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An Azomethine Ylide Approach to Complex Alkaloid-like Heterocycles
The nitrone above is readily available via the intramolecular aza Diels−Alder reaction of an amino acid derived triene in acetic acid. Subsequent treatment of the nitrone in refluxing toluene with substituted actetylenes produced the pictured pyrrole. At lower temperatures a 2,3-dihydroisoxazole, wh...
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Published in: | Journal of organic chemistry 2007-04, Vol.72 (8), p.3097-3099 |
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container_title | Journal of organic chemistry |
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creator | Murray, William V Francois, David Maden, Amy Turchi, Ignatius |
description | The nitrone above is readily available via the intramolecular aza Diels−Alder reaction of an amino acid derived triene in acetic acid. Subsequent treatment of the nitrone in refluxing toluene with substituted actetylenes produced the pictured pyrrole. At lower temperatures a 2,3-dihydroisoxazole, which is the product of a 3 + 2 dipolar cycloaddition, is produced. Upon heating in refluxing toluene the 2,3-dihydroisoxazole is converted to the pyrrole. |
doi_str_mv | 10.1021/jo062579a |
format | article |
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Subsequent treatment of the nitrone in refluxing toluene with substituted actetylenes produced the pictured pyrrole. At lower temperatures a 2,3-dihydroisoxazole, which is the product of a 3 + 2 dipolar cycloaddition, is produced. Upon heating in refluxing toluene the 2,3-dihydroisoxazole is converted to the pyrrole.</description><identifier>ISSN: 0022-3263</identifier><identifier>EISSN: 1520-6904</identifier><identifier>DOI: 10.1021/jo062579a</identifier><identifier>PMID: 17355150</identifier><identifier>CODEN: JOCEAH</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Alkaloids - chemistry ; Azo Compounds - chemistry ; Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms ; Heterocyclic Compounds, 4 or More Rings - chemistry ; Molecular Structure ; Organic chemistry ; Preparations and properties ; Pyrroles - chemical synthesis ; Pyrroles - chemistry ; Thiosemicarbazones - chemistry</subject><ispartof>Journal of organic chemistry, 2007-04, Vol.72 (8), p.3097-3099</ispartof><rights>Copyright © 2007 American Chemical Society</rights><rights>2007 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a381t-473eb9beb716544750c17b48f795955591c963a4969ba65a6a09705b2fb2ff823</citedby><cites>FETCH-LOGICAL-a381t-473eb9beb716544750c17b48f795955591c963a4969ba65a6a09705b2fb2ff823</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=18695123$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17355150$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Murray, William V</creatorcontrib><creatorcontrib>Francois, David</creatorcontrib><creatorcontrib>Maden, Amy</creatorcontrib><creatorcontrib>Turchi, Ignatius</creatorcontrib><title>An Azomethine Ylide Approach to Complex Alkaloid-like Heterocycles</title><title>Journal of organic chemistry</title><addtitle>J. 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Upon heating in refluxing toluene the 2,3-dihydroisoxazole is converted to the pyrrole.</description><subject>Alkaloids - chemistry</subject><subject>Azo Compounds - chemistry</subject><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms</subject><subject>Heterocyclic Compounds, 4 or More Rings - chemistry</subject><subject>Molecular Structure</subject><subject>Organic chemistry</subject><subject>Preparations and properties</subject><subject>Pyrroles - chemical synthesis</subject><subject>Pyrroles - chemistry</subject><subject>Thiosemicarbazones - chemistry</subject><issn>0022-3263</issn><issn>1520-6904</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNptkE1LAzEQhoMoWqsH_4DsRcHDaj42SXNc6yeIitaDp5BNZ3FtdlOTLai_3kiLvTgMzGEeXh5ehA4IPiWYkrN3jwXlUpkNNCCc4lwoXGyiAcaU5owKtoN2Y3zHaTjn22iHSMY54XiAzssuK799C_1b00H26popZOV8Hryxb1nvs7Fv5w4-s9LNjPPNNHfNDLIb6CF4-2UdxD20VRsXYX91h-jl6nIyvsnvHq5vx-VdbtiI9HkhGVSqgkoSwYtCcmyJrIpRLRVXSUsRqwQzhRKqMoIbYbCSmFe0TluPKBui42VukvtYQOx120QLzpkO_CJqiZnkKmUM0ckStMHHGKDW89C0JnxpgvVvYfqvsMQerkIXVQvTNblqKAFHK8BEa1wdTGebuOZGQnFCWeLyJdfEHj7__ibMtJBJTE8en_XFI5vQ-_MnLda5xsbkswhd6u4fwR--sovN</recordid><startdate>20070413</startdate><enddate>20070413</enddate><creator>Murray, William V</creator><creator>Francois, David</creator><creator>Maden, Amy</creator><creator>Turchi, Ignatius</creator><general>American Chemical Society</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20070413</creationdate><title>An Azomethine Ylide Approach to Complex Alkaloid-like Heterocycles</title><author>Murray, William V ; Francois, David ; Maden, Amy ; Turchi, Ignatius</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a381t-473eb9beb716544750c17b48f795955591c963a4969ba65a6a09705b2fb2ff823</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Alkaloids - chemistry</topic><topic>Azo Compounds - chemistry</topic><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms</topic><topic>Heterocyclic Compounds, 4 or More Rings - chemistry</topic><topic>Molecular Structure</topic><topic>Organic chemistry</topic><topic>Preparations and properties</topic><topic>Pyrroles - chemical synthesis</topic><topic>Pyrroles - chemistry</topic><topic>Thiosemicarbazones - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Murray, William V</creatorcontrib><creatorcontrib>Francois, David</creatorcontrib><creatorcontrib>Maden, Amy</creatorcontrib><creatorcontrib>Turchi, Ignatius</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Murray, William V</au><au>Francois, David</au><au>Maden, Amy</au><au>Turchi, Ignatius</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>An Azomethine Ylide Approach to Complex Alkaloid-like Heterocycles</atitle><jtitle>Journal of organic chemistry</jtitle><addtitle>J. Org. Chem</addtitle><date>2007-04-13</date><risdate>2007</risdate><volume>72</volume><issue>8</issue><spage>3097</spage><epage>3099</epage><pages>3097-3099</pages><issn>0022-3263</issn><eissn>1520-6904</eissn><coden>JOCEAH</coden><abstract>The nitrone above is readily available via the intramolecular aza Diels−Alder reaction of an amino acid derived triene in acetic acid. Subsequent treatment of the nitrone in refluxing toluene with substituted actetylenes produced the pictured pyrrole. At lower temperatures a 2,3-dihydroisoxazole, which is the product of a 3 + 2 dipolar cycloaddition, is produced. Upon heating in refluxing toluene the 2,3-dihydroisoxazole is converted to the pyrrole.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>17355150</pmid><doi>10.1021/jo062579a</doi><tpages>3</tpages></addata></record> |
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subjects | Alkaloids - chemistry Azo Compounds - chemistry Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with n hetero atom and also o and/or s, se, te hetero atoms Heterocyclic Compounds, 4 or More Rings - chemistry Molecular Structure Organic chemistry Preparations and properties Pyrroles - chemical synthesis Pyrroles - chemistry Thiosemicarbazones - chemistry |
title | An Azomethine Ylide Approach to Complex Alkaloid-like Heterocycles |
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