Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines
A Rh‐catalyzed unique and direct approach for constructing a series of 5‐arylimidazo[1,2‐c]quinazolines in moderate to excellent yields from simple and readily available 2‐arylimidazoles and 3‐phenyl‐1,4,2‐dioxazol‐5‐ones was described. This procedure proceeds with sequential ortho‐C−H bond amidatio...
Gespeichert in:
Veröffentlicht in: | Advanced synthesis & catalysis 2018-03, Vol.360 (6), p.1111-1115 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 1115 |
---|---|
container_issue | 6 |
container_start_page | 1111 |
container_title | Advanced synthesis & catalysis |
container_volume | 360 |
creator | Wu, Xiaopeng Sun, Song Xu, Shengbo Cheng, Jiang |
description | A Rh‐catalyzed unique and direct approach for constructing a series of 5‐arylimidazo[1,2‐c]quinazolines in moderate to excellent yields from simple and readily available 2‐arylimidazoles and 3‐phenyl‐1,4,2‐dioxazol‐5‐ones was described. This procedure proceeds with sequential ortho‐C−H bond amidation and cyclization, which represents a facile and straightforward pathway to access such frameworks. |
doi_str_mv | 10.1002/adsc.201701331 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_2017688800</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2017688800</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3541-7092dba14b7cf65cbb8310d088d35d3e841f41279670ea4dcc678c15c34a83933</originalsourceid><addsrcrecordid>eNqFkM9LwzAYhosoOKdXzwWv68zX9Ed6rJ06YSD44yRS0qRlGV2zJS2zO3n0KPof7i8xdTLx5CHk4_2eJ4HXsk4BDQEh95xyzYYughABxrBn9SAA3_EgiPZ3s48OrSOtZ8hgJAx71ufddPP6ntCalu0653ZcVU1JayErWxa2VPVUdvvN28fYvpAV113smihWbSnmgtO1LHNtr0Q9tWHgDbrdSMiXLjejb46sDFDLFVXc9v-qT_AtsOdlI6pOEYY9tg4KWur85OfuW49Xlw_J2JncXt8k8cRh2PfACVHk8oyCl4WsCHyWZQQD4ogQjn2Oc-JB4YEbRkGIcupxxoKQMPAZ9ijBEcZ962z77kLJZZPrOp3JRlXmy7SrMSCEIGSo4ZZiSmqt8iJdKDGnqk0BpV3xaVd8uiveCNFWWIkyb_-h03h0n_y6X5v0kBs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2017688800</pqid></control><display><type>article</type><title>Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines</title><source>Wiley Online Library All Journals</source><creator>Wu, Xiaopeng ; Sun, Song ; Xu, Shengbo ; Cheng, Jiang</creator><creatorcontrib>Wu, Xiaopeng ; Sun, Song ; Xu, Shengbo ; Cheng, Jiang</creatorcontrib><description>A Rh‐catalyzed unique and direct approach for constructing a series of 5‐arylimidazo[1,2‐c]quinazolines in moderate to excellent yields from simple and readily available 2‐arylimidazoles and 3‐phenyl‐1,4,2‐dioxazol‐5‐ones was described. This procedure proceeds with sequential ortho‐C−H bond amidation and cyclization, which represents a facile and straightforward pathway to access such frameworks.</description><identifier>ISSN: 1615-4150</identifier><identifier>EISSN: 1615-4169</identifier><identifier>DOI: 10.1002/adsc.201701331</identifier><language>eng</language><publisher>Heidelberg: Wiley Subscription Services, Inc</publisher><subject>amidation ; annulation ; Chemical reactions ; dioxazolones ; Hydrogen bonds ; Organic chemistry ; quinazolines ; Rhodium catalysis</subject><ispartof>Advanced synthesis & catalysis, 2018-03, Vol.360 (6), p.1111-1115</ispartof><rights>2018 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3541-7092dba14b7cf65cbb8310d088d35d3e841f41279670ea4dcc678c15c34a83933</citedby><cites>FETCH-LOGICAL-c3541-7092dba14b7cf65cbb8310d088d35d3e841f41279670ea4dcc678c15c34a83933</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fadsc.201701331$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fadsc.201701331$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45573,45574</link.rule.ids></links><search><creatorcontrib>Wu, Xiaopeng</creatorcontrib><creatorcontrib>Sun, Song</creatorcontrib><creatorcontrib>Xu, Shengbo</creatorcontrib><creatorcontrib>Cheng, Jiang</creatorcontrib><title>Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines</title><title>Advanced synthesis & catalysis</title><description>A Rh‐catalyzed unique and direct approach for constructing a series of 5‐arylimidazo[1,2‐c]quinazolines in moderate to excellent yields from simple and readily available 2‐arylimidazoles and 3‐phenyl‐1,4,2‐dioxazol‐5‐ones was described. This procedure proceeds with sequential ortho‐C−H bond amidation and cyclization, which represents a facile and straightforward pathway to access such frameworks.