ENCHAINEMENTS HETEROATOMIQUES ET LEURS PRODUITS DE CYCLISATION‒IX1 ALKOXYCARBONYL-5 6H-THIAZINES-1,3, INTERMEDIAIRES D'UNE NOUVELLE SYNTHESE DE CEPHEMES
5-Alkoxycarbonyl-6H-1,3-thiazines, precursors of cephems, are prepared by alkylation of 2-methylene-3, 6-dihydro-2H-1,3-thiazines or by conversion of the carbaldehyde substituted at the 5 position of a 6H-1,3-thiazine. These compounds give access to dihydrothiazinic acids converted into cephems in t...
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Veröffentlicht in: | Phosphorus and sulfur and the related elements 1987-08, Vol.32 (3-4), p.153-161 |
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container_title | Phosphorus and sulfur and the related elements |
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creator | Reliquet, A. Reliquet, F. Meslin, J. C. Sharrard, F. Quiniou, H. |
description | 5-Alkoxycarbonyl-6H-1,3-thiazines, precursors of cephems, are prepared by alkylation of 2-methylene-3, 6-dihydro-2H-1,3-thiazines or by conversion of the carbaldehyde substituted at the 5 position of a 6H-1,3-thiazine. These compounds give access to dihydrothiazinic acids converted into cephems in the presence of methanesulfonyl chloride in anhydrous chloroform.
Les alkoxycarbonyl-5 6H-thiazines-1,3 précurseurs de céphèmes sont obtenues par alkylation de méthylène-2 2H-dihydro-3,6 thiazines-1,3 ou par conversion de la fonction carbaldéhyde d'une formyl-5 thiazine. Ces composés conduisent en deux étapes aux acides dihydrothiaziniques qui sont transformés en céphèmes par le chlorure de méthanesulfonyle en milieu anhydre. |
doi_str_mv | 10.1080/03086648708074272 |
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Les alkoxycarbonyl-5 6H-thiazines-1,3 précurseurs de céphèmes sont obtenues par alkylation de méthylène-2 2H-dihydro-3,6 thiazines-1,3 ou par conversion de la fonction carbaldéhyde d'une formyl-5 thiazine. Ces composés conduisent en deux étapes aux acides dihydrothiaziniques qui sont transformés en céphèmes par le chlorure de méthanesulfonyle en milieu anhydre.</description><identifier>ISSN: 0308-664X</identifier><identifier>ISSN: 1042-6507</identifier><identifier>DOI: 10.1080/03086648708074272</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><ispartof>Phosphorus and sulfur and the related elements, 1987-08, Vol.32 (3-4), p.153-161</ispartof><rights>Copyright Taylor & Francis Group, LLC 1987</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1432-66c375b4c27ce019dce8b920ce62451668d0ab0f09529ac3b4c39b0a7d9420bf3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/03086648708074272$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/03086648708074272$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,59647,60436</link.rule.ids></links><search><creatorcontrib>Reliquet, A.</creatorcontrib><creatorcontrib>Reliquet, F.</creatorcontrib><creatorcontrib>Meslin, J. C.</creatorcontrib><creatorcontrib>Sharrard, F.</creatorcontrib><creatorcontrib>Quiniou, H.</creatorcontrib><title>ENCHAINEMENTS HETEROATOMIQUES ET LEURS PRODUITS DE CYCLISATION‒IX1 ALKOXYCARBONYL-5 6H-THIAZINES-1,3, INTERMEDIAIRES D'UNE NOUVELLE SYNTHESE DE CEPHEMES</title><title>Phosphorus and sulfur and the related elements</title><description>5-Alkoxycarbonyl-6H-1,3-thiazines, precursors of cephems, are prepared by alkylation of 2-methylene-3, 6-dihydro-2H-1,3-thiazines or by conversion of the carbaldehyde substituted at the 5 position of a 6H-1,3-thiazine. These compounds give access to dihydrothiazinic acids converted into cephems in the presence of methanesulfonyl chloride in anhydrous chloroform.
