1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles
The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J....
Gespeichert in:
| Veröffentlicht in: | Journal of heterocyclic chemistry 2011-07, Vol.48 (4), p.824-828 |
|---|---|
| Hauptverfasser: | , , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 828 |
|---|---|
| container_issue | 4 |
| container_start_page | 824 |
| container_title | Journal of heterocyclic chemistry |
| container_volume | 48 |
| creator | Starosotnikov, Alexey M. Bastrakov, Maxim A. Pechenkin, Sergey Yu Leontieva, Margarita A. Kachala, Vadim V. Shevelev, Svyatoslav A. |
| description | The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J. Heterocyclic Chem., (2011). |
| doi_str_mv | 10.1002/jhet.599 |
| format | Article |
| fullrecord | <record><control><sourceid>istex_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_jhet_599</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>ark_67375_WNG_V4KVCDS3_8</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3039-917ee1cb4b250339ab1de8cb77c1e70a80267296e9aec4f233d78f98479ff6333</originalsourceid><addsrcrecordid>eNp1kD1PwzAQhi0EEqUg8RM8MpBix0kdj6gtLR8qA6WwWY5zUV3cuIqNSvrrSVSExMB0d-89d8OD0CUlA0pIfLNeQRikQhyhHhUJi1Iq2DHqtas4omn8forOvF-3I2Wc95Ch1ywam62zqsa60dapojDBuAq7En9WPqjcWLOHAs-jDYRVY7Hau64zFeDGmgJwcLgyoXY5VHtoU1VVYFVob3YmrDregj9HJ6WyHi5-ah-93k0Wo1n09Dy9H90-RZoRJiJBOQDVeZLHKWFMqJwWkOmcc02BE5WReMhjMQShQCdlzFjBs1JkCRdlOWSM9dHV4a-unfc1lHJbm42qG0mJ7BTJTpFsFbVodEB3xkLzLycfZpPFH974AF-_vKo_5JAznsq3-VQuk8flaPzCZMa-ARVjeV4</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles</title><source>Access via Wiley Online Library</source><creator>Starosotnikov, Alexey M. ; Bastrakov, Maxim A. ; Pechenkin, Sergey Yu ; Leontieva, Margarita A. ; Kachala, Vadim V. ; Shevelev, Svyatoslav A.</creator><creatorcontrib>Starosotnikov, Alexey M. ; Bastrakov, Maxim A. ; Pechenkin, Sergey Yu ; Leontieva, Margarita A. ; Kachala, Vadim V. ; Shevelev, Svyatoslav A.</creatorcontrib><description>The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J. Heterocyclic Chem., (2011).</description><identifier>ISSN: 0022-152X</identifier><identifier>EISSN: 1943-5193</identifier><identifier>DOI: 10.1002/jhet.599</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><ispartof>Journal of heterocyclic chemistry, 2011-07, Vol.48 (4), p.824-828</ispartof><rights>Copyright © 2011 HeteroCorporation</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3039-917ee1cb4b250339ab1de8cb77c1e70a80267296e9aec4f233d78f98479ff6333</citedby><cites>FETCH-LOGICAL-c3039-917ee1cb4b250339ab1de8cb77c1e70a80267296e9aec4f233d78f98479ff6333</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%2Fjhet.599$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjhet.599$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Starosotnikov, Alexey M.</creatorcontrib><creatorcontrib>Bastrakov, Maxim A.</creatorcontrib><creatorcontrib>Pechenkin, Sergey Yu</creatorcontrib><creatorcontrib>Leontieva, Margarita A.</creatorcontrib><creatorcontrib>Kachala, Vadim V.</creatorcontrib><creatorcontrib>Shevelev, Svyatoslav A.</creatorcontrib><title>1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles</title><title>Journal of heterocyclic chemistry</title><addtitle>J. Heterocyclic Chem</addtitle><description>The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J. Heterocyclic Chem., (2011).