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Synthesis of spiropyrans and arylquinones via Ru( ii )-catalyzed condition-controlled coupling of 3-aryl-2 H -benzoxazinones with benzoquinones
Ru( ii )-catalyzed condition-controlled divergent coupling between 3-aryl-2 H -benzoxazin-2-ones and benzoquinones has been realized under operationally simple conditions, affording a series of structurally stable spiropyrans and valuable arylquinones. The potential of this method is also demonstrat...
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Published in: | Chemical communications (Cambridge, England) England), 2023-09, Vol.59 (78), p.11704-11707 |
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Language: | English |
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cites | cdi_FETCH-LOGICAL-c76C-d66c66da750eaf5ba2179c27e88c11148e6c10539d7ab71e42a35eed79f06b013 |
container_end_page | 11707 |
container_issue | 78 |
container_start_page | 11704 |
container_title | Chemical communications (Cambridge, England) |
container_volume | 59 |
creator | Zhang, Mengying He, Yuhao Li, Song Geng, Yuehua Liu, Xiangyang Yang, Xifa |
description | Ru(
ii
)-catalyzed condition-controlled divergent coupling between 3-aryl-2
H
-benzoxazin-2-ones and benzoquinones has been realized under operationally simple conditions, affording a series of structurally stable spiropyrans and valuable arylquinones. The potential of this method is also demonstrated by scale-up synthesis and derivatization. Additionally, an unprecedented cycloruthenated complex has been identified as a key intermediate. |
doi_str_mv | 10.1039/D3CC03395C |
format | article |
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ii
)-catalyzed condition-controlled divergent coupling between 3-aryl-2
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-benzoxazin-2-ones and benzoquinones has been realized under operationally simple conditions, affording a series of structurally stable spiropyrans and valuable arylquinones. The potential of this method is also demonstrated by scale-up synthesis and derivatization. Additionally, an unprecedented cycloruthenated complex has been identified as a key intermediate.</description><identifier>ISSN: 1359-7345</identifier><identifier>EISSN: 1364-548X</identifier><identifier>DOI: 10.1039/D3CC03395C</identifier><language>eng</language><ispartof>Chemical communications (Cambridge, England), 2023-09, Vol.59 (78), p.11704-11707</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c76C-d66c66da750eaf5ba2179c27e88c11148e6c10539d7ab71e42a35eed79f06b013</citedby><cites>FETCH-LOGICAL-c76C-d66c66da750eaf5ba2179c27e88c11148e6c10539d7ab71e42a35eed79f06b013</cites><orcidid>0000-0002-3826-3039</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids></links><search><creatorcontrib>Zhang, Mengying</creatorcontrib><creatorcontrib>He, Yuhao</creatorcontrib><creatorcontrib>Li, Song</creatorcontrib><creatorcontrib>Geng, Yuehua</creatorcontrib><creatorcontrib>Liu, Xiangyang</creatorcontrib><creatorcontrib>Yang, Xifa</creatorcontrib><title>Synthesis of spiropyrans and arylquinones via Ru( ii )-catalyzed condition-controlled coupling of 3-aryl-2 H -benzoxazinones with benzoquinones</title><title>Chemical communications (Cambridge, England)</title><description>Ru(
ii
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ii
)-catalyzed condition-controlled divergent coupling between 3-aryl-2
H
-benzoxazin-2-ones and benzoquinones has been realized under operationally simple conditions, affording a series of structurally stable spiropyrans and valuable arylquinones. The potential of this method is also demonstrated by scale-up synthesis and derivatization. Additionally, an unprecedented cycloruthenated complex has been identified as a key intermediate.</abstract><doi>10.1039/D3CC03395C</doi><tpages>4</tpages><orcidid>https://orcid.org/0000-0002-3826-3039</orcidid></addata></record> |
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ispartof | Chemical communications (Cambridge, England), 2023-09, Vol.59 (78), p.11704-11707 |
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language | eng |
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source | Royal Society of Chemistry |
title | Synthesis of spiropyrans and arylquinones via Ru( ii )-catalyzed condition-controlled coupling of 3-aryl-2 H -benzoxazinones with benzoquinones |
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