Les alkoxycarbonyl-5 6H-thiazines-1,3 précurseurs de céphèmes sont obtenues par alkylation de méthylène-2 2H-dihydro-3,6 thiazines-1,3 ou par conversion de la fonction carbaldéhyde d'une formyl-5 thiazine. Ces composés conduisent en deux étapes aux acides dihydrothiaziniques qui sont transformés en céphèmes par le chlorure de méthanesulfonyle en milieu anhydre.</description><issn>0308-664X</issn><issn>1042-6507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNp1kD1Ow0AQhV2ARBRyALrtaGLY9fpXojH2gFc4u8E_KKax7LUtBSUY2UgoHWeg5HichA2hQ0wzmqf3Ps2Mpp0RfEGwiy8xxa5tm66jBsc0HONIm-w1XYmrE202jk9YlWVTD1sT7RN4EPmMwwJ4lqIIMkiEn4kFu88hRZChGPIkRctEhDlTjhBQUAQxS_2MCf71_sFWBPnxnVgVgZ9cC17EuoXsSM8i5j8qcKqTOZ0jxhV5ASHzWaLA4XnOAXGRP0AcA0oLnkWQwg8elpFaJz3VjrtqM7az3z7V8hvIgkiPxS0L_FiXxKSGuktSx6pNaTiyxcRrZOvWnoFlaxumRWzbbXBV4w57luFVkion9WpcOY1nGrju6FQjB64c-nEc2q58GdbbatiVBJf7n5Z_fqoyV4fM-rnrh2311g-bpnytdpt-6IbqWa7Hkv4f_wYYCXMc</recordid><startdate>19870801</startdate><enddate>19870801</enddate><creator>Reliquet, A.</creator><creator>Reliquet, F.</creator><creator>Meslin, J. C.</creator><creator>Sharrard, F.</creator><creator>Quiniou, H.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19870801</creationdate><title>ENCHAINEMENTS HETEROATOMIQUES ET LEURS PRODUITS DE CYCLISATION‒IX1 ALKOXYCARBONYL-5 6H-THIAZINES-1,3, INTERMEDIAIRES D'UNE NOUVELLE SYNTHESE DE CEPHEMES</title><author>Reliquet, A. ; Reliquet, F. ; Meslin, J. C. ; Sharrard, F. ; Quiniou, H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1432-66c375b4c27ce019dce8b920ce62451668d0ab0f09529ac3b4c39b0a7d9420bf3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reliquet, A.</creatorcontrib><creatorcontrib>Reliquet, F.</creatorcontrib><creatorcontrib>Meslin, J. C.</creatorcontrib><creatorcontrib>Sharrard, F.</creatorcontrib><creatorcontrib>Quiniou, H.</creatorcontrib><collection>CrossRef</collection><jtitle>Phosphorus and sulfur and the related elements</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reliquet, A.</au><au>Reliquet, F.</au><au>Meslin, J. C.</au><au>Sharrard, F.</au><au>Quiniou, H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ENCHAINEMENTS HETEROATOMIQUES ET LEURS PRODUITS DE CYCLISATION‒IX1 ALKOXYCARBONYL-5 6H-THIAZINES-1,3, INTERMEDIAIRES D'UNE NOUVELLE SYNTHESE DE CEPHEMES</atitle><jtitle>Phosphorus and sulfur and the related elements</jtitle><date>1987-08-01</date><risdate>1987</risdate><volume>32</volume><issue>3-4</issue><spage>153</spage><epage>161</epage><pages>153-161</pages><issn>0308-664X</issn><issn>1042-6507</issn><abstract>5-Alkoxycarbonyl-6H-1,3-thiazines, precursors of cephems, are prepared by alkylation of 2-methylene-3, 6-dihydro-2H-1,3-thiazines or by conversion of the carbaldehyde substituted at the 5 position of a 6H-1,3-thiazine. These compounds give access to dihydrothiazinic acids converted into cephems in the presence of methanesulfonyl chloride in anhydrous chloroform.
Les alkoxycarbonyl-5 6H-thiazines-1,3 précurseurs de céphèmes sont obtenues par alkylation de méthylène-2 2H-dihydro-3,6 thiazines-1,3 ou par conversion de la fonction carbaldéhyde d'une formyl-5 thiazine. Ces composés conduisent en deux étapes aux acides dihydrothiaziniques qui sont transformés en céphèmes par le chlorure de méthanesulfonyle en milieu anhydre.</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/03086648708074272</doi><tpages>9</tpages></addata></record> |
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title | ENCHAINEMENTS HETEROATOMIQUES ET LEURS PRODUITS DE CYCLISATION‒IX1 ALKOXYCARBONYL-5 6H-THIAZINES-1,3, INTERMEDIAIRES D'UNE NOUVELLE SYNTHESE DE CEPHEMES |
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