compounds (New York, N.Y. 1965) |
container_volume | 55 |
creator | Yavolovskii, Arkadii A. Grishchuk, Lidiya V. Ivanov, Yurii E. Pluzhnik-Gladyr, Sergei M. Kamalov, Gerbert L. |
description | This article describes the synthesis of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1
Н
)-ones and provides details of their reactivity, such as nucleophilic and electrophilic substitution, as well as associated processes: acidic degradation, isomerization, and diazine ring cleavage. |
doi_str_mv | 10.1007/s10593-019-02459-9 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2239742753</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2239742753</sourcerecordid><originalsourceid>FETCH-LOGICAL-c363t-72748500dcbf6380793f037a73758fccd6a9c1ef6cde317ad206ece2def534613</originalsourceid><addsrcrecordid>eNp9kM1KAzEUhYMoWKsv4GrATQtGk9zJZLKU4h8UXKjrEPNjp7RJTabgPIzv5CMZreDO1eXCOefe8yF0SskFJURcZkq4BEyoxITVXGK5h0aUC8AtcNhHI0KIxEAZO0RHOS_LKmhbj5B9HEK_cLnLlQ626pMO2ce01n0XQ-Wd7rfJ5Sr6iuEJw_E9YoZ1GlauXwyrzrrgppidA7bdYrApbobUrTvbBVxP6OfHFMfg8jE68HqV3cnvHKPnm-un2R2eP9zez67m2EADPRZM1C0nxJoX30BLhARPQGgBgrfeGNtoaajzjbEOqNCWkcYZx6zzHOqGwhid7XI3Kb5tXe7VMm5TKCcVYyBFzQSHomI7lUkx5-S82pSfSydFifqmqXY0VaGpfmgqWUywM-UiDq8u_UX_4_oCGVJ31w</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2239742753</pqid></control><display><type>article</type><title>Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones</title><source>SpringerLink Journals - AutoHoldings</source><creator>Yavolovskii, Arkadii A. ; Grishchuk, Lidiya V. ; Ivanov, Yurii E. ; Pluzhnik-Gladyr, Sergei M. ; Kamalov, Gerbert L.</creator><creatorcontrib>Yavolovskii, Arkadii A. ; Grishchuk, Lidiya V. ; Ivanov, Yurii E. ; Pluzhnik-Gladyr, Sergei M. ; Kamalov, Gerbert L.</creatorcontrib><description>This article describes the synthesis of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1
Н
)-ones and provides details of their reactivity, such as nucleophilic and electrophilic substitution, as well as associated processes: acidic degradation, isomerization, and diazine ring cleavage.</description><identifier>ISSN: 0009-3122</identifier><identifier>EISSN: 1573-8353</identifier><identifier>DOI: 10.1007/s10593-019-02459-9</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Chemistry ; Chemistry and Materials Science ; Isomerization ; Organic Chemistry ; Pharmacy ; Synthesis</subject><ispartof>Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2019-05, Vol.55 (4-5), p.307-311</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2019</rights><rights>Copyright Springer Nature B.V. 2019</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-72748500dcbf6380793f037a73758fccd6a9c1ef6cde317ad206ece2def534613</citedby><cites>FETCH-LOGICAL-c363t-72748500dcbf6380793f037a73758fccd6a9c1ef6cde317ad206ece2def534613</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10593-019-02459-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10593-019-02459-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>315,781,785,27925,27926,41489,42558,51320</link.rule.ids></links><search><creatorcontrib>Yavolovskii, Arkadii A.</creatorcontrib><creatorcontrib>Grishchuk, Lidiya V.</creatorcontrib><creatorcontrib>Ivanov, Yurii E.</creatorcontrib><creatorcontrib>Pluzhnik-Gladyr, Sergei M.</creatorcontrib><creatorcontrib>Kamalov, Gerbert L.</creatorcontrib><title>Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones</title><title>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</title><addtitle>Chem Heterocycl Comp</addtitle><description>This article describes the synthesis of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1
Н
