Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones

Abstract We report an easy and powerful approach to the synthesis of novel chromeno[4,3- d ]pyrimidine-5-acetic acids through ANRORC reaction of electron-deficient 3-vinylchromones and 1,3- N , N -binucleophiles. The reaction proceeds under mild conditions (EtOH, rt) and is applicable to a wide rang...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Synthesis (Stuttgart) 2020-01, Vol.52 (1), p.40-50
Hauptverfasser: Chernov, Nikita M., Shutov, Roman V., Potapova, Anastasia E., Yakovlev, Igor P.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 50
container_issue 1
container_start_page 40
container_title Synthesis (Stuttgart)
container_volume 52
creator Chernov, Nikita M.
Shutov, Roman V.
Potapova, Anastasia E.
Yakovlev, Igor P.
description Abstract We report an easy and powerful approach to the synthesis of novel chromeno[4,3- d ]pyrimidine-5-acetic acids through ANRORC reaction of electron-deficient 3-vinylchromones and 1,3- N , N -binucleophiles. The reaction proceeds under mild conditions (EtOH, rt) and is applicable to a wide range of substrates. The described compounds show fluorescence in the violet-blue range (390–460 nm) with Stokes shift of 40–80 nm and moderate quantum yield (0.15–0.20). As the electron-withdrawing group is conserved in the form of an acetic acid fragment, these compounds may readily be functionalized or conjugated to a required substrate for (bio)analytical purposes.
doi_str_mv 10.1055/s-0039-1690723
format Article
fullrecord <record><control><sourceid>thieme_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1055_s_0039_1690723</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1055_s_0039_1690723</sourcerecordid><originalsourceid>FETCH-LOGICAL-c277t-60061aac87af3758302020c4382d75333693606ed984704a67db0bcbef6553dc3</originalsourceid><addsrcrecordid>eNp1kF9LwzAUxYMoOKevPvcDGL1p2qR9lLqpMPDBPwgioUtvXEaXjKQT-u1tt73KfbgP53cOh0PINYNbBnl-FykALykTJciUn5AJy7ikKYPPUzLZS7Io2Dm5iHENMDLlhPxU3v2is-i65LV33QqjjYk3ybzd-YBRj0K1Cn6Dzn9lN5w239s-2I1trMOYmEFJZi3qLnhHH9BYvc_i9MO6vtWj0w_gJTkzdRvx6vin5H0-e6ue6OLl8bm6X1CdStlRASBYXetC1obLvOCQDqczXqSNzDnnouQCBDZlkUnIaiGbJSz1Eo3Ic95oPiW3h1wdfIwBjdoOZevQKwZqnElFNW6hjjMNBnowdCuLG1RrvwtuaPgf_we-vWmv</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones</title><source>Thieme Connect Journals</source><creator>Chernov, Nikita M. ; Shutov, Roman V. ; Potapova, Anastasia E. ; Yakovlev, Igor P.</creator><creatorcontrib>Chernov, Nikita M. ; Shutov, Roman V. ; Potapova, Anastasia E. ; Yakovlev, Igor P.</creatorcontrib><description>Abstract We report an easy and powerful approach to the synthesis of novel chromeno[4,3- d ]pyrimidine-5-acetic acids through ANRORC reaction of electron-deficient 3-vinylchromones and 1,3- N , N -binucleophiles. The reaction proceeds under mild conditions (EtOH, rt) and is applicable to a wide range of substrates. The described compounds show fluorescence in the violet-blue range (390–460 nm) with Stokes shift of 40–80 nm and moderate quantum yield (0.15–0.20). As the electron-withdrawing group is conserved in the form of an acetic acid fragment, these compounds may readily be functionalized or conjugated to a required substrate for (bio)analytical purposes.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-0039-1690723</identifier><language>eng</language><publisher>Stuttgart · New York: Georg Thieme Verlag</publisher><subject>feature</subject><ispartof>Synthesis (Stuttgart), 2020-01, Vol.52 (1), p.40-50</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c277t-60061aac87af3758302020c4382d75333693606ed984704a67db0bcbef6553dc3</citedby><orcidid>0000-0002-7288-0225</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0039-1690723.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-0039-1690723$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3003,3004,27904,27905,54539,54540</link.rule.ids></links><search><creatorcontrib>Chernov, Nikita M.</creatorcontrib><creatorcontrib>Shutov, Roman V.</creatorcontrib><creatorcontrib>Potapova, Anastasia E.</creatorcontrib><creatorcontrib>Yakovlev, Igor P.