Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion
Abstract We reported here a facile synthesis of dibenzo[ a , e ]cyclooctene-5,11(6 H ,12 H )-diones via dimerization of benzocyclobutenones in the presence of simple base via the elusive benzocyclobutenone anion. The temperature effect played a crucial role in the dimerization reaction. Further s...
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Veröffentlicht in: | Synthesis (Stuttgart) 2021-12, Vol.53 (23), p.4477-4483 |
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container_title | Synthesis (Stuttgart) |
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creator | Huang, Yingchao Chen, Jun Liu, Yu Lu, Ping |
description | Abstract
We reported here a facile synthesis of dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones via dimerization of benzocyclobutenones in the presence of simple base via the elusive benzocyclobutenone anion. The temperature effect played a crucial role in the dimerization reaction. Further synthesis of 5,11-disubstituted dibenzo[
a
,
e
]cyclooctenes (dibenzo[
a
,
e
][8]annulenes) from dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones was also explored. |
doi_str_mv | 10.1055/a-1545-7706 |
format | Article |
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We reported here a facile synthesis of dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones via dimerization of benzocyclobutenones in the presence of simple base via the elusive benzocyclobutenone anion. The temperature effect played a crucial role in the dimerization reaction. Further synthesis of 5,11-disubstituted dibenzo[
a
,
e
]cyclooctenes (dibenzo[
a
,
e
][8]annulenes) from dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones was also explored.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/a-1545-7706</identifier><language>eng</language><publisher>Rüdigerstraße 14, 70469 Stuttgart, Germany: Georg Thieme Verlag KG</publisher><ispartof>Synthesis (Stuttgart), 2021-12, Vol.53 (23), p.4477-4483</ispartof><rights>Thieme. All rights reserved</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c268t-c64c7190cf435bbbb8c47cba42526e8e8e39447b7897430f40e0956d34c497d93</citedby><cites>FETCH-LOGICAL-c268t-c64c7190cf435bbbb8c47cba42526e8e8e39447b7897430f40e0956d34c497d93</cites><orcidid>0000-0002-2259-2700</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/a-1545-7706.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/a-1545-7706$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Huang, Yingchao</creatorcontrib><creatorcontrib>Chen, Jun</creatorcontrib><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Lu, Ping</creatorcontrib><title>Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>Abstract
We reported here a facile synthesis of dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones via dimerization of benzocyclobutenones in the presence of simple base via the elusive benzocyclobutenone anion. The temperature effect played a crucial role in the dimerization reaction. Further synthesis of 5,11-disubstituted dibenzo[
a
,
e
]cyclooctenes (dibenzo[
a
,
e
][8]annulenes) from dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones was also explored.</description><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNptkE1LAzEQhoMoWKsn_0COfjQ62SSbzbHWaoWCBxUEkZBNszSl3chmt1B_vVnr0XkPc3meYXgROqdwQ0GIW0Oo4IJICfkBGlDOJMkovB-iAQBTRBYFPUYnMa4AQGZMDZB52dXt0kUfcajwvS9d_R0-zMh92p1dh2BbVzsiRpRe5LMRzWaXZOFD7SLeeoOTiafrLvqtw3e9-SuVXZISg8d1Qk_RUWXW0Z397SF6e5i-TmZk_vz4NBnPic3yoiU251ZSBbbiTJRpCsulLQ3PRJa7IoUpzmUpCyU5g4qDAyXyBeOWK7lQbIiu93dtE2JsXKW_Gr8xzU5T0H072ui-Hd23k-irPd0uvds4vQpdU6f3_oV_APtKZAA</recordid><startdate>20211201</startdate><enddate>20211201</enddate><creator>Huang, Yingchao</creator><creator>Chen, Jun</creator><creator>Liu, Yu</creator><creator>Lu, Ping</creator><general>Georg Thieme Verlag KG</general><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0002-2259-2700</orcidid></search><sort><creationdate>20211201</creationdate><title>Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion</title><author>Huang, Yingchao ; Chen, Jun ; Liu, Yu ; Lu, Ping</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c268t-c64c7190cf435bbbb8c47cba42526e8e8e39447b7897430f40e0956d34c497d93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Yingchao</creatorcontrib><creatorcontrib>Chen, Jun</creatorcontrib><creatorcontrib>Liu, Yu</creatorcontrib><creatorcontrib>Lu, Ping</creatorcontrib><collection>CrossRef</collection><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Yingchao</au><au>Chen, Jun</au><au>Liu, Yu</au><au>Lu, Ping</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2021-12-01</date><risdate>2021</risdate><volume>53</volume><issue>23</issue><spage>4477</spage><epage>4483</epage><pages>4477-4483</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>Abstract
We reported here a facile synthesis of dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones via dimerization of benzocyclobutenones in the presence of simple base via the elusive benzocyclobutenone anion. The temperature effect played a crucial role in the dimerization reaction. Further synthesis of 5,11-disubstituted dibenzo[
a
,
e
]cyclooctenes (dibenzo[
a
,
e
][8]annulenes) from dibenzo[
a
,
e
]cyclooctene-5,11(6
H
,12
H
)-diones was also explored.</abstract><cop>Rüdigerstraße 14, 70469 Stuttgart, Germany</cop><pub>Georg Thieme Verlag KG</pub><doi>10.1055/a-1545-7706</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2259-2700</orcidid></addata></record> |
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ispartof | Synthesis (Stuttgart), 2021-12, Vol.53 (23), p.4477-4483 |
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language | eng |
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source | Thieme - Connect here FIRST to enable access |
title | Synthesis of Dibenzo[a,e]cyclooctene-5,11(6H,12H)-diones via the Elusive Benzocyclobutenone Anion |
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