A Convenient Procedure for Transformation of Tertiary Cyclopropanols into 5-Substituted Isoxazoles
Abstract Tertiary cyclopropanols, when treated with an excess of amyl nitrite at room temperature, are smoothly converted into dimeric β-nitrosoketones. Heating the methanolic solutions of the latter under reflux gives 5-substituted isoxazoles in good yields.
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Veröffentlicht in: | Synlett 2006-12, Vol.2006 (20), p.3427-3430 |
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container_title | Synlett |
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creator | Churykau, Dzmitry H. Kulinkovich, Oleg G. |
description | Abstract
Tertiary cyclopropanols, when treated with an excess of amyl nitrite at room temperature, are smoothly converted into dimeric β-nitrosoketones. Heating the methanolic solutions of the latter under reflux gives 5-substituted isoxazoles in good yields. |
doi_str_mv | 10.1055/s-2006-956475 |
format | Article |
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Tertiary cyclopropanols, when treated with an excess of amyl nitrite at room temperature, are smoothly converted into dimeric β-nitrosoketones. Heating the methanolic solutions of the latter under reflux gives 5-substituted isoxazoles in good yields.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLAzEUhYMoWKtL9_kBRpNMMo9lGXwUCgqO65BM7mDKNClJRqy_3il16-pcDh-Xw4fQLaP3jEr5kAintCSNLEUlz9CCiaKaq6Y8RwvaFCWRnIlLdJXSllIm6oYukFnhNvgv8A58xm8x9GCnCHgIEXdR-zQfO51d8DgMuIOYnY4H3B76Mexj2GsfxoSdzwFL8j6ZlF2eMli8TuFb_4QR0jW6GPSY4OYvl-jj6bFrX8jm9Xndrjak55XIpDBDLXTN697Y3gKnkmptmCxLK3VTyIJzY00NVkDNBpDCCmsBGjEwbqWpiiUip799DClFGNQ-ut28VjGqjoJUUkdB6iRo5u9OfP50sAO1DVP088B_8F95oGmX</recordid><startdate>20061218</startdate><enddate>20061218</enddate><creator>Churykau, Dzmitry H.</creator><creator>Kulinkovich, Oleg G.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20061218</creationdate><title>A Convenient Procedure for Transformation of Tertiary Cyclopropanols into 5-Substituted Isoxazoles</title><author>Churykau, Dzmitry H. ; Kulinkovich, Oleg G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-3bf84a828cbdcde2050aab1566d5a935322bdb8ed4e81fe54d4ddee94f12d5b73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Churykau, Dzmitry H.</creatorcontrib><creatorcontrib>Kulinkovich, Oleg G.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Churykau, Dzmitry H.</au><au>Kulinkovich, Oleg G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Convenient Procedure for Transformation of Tertiary Cyclopropanols into 5-Substituted Isoxazoles</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2006-12-18</date><risdate>2006</risdate><volume>2006</volume><issue>20</issue><spage>3427</spage><epage>3430</epage><pages>3427-3430</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
Tertiary cyclopropanols, when treated with an excess of amyl nitrite at room temperature, are smoothly converted into dimeric β-nitrosoketones. Heating the methanolic solutions of the latter under reflux gives 5-substituted isoxazoles in good yields.</abstract><doi>10.1055/s-2006-956475</doi><tpages>4</tpages></addata></record> |
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ispartof | Synlett, 2006-12, Vol.2006 (20), p.3427-3430 |
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language | eng |
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source | Thieme Connect Journals |
subjects | letter |
title | A Convenient Procedure for Transformation of Tertiary Cyclopropanols into 5-Substituted Isoxazoles |
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