)-ones and provides details of their reactivity, such as nucleophilic and electrophilic substitution, as well as associated processes: acidic degradation, isomerization, and diazine ring cleavage.</description><subject>Chemistry</subject><subject>Chemistry and Materials Science</subject><subject>Isomerization</subject><subject>Organic Chemistry</subject><subject>Pharmacy</subject><subject>Synthesis</subject><issn>0009-3122</issn><issn>1573-8353</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kM1KAzEUhYMoWKsv4GrATQtGk9zJZLKU4h8UXKjrEPNjp7RJTabgPIzv5CMZreDO1eXCOefe8yF0SskFJURcZkq4BEyoxITVXGK5h0aUC8AtcNhHI0KIxEAZO0RHOS_LKmhbj5B9HEK_cLnLlQ626pMO2ce01n0XQ-Wd7rfJ5Sr6iuEJw_E9YoZ1GlauXwyrzrrgppidA7bdYrApbobUrTvbBVxP6OfHFMfg8jE68HqV3cnvHKPnm-un2R2eP9zez67m2EADPRZM1C0nxJoX30BLhARPQGgBgrfeGNtoaajzjbEOqNCWkcYZx6zzHOqGwhid7XI3Kb5tXe7VMm5TKCcVYyBFzQSHomI7lUkx5-S82pSfSydFifqmqXY0VaGpfmgqWUywM-UiDq8u_UX_4_oCGVJ31w</recordid><startdate>20190515</startdate><enddate>20190515</enddate><creator>Yavolovskii, Arkadii A.</creator><creator>Grishchuk, Lidiya V.</creator><creator>Ivanov, Yurii E.</creator><creator>Pluzhnik-Gladyr, Sergei M.</creator><creator>Kamalov, Gerbert L.</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20190515</creationdate><title>Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones</title><author>Yavolovskii, Arkadii A. ; Grishchuk, Lidiya V. ; Ivanov, Yurii E. ; Pluzhnik-Gladyr, Sergei M. ; Kamalov, Gerbert L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-72748500dcbf6380793f037a73758fccd6a9c1ef6cde317ad206ece2def534613</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Chemistry</topic><topic>Chemistry and Materials Science</topic><topic>Isomerization</topic><topic>Organic Chemistry</topic><topic>Pharmacy</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yavolovskii, Arkadii A.</creatorcontrib><creatorcontrib>Grishchuk, Lidiya V.</creatorcontrib><creatorcontrib>Ivanov, Yurii E.</creatorcontrib><creatorcontrib>Pluzhnik-Gladyr, Sergei M.</creatorcontrib><creatorcontrib>Kamalov, Gerbert L.</creatorcontrib><collection>CrossRef</collection><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yavolovskii, Arkadii A.</au><au>Grishchuk, Lidiya V.</au><au>Ivanov, Yurii E.</au><au>Pluzhnik-Gladyr, Sergei M.</au><au>Kamalov, Gerbert L.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones</atitle><jtitle>Chemistry of heterocyclic compounds (New York, N.Y. 1965)</jtitle><stitle>Chem Heterocycl Comp</stitle><date>2019-05-15</date><risdate>2019</risdate><volume>55</volume><issue>4-5</issue><spage>307</spage><epage>311</epage><pages>307-311</pages><issn>0009-3122</issn><eissn>1573-8353</eissn><abstract>This article describes the synthesis of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1
Н
)-ones and provides details of their reactivity, such as nucleophilic and electrophilic substitution, as well as associated processes: acidic degradation, isomerization, and diazine ring cleavage.</abstract><cop>New York</cop><pub>Springer US</pub><doi>10.1007/s10593-019-02459-9</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0009-3122 |
ispartof | Chemistry of heterocyclic compounds (New York, N.Y. 1965), 2019-05, Vol.55 (4-5), p.307-311 |
issn | 0009-3122 1573-8353 |
language | eng |
recordid | cdi_proquest_journals_2239742753 |
source | SpringerLink Journals - AutoHoldings |
subjects | Chemistry Chemistry and Materials Science Isomerization Organic Chemistry Pharmacy Synthesis |
title | Synthesis and transformation features of 2-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1Н)-ones |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-18T15%3A13%3A32IST&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=Synthesis%20and%20transformation%20features%20of%202-(2-oxo-2-arylethylidene)-2,3-dihydropyrimidin-4(1%D0%9D)-ones&rft.jtitle=Chemistry%20of%20heterocyclic%20compounds%20(New%20York,%20N.Y.%201965)&rft.au=Yavolovskii,%20Arkadii%20A.&rft.date=2019-05-15&rft.volume=55&rft.issue=4-5&rft.spage=307&rft.epage=311&rft.pages=307-311&rft.issn=0009-3122&rft.eissn=1573-8353&rft_id=info:doi/10.1007/s10593-019-02459-9&rft_dat=%3Cproquest_cross%3E2239742753%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2239742753&rft_id=info:pmid/&rfr_iscdi=true |