Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions
Abstract A rapid synthesis of aryl azides from the corresponding aryl halides catalyzed by CuI/diamine is described. Sodium ascorbate was found to have a positive effect on stabilization of the catalyst system. The reactions were performed under very mild conditions generally with high yields. In th...
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Veröffentlicht in: | Synlett 2005-09, Vol.2005 (14), p.2209-2213 |
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container_title | Synlett |
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creator | Andersen, Jacob Madsen, Ulf Björkling, Fredrik Liang, Xifu |
description | Abstract
A rapid synthesis of aryl azides from the corresponding aryl halides catalyzed by CuI/diamine is described. Sodium ascorbate was found to have a positive effect on stabilization of the catalyst system. The reactions were performed under very mild conditions generally with high yields. In the case of aryl iodides, the transformation could be carried out at room temperature. |
doi_str_mv | 10.1055/s-2005-872248 |
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A rapid synthesis of aryl azides from the corresponding aryl halides catalyzed by CuI/diamine is described. Sodium ascorbate was found to have a positive effect on stabilization of the catalyst system. The reactions were performed under very mild conditions generally with high yields. In the case of aryl iodides, the transformation could be carried out at room temperature.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2005-872248</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2005-09, Vol.2005 (14), p.2209-2213</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-18569842df0f85711edc8d685e648d3958d6f22c309b039cd42120bdaade41743</citedby></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/s-2005-872248.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2005-872248$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>315,781,785,3018,3019,27929,27930,54564,54565</link.rule.ids></links><search><creatorcontrib>Andersen, Jacob</creatorcontrib><creatorcontrib>Madsen, Ulf</creatorcontrib><creatorcontrib>Björkling, Fredrik</creatorcontrib><creatorcontrib>Liang, Xifu</creatorcontrib><title>Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
A rapid synthesis of aryl azides from the corresponding aryl halides catalyzed by CuI/diamine is described. Sodium ascorbate was found to have a positive effect on stabilization of the catalyst system. The reactions were performed under very mild conditions generally with high yields. In the case of aryl iodides, the transformation could be carried out at room temperature.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNp1kMtKAzEUQIMoOFaX7vMBRm9eM8lyKNYKFcHHOkwnCU2ZR0mmi_HrnXbcurrcw-FyOQjdU3ikIOVTIgxAElUwJtQFyqjgxYR0foky0DwnklFxjW5S2gNQoTRkaPVRHYLFn2M37FwKCfcel3FscPkTrEvYx76dwbpqzuTYWRfxW2gsXvadDUPou3SLrnzVJHf3Nxfoe_X8tVyTzfvL67LckJoLGAhVMtdKMOvBK1lQ6mytbK6ky4WyXMtp8YzVHPQWuK6tYJTB1laVdYIWgi8Qme_WsU8pOm8OMbRVHA0Fc4pgkjlFMHOEyX-Y_WEXXOvMvj_GbnrwH_0XeWFcAg</recordid><startdate>20050902</startdate><enddate>20050902</enddate><creator>Andersen, Jacob</creator><creator>Madsen, Ulf</creator><creator>Björkling, Fredrik</creator><creator>Liang, Xifu</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050902</creationdate><title>Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions</title><author>Andersen, Jacob ; Madsen, Ulf ; Björkling, Fredrik ; Liang, Xifu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-18569842df0f85711edc8d685e648d3958d6f22c309b039cd42120bdaade41743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Andersen, Jacob</creatorcontrib><creatorcontrib>Madsen, Ulf</creatorcontrib><creatorcontrib>Björkling, Fredrik</creatorcontrib><creatorcontrib>Liang, Xifu</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Andersen, Jacob</au><au>Madsen, Ulf</au><au>Björkling, Fredrik</au><au>Liang, Xifu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2005-09-02</date><risdate>2005</risdate><volume>2005</volume><issue>14</issue><spage>2209</spage><epage>2213</epage><pages>2209-2213</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
A rapid synthesis of aryl azides from the corresponding aryl halides catalyzed by CuI/diamine is described. Sodium ascorbate was found to have a positive effect on stabilization of the catalyst system. The reactions were performed under very mild conditions generally with high yields. In the case of aryl iodides, the transformation could be carried out at room temperature.</abstract><doi>10.1055/s-2005-872248</doi><tpages>5</tpages></addata></record> |
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title | Rapid Synthesis of Aryl Azides from Aryl Halides under Mild Conditions |
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