</description><issn>0022-152X</issn><issn>1943-5193</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp1kD1PwzAQhi0EEqUg8RM8MpBix0kdj6gtLR8qA6WwWY5zUV3cuIqNSvrrSVSExMB0d-89d8OD0CUlA0pIfLNeQRikQhyhHhUJi1Iq2DHqtas4omn8forOvF-3I2Wc95Ch1ywam62zqsa60dapojDBuAq7En9WPqjcWLOHAs-jDYRVY7Hau64zFeDGmgJwcLgyoXY5VHtoU1VVYFVob3YmrDregj9HJ6WyHi5-ah-93k0Wo1n09Dy9H90-RZoRJiJBOQDVeZLHKWFMqJwWkOmcc02BE5WReMhjMQShQCdlzFjBs1JkCRdlOWSM9dHV4a-unfc1lHJbm42qG0mJ7BTJTpFsFbVodEB3xkLzLycfZpPFH974AF-_vKo_5JAznsq3-VQuk8flaPzCZMa-ARVjeV4</recordid><startdate>201107</startdate><enddate>201107</enddate><creator>Starosotnikov, Alexey M.</creator><creator>Bastrakov, Maxim A.</creator><creator>Pechenkin, Sergey Yu</creator><creator>Leontieva, Margarita A.</creator><creator>Kachala, Vadim V.</creator><creator>Shevelev, Svyatoslav A.</creator><general>John Wiley & Sons, Inc</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>201107</creationdate><title>1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles</title><author>Starosotnikov, Alexey M. ; Bastrakov, Maxim A. ; Pechenkin, Sergey Yu ; Leontieva, Margarita A. ; Kachala, Vadim V. ; Shevelev, Svyatoslav A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3039-917ee1cb4b250339ab1de8cb77c1e70a80267296e9aec4f233d78f98479ff6333</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Starosotnikov, Alexey M.</creatorcontrib><creatorcontrib>Bastrakov, Maxim A.</creatorcontrib><creatorcontrib>Pechenkin, Sergey Yu</creatorcontrib><creatorcontrib>Leontieva, Margarita A.</creatorcontrib><creatorcontrib>Kachala, Vadim V.</creatorcontrib><creatorcontrib>Shevelev, Svyatoslav A.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Journal of heterocyclic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Starosotnikov, Alexey M.</au><au>Bastrakov, Maxim A.</au><au>Pechenkin, Sergey Yu</au><au>Leontieva, Margarita A.</au><au>Kachala, Vadim V.</au><au>Shevelev, Svyatoslav A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles</atitle><jtitle>Journal of heterocyclic chemistry</jtitle><addtitle>J. Heterocyclic Chem</addtitle><date>2011-07</date><risdate>2011</risdate><volume>48</volume><issue>4</issue><spage>824</spage><epage>828</epage><pages>824-828</pages><issn>0022-152X</issn><eissn>1943-5193</eissn><abstract>The 1,3‐dipolar cycloaddition of unstabilized N‐methyl azomethine ylide to mononitro benzazoles was studied. Depending on the nature of substituents and annelated azoles, the reaction affords previously unknown isoindole fused heterocyclic systems. The reactivity of the cycloadducts was examined. J. Heterocyclic Chem., (2011).</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><doi>10.1002/jhet.599</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0022-152X |
| ispartof | Journal of heterocyclic chemistry, 2011-07, Vol.48 (4), p.824-828 |
| issn | 0022-152X 1943-5193 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_jhet_599 |
| source | Access via Wiley Online Library |
| title | 1,3-Dipolar cycloaddition of unstabilized N-methyl azomethine ylide to nitrobenzene annelated with azoles |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T18%3A04%3A59IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-istex_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=1,3-Dipolar%20cycloaddition%20of%20unstabilized%20N-methyl%20azomethine%20ylide%20to%20nitrobenzene%20annelated%20with%20azoles&rft.jtitle=Journal%20of%20heterocyclic%20chemistry&rft.au=Starosotnikov,%20Alexey%20M.&rft.date=2011-07&rft.volume=48&rft.issue=4&rft.spage=824&rft.epage=828&rft.pages=824-828&rft.issn=0022-152X&rft.eissn=1943-5193&rft_id=info:doi/10.1002/jhet.599&rft_dat=%3Cistex_cross%3Eark_67375_WNG_V4KVCDS3_8%3C/istex_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 |