</creatorcontrib><title>Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract We report an easy and powerful approach to the synthesis of novel chromeno[4,3- d ]pyrimidine-5-acetic acids through ANRORC reaction of electron-deficient 3-vinylchromones and 1,3- N , N -binucleophiles. The reaction proceeds under mild conditions (EtOH, rt) and is applicable to a wide range of substrates. The described compounds show fluorescence in the violet-blue range (390–460 nm) with Stokes shift of 40–80 nm and moderate quantum yield (0.15–0.20). As the electron-withdrawing group is conserved in the form of an acetic acid fragment, these compounds may readily be functionalized or conjugated to a required substrate for (bio)analytical purposes.</description><subject>feature</subject><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp1kF9LwzAUxYMoOKevPvcDGL1p2qR9lLqpMPDBPwgioUtvXEaXjKQT-u1tt73KfbgP53cOh0PINYNbBnl-FykALykTJciUn5AJy7ikKYPPUzLZS7Io2Dm5iHENMDLlhPxU3v2is-i65LV33QqjjYk3ybzd-YBRj0K1Cn6Dzn9lN5w239s-2I1trMOYmEFJZi3qLnhHH9BYvc_i9MO6vtWj0w_gJTkzdRvx6vin5H0-e6ue6OLl8bm6X1CdStlRASBYXetC1obLvOCQDqczXqSNzDnnouQCBDZlkUnIaiGbJSz1Eo3Ic95oPiW3h1wdfIwBjdoOZevQKwZqnElFNW6hjjMNBnowdCuLG1RrvwtuaPgf_we-vWmv</recordid><startdate>20200101</startdate><enddate>20200101</enddate><creator>Chernov, Nikita M.</creator><creator>Shutov, Roman V.</creator><creator>Potapova, Anastasia E.</creator><creator>Yakovlev, Igor P.</creator><general>Georg Thieme Verlag</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-7288-0225</orcidid></search><sort><creationdate>20200101</creationdate><title>Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones</title><author>Chernov, Nikita M. ; Shutov, Roman V. ; Potapova, Anastasia E. ; Yakovlev, Igor P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c277t-60061aac87af3758302020c4382d75333693606ed984704a67db0bcbef6553dc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>feature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chernov, Nikita M.</creatorcontrib><creatorcontrib>Shutov, Roman V.</creatorcontrib><creatorcontrib>Potapova, Anastasia E.</creatorcontrib><creatorcontrib>Yakovlev, Igor P.</creatorcontrib><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chernov, Nikita M.</au><au>Shutov, Roman V.</au><au>Potapova, Anastasia E.</au><au>Yakovlev, Igor P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2020-01-01</date><risdate>2020</risdate><volume>52</volume><issue>1</issue><spage>40</spage><epage>50</epage><pages>40-50</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>Abstract We report an easy and powerful approach to the synthesis of novel chromeno[4,3- d ]pyrimidine-5-acetic acids through ANRORC reaction of electron-deficient 3-vinylchromones and 1,3- N , N -binucleophiles. The reaction proceeds under mild conditions (EtOH, rt) and is applicable to a wide range of substrates. The described compounds show fluorescence in the violet-blue range (390–460 nm) with Stokes shift of 40–80 nm and moderate quantum yield (0.15–0.20). As the electron-withdrawing group is conserved in the form of an acetic acid fragment, these compounds may readily be functionalized or conjugated to a required substrate for (bio)analytical purposes.</abstract><cop>Stuttgart · New York</cop><pub>Georg Thieme Verlag</pub><doi>10.1055/s-0039-1690723</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-7288-0225</orcidid></addata></record>
fulltext fulltext
identifier ISSN: 0039-7881
ispartof Synthesis (Stuttgart), 2020-01, Vol.52 (1), p.40-50
issn 0039-7881
1437-210X
language eng
recordid cdi_crossref_primary_10_1055_s_0039_1690723
source Thieme Connect Journals
subjects feature
title Convenient Synthesis of Fluorescent Chromeno[4,3-d]pyrimidines from Electron-Deficient 3-Vinylchromones
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-21T10%3A13%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-thieme_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Convenient%20Synthesis%20of%20Fluorescent%20Chromeno%5B4,3-d%5Dpyrimidines%20from%20Electron-Deficient%203-Vinylchromones&rft.jtitle=Synthesis%20(Stuttgart)&rft.au=Chernov,%20Nikita%20M.&rft.date=2020-01-01&rft.volume=52&rft.issue=1&rft.spage=40&rft.epage=50&rft.pages=40-50&rft.issn=0039-7881&rft.eissn=1437-210X&rft_id=info:doi/10.1055/s-0039-1690723&rft_dat=%3Cthieme_cross%3E10_1055_s_0039_1690723%3C/thieme_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true