1,3‐Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides and Alkynylbenziodoxoles for Synthesis of Functional Dibenzoullazines
Comprehensive Summary A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the syn...
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| Veröffentlicht in: | Chinese journal of chemistry 2024-05, Vol.42 (10), p.1079-1083 |
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| container_end_page | 1083 |
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| container_issue | 10 |
| container_start_page | 1079 |
| container_title | Chinese journal of chemistry |
| container_volume | 42 |
| creator | Han, Hui Goh, Glen Wee Zhuan Li, Yongxin Yoshikai, Naohiko Ito, Shingo |
| description | Comprehensive Summary
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods. |
| doi_str_mv | 10.1002/cjoc.202300637 |
| format | Article |
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A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.</description><identifier>ISSN: 1001-604X</identifier><identifier>EISSN: 1614-7065</identifier><identifier>DOI: 10.1002/cjoc.202300637</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH & Co. KGaA</publisher><subject>Azomethine ylides ; Cycloaddition ; Dibenzoullazine ; Hypervalent compounds ; Nitrogen heterocycles ; Oxidation ; Synthesis</subject><ispartof>Chinese journal of chemistry, 2024-05, Vol.42 (10), p.1079-1083</ispartof><rights>2024 SIOC, CAS, Shanghai, & WILEY‐VCH GmbH</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c2727-db00165242c69ea6d36242369e6876bd4fa4581d8bfa5e4aa349facafc6f9c243</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%2Fcjoc.202300637$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcjoc.202300637$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Han, Hui</creatorcontrib><creatorcontrib>Goh, Glen Wee Zhuan</creatorcontrib><creatorcontrib>Li, Yongxin</creatorcontrib><creatorcontrib>Yoshikai, Naohiko</creatorcontrib><creatorcontrib>Ito, Shingo</creatorcontrib><title>1,3‐Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides and Alkynylbenziodoxoles for Synthesis of Functional Dibenzoullazines</title><title>Chinese journal of chemistry</title><description>Comprehensive Summary
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.</description><subject>Azomethine ylides</subject><subject>Cycloaddition</subject><subject>Dibenzoullazine</subject><subject>Hypervalent compounds</subject><subject>Nitrogen heterocycles</subject><subject>Oxidation</subject><subject>Synthesis</subject><issn>1001-604X</issn><issn>1614-7065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkDtPwzAUhSMEEqWwMltiJcWxHScdq0B5qFKRAAmmyPFDdXHjYieCdGJm4jfyS3BUBCPTPbr-ztH1iaLjBI4SCNEZX1o-QhBhCCnOdqJBQhMSZ5Cmu0FDmMQUksf96MD7ZeCzDNFB9JGc4q_3z3O9toY5UHTcWCaEbrStgVXg1pqOh6XmYOLsijW92NiVbBa6luDJaCE9YLUAE_Pc1Z2pZL3RVtg3a8KDsg7cdXWzkF77Pm_a1rzPZgac6561rTFsE7L8YbSnmPHy6GcOo4fpxX1xFc_ml9fFZBZzlKEsFlX4Ck0RQZyOJaMC06Bx0DTPaCWIYiTNE5FXiqWSMIbJWDHOFKdqzBHBw-hkm7t29qWVvimXtnXhIl9iiHNMcJ7jQI22FHfWeydVuXZ6xVxXJrDs-y77vsvfvoNhvDW8aiO7f-iyuJkXf95v_JiIlg</recordid><startdate>20240515</startdate><enddate>20240515</enddate><creator>Han, Hui</creator><creator>Goh, Glen Wee Zhuan</creator><creator>Li, Yongxin</creator><creator>Yoshikai, Naohiko</creator><creator>Ito, Shingo</creator><general>WILEY‐VCH Verlag GmbH & Co. KGaA</general><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20240515</creationdate><title>1,3‐Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides and Alkynylbenziodoxoles for Synthesis of Functional Dibenzoullazines</title><author>Han, Hui ; Goh, Glen Wee Zhuan ; Li, Yongxin ; Yoshikai, Naohiko ; Ito, Shingo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2727-db00165242c69ea6d36242369e6876bd4fa4581d8bfa5e4aa349facafc6f9c243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Azomethine ylides</topic><topic>Cycloaddition</topic><topic>Dibenzoullazine</topic><topic>Hypervalent compounds</topic><topic>Nitrogen heterocycles</topic><topic>Oxidation</topic><topic>Synthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Hui</creatorcontrib><creatorcontrib>Goh, Glen Wee Zhuan</creatorcontrib><creatorcontrib>Li, Yongxin</creatorcontrib><creatorcontrib>Yoshikai, Naohiko</creatorcontrib><creatorcontrib>Ito, Shingo</creatorcontrib><collection>CrossRef</collection><jtitle>Chinese journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Han, Hui</au><au>Goh, Glen Wee Zhuan</au><au>Li, Yongxin</au><au>Yoshikai, Naohiko</au><au>Ito, Shingo</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,3‐Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides and Alkynylbenziodoxoles for Synthesis of Functional Dibenzoullazines</atitle><jtitle>Chinese journal of chemistry</jtitle><date>2024-05-15</date><risdate>2024</risdate><volume>42</volume><issue>10</issue><spage>1079</spage><epage>1083</epage><pages>1079-1083</pages><issn>1001-604X</issn><eissn>1614-7065</eissn><abstract>Comprehensive Summary
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.
A new family of dibenzoullazine derivatives was synthesized through 1,3‐dipolar cycloaddition of polycyclic aromatic azomethine ylides with alkynylbenziodoxoles followed by oxidation. The benziodoxole moiety in the resulting products was used as a versatile linchpin for the synthesis of structurally diverse functional dibenzoullazines that are difficult to access by other synthetic methods.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH & Co. KGaA</pub><doi>10.1002/cjoc.202300637</doi><tpages>5</tpages></addata></record> |
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| ispartof | Chinese journal of chemistry, 2024-05, Vol.42 (10), p.1079-1083 |
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| language | eng |
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| source | Wiley Online Library - AutoHoldings Journals |
| subjects | Azomethine ylides Cycloaddition Dibenzoullazine Hypervalent compounds Nitrogen heterocycles Oxidation Synthesis |
| title | 1,3‐Dipolar Cycloaddition of Polycyclic Aromatic Azomethine Ylides and Alkynylbenziodoxoles for Synthesis of Functional Dibenzoullazines |
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