</description><subject>amidation</subject><subject>annulation</subject><subject>Chemical reactions</subject><subject>dioxazolones</subject><subject>Hydrogen bonds</subject><subject>Organic chemistry</subject><subject>quinazolines</subject><subject>Rhodium catalysis</subject><issn>1615-4150</issn><issn>1615-4169</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LwzAYhosoOKdXzwWv68zX9Ed6rJ06YSD44yRS0qRlGV2zJS2zO3n0KPof7i8xdTLx5CHk4_2eJ4HXsk4BDQEh95xyzYYughABxrBn9SAA3_EgiPZ3s48OrSOtZ8hgJAx71ufddPP6ntCalu0653ZcVU1JayErWxa2VPVUdvvN28fYvpAV113smihWbSnmgtO1LHNtr0Q9tWHgDbrdSMiXLjejb46sDFDLFVXc9v-qT_AtsOdlI6pOEYY9tg4KWur85OfuW49Xlw_J2JncXt8k8cRh2PfACVHk8oyCl4WsCHyWZQQD4ogQjn2Oc-JB4YEbRkGIcupxxoKQMPAZ9ijBEcZ962z77kLJZZPrOp3JRlXmy7SrMSCEIGSo4ZZiSmqt8iJdKDGnqk0BpV3xaVd8uiveCNFWWIkyb_-h03h0n_y6X5v0kBs</recordid><startdate>20180320</startdate><enddate>20180320</enddate><creator>Wu, Xiaopeng</creator><creator>Sun, Song</creator><creator>Xu, Shengbo</creator><creator>Cheng, Jiang</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8FD</scope><scope>L7M</scope></search><sort><creationdate>20180320</creationdate><title>Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines</title><author>Wu, Xiaopeng ; Sun, Song ; Xu, Shengbo ; Cheng, Jiang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3541-7092dba14b7cf65cbb8310d088d35d3e841f41279670ea4dcc678c15c34a83933</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>amidation</topic><topic>annulation</topic><topic>Chemical reactions</topic><topic>dioxazolones</topic><topic>Hydrogen bonds</topic><topic>Organic chemistry</topic><topic>quinazolines</topic><topic>Rhodium catalysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wu, Xiaopeng</creatorcontrib><creatorcontrib>Sun, Song</creatorcontrib><creatorcontrib>Xu, Shengbo</creatorcontrib><creatorcontrib>Cheng, Jiang</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Technology Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced synthesis & catalysis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wu, Xiaopeng</au><au>Sun, Song</au><au>Xu, Shengbo</au><au>Cheng, Jiang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines</atitle><jtitle>Advanced synthesis & catalysis</jtitle><date>2018-03-20</date><risdate>2018</risdate><volume>360</volume><issue>6</issue><spage>1111</spage><epage>1115</epage><pages>1111-1115</pages><issn>1615-4150</issn><eissn>1615-4169</eissn><abstract>A Rh‐catalyzed unique and direct approach for constructing a series of 5‐arylimidazo[1,2‐c]quinazolines in moderate to excellent yields from simple and readily available 2‐arylimidazoles and 3‐phenyl‐1,4,2‐dioxazol‐5‐ones was described. This procedure proceeds with sequential ortho‐C−H bond amidation and cyclization, which represents a facile and straightforward pathway to access such frameworks.</abstract><cop>Heidelberg</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/adsc.201701331</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1615-4150 |
ispartof | Advanced synthesis & catalysis, 2018-03, Vol.360 (6), p.1111-1115 |
issn | 1615-4150 1615-4169 |
language | eng |
recordid | cdi_proquest_journals_2017688800 |
source | Wiley Online Library All Journals |
subjects | amidation annulation Chemical reactions dioxazolones Hydrogen bonds Organic chemistry quinazolines Rhodium catalysis |
title | Rh‐Catalyzed Annulation of ortho‐C−H Bonds of 2‐Arylimidazoles with 1,4,2‐Dioxazol‐5‐ones toward 5‐Arylimidazo[1,2‐c]quinazolines |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-09T01%3A51%3A49IST&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=Rh%E2%80%90Catalyzed%20Annulation%20of%20ortho%E2%80%90C%E2%88%92H%20Bonds%20of%202%E2%80%90Arylimidazoles%20with%201,4,2%E2%80%90Dioxazol%E2%80%905%E2%80%90ones%20toward%205%E2%80%90Arylimidazo%5B1,2%E2%80%90c%5Dquinazolines&rft.jtitle=Advanced%20synthesis%20&%20catalysis&rft.au=Wu,%20Xiaopeng&rft.date=2018-03-20&rft.volume=360&rft.issue=6&rft.spage=1111&rft.epage=1115&rft.pages=1111-1115&rft.issn=1615-4150&rft.eissn=1615-4169&rft_id=info:doi/10.1002/adsc.201701331&rft_dat=%3Cproquest_cross%3E2017688800%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=2017688800&rft_id=info:pmid/&rfr_iscdi=true |