Syntheses of 3',4',5,6-tetradioxyneamine and 5,6-dideoxyneamine
3',4',5,6-Tetradoxyneamine (7) was synthesized from neamine by the reaction sequence N-acetylation, O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hyrolysis, Alternatively, 7 was obtained by treatment of tetra-(N-methoxycarbonyl)neamine with sulphuryl chlorid...
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Veröffentlicht in: | Carbohydrate research 1977-10, Vol.58 (2), p.379-385 |
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description | 3',4',5,6-Tetradoxyneamine (7) was synthesized from neamine by the reaction sequence N-acetylation, O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hyrolysis, Alternatively, 7 was obtained by treatment of tetra-(N-methoxycarbonyl)neamine with sulphuryl chloride, followed by hydrogenation in the presence of palladium-on-charcoal and triethylamine, and removal of the N-protecting groups. 5,6-Dideoxyneamine (11) was synthesized from known 5,6-O-cyclohexylidene-tetra-(N-methoxycarbonyl)neamine by the reaction sequence 3',4'-O-acetylation, removal of the 5,6-O-cyclohexylidene group, 5,6-di-O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hydrolysis. An alternative route involved treatment of 3',4'-di-O-acetyl-tetra-(N-methoxycarbonyl)-neamine (8) with sulphuryl chloride, hydrogenation of the product, and removal of the protecting groups to give 11. |
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An alternative route involved treatment of 3',4'-di-O-acetyl-tetra-(N-methoxycarbonyl)-neamine (8) with sulphuryl chloride, hydrogenation of the product, and removal of the protecting groups to give 11.</description><identifier>ISSN: 0008-6215</identifier><identifier>PMID: 912693</identifier><language>eng</language><publisher>Netherlands</publisher><subject>Magnetic Resonance Spectroscopy ; Methods ; Neomycin - analogs & derivatives ; Neomycin - chemical synthesis ; Optical Rotation ; Structure-Activity Relationship</subject><ispartof>Carbohydrate research, 1977-10, Vol.58 (2), p.379-385</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/912693$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Canas-Rodriguez, A</creatorcontrib><creatorcontrib>Ruiz-Poveda, S G</creatorcontrib><title>Syntheses of 3',4',5,6-tetradioxyneamine and 5,6-dideoxyneamine</title><title>Carbohydrate research</title><addtitle>Carbohydr Res</addtitle><description>3',4',5,6-Tetradoxyneamine (7) was synthesized from neamine by the reaction sequence N-acetylation, O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hyrolysis, Alternatively, 7 was obtained by treatment of tetra-(N-methoxycarbonyl)neamine with sulphuryl chloride, followed by hydrogenation in the presence of palladium-on-charcoal and triethylamine, and removal of the N-protecting groups. 5,6-Dideoxyneamine (11) was synthesized from known 5,6-O-cyclohexylidene-tetra-(N-methoxycarbonyl)neamine by the reaction sequence 3',4'-O-acetylation, removal of the 5,6-O-cyclohexylidene group, 5,6-di-O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hydrolysis. An alternative route involved treatment of 3',4'-di-O-acetyl-tetra-(N-methoxycarbonyl)-neamine (8) with sulphuryl chloride, hydrogenation of the product, and removal of the protecting groups to give 11.</description><subject>Magnetic Resonance Spectroscopy</subject><subject>Methods</subject><subject>Neomycin - analogs & derivatives</subject><subject>Neomycin - chemical synthesis</subject><subject>Optical Rotation</subject><subject>Structure-Activity Relationship</subject><issn>0008-6215</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1977</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFj0trwzAQhHXoK037D3rwqbnEYGktyXsqJfQFgR6au1lLa-riVy0b6n9flwR6GmbmY2DOxCpJkiw2SuorcR3C12ITY82luECpDMJKPHzM7fjJgUPUlRFstulmq7cmHnkcyFfdz9wyNVXLEbU--mt85fk_vhHnJdWBb0-6Fofnp8PuNd6_v7ztHvdxrxXEAJmjDK31xJbIKixdgkqiB4mYSmvYZErTwhaoHYEsyDqQVhKDQw1rcX-c7Yfue-Iw5k0VHNc1tdxNIbdgMJNpuoB3J3AqGvZ5P1QNDXN-_Au_8z1Nkg</recordid><startdate>197710</startdate><enddate>197710</enddate><creator>Canas-Rodriguez, A</creator><creator>Ruiz-Poveda, S G</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>197710</creationdate><title>Syntheses of 3',4',5,6-tetradioxyneamine and 5,6-dideoxyneamine</title><author>Canas-Rodriguez, A ; Ruiz-Poveda, S G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p523-338ca8977dae7aa729fc09219d31994176e6825a523b95ca31ba7c3171ae3c953</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1977</creationdate><topic>Magnetic Resonance Spectroscopy</topic><topic>Methods</topic><topic>Neomycin - analogs & derivatives</topic><topic>Neomycin - chemical synthesis</topic><topic>Optical Rotation</topic><topic>Structure-Activity Relationship</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Canas-Rodriguez, A</creatorcontrib><creatorcontrib>Ruiz-Poveda, S G</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Carbohydrate research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Canas-Rodriguez, A</au><au>Ruiz-Poveda, S G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Syntheses of 3',4',5,6-tetradioxyneamine and 5,6-dideoxyneamine</atitle><jtitle>Carbohydrate research</jtitle><addtitle>Carbohydr Res</addtitle><date>1977-10</date><risdate>1977</risdate><volume>58</volume><issue>2</issue><spage>379</spage><epage>385</epage><pages>379-385</pages><issn>0008-6215</issn><abstract>3',4',5,6-Tetradoxyneamine (7) was synthesized from neamine by the reaction sequence N-acetylation, O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hyrolysis, Alternatively, 7 was obtained by treatment of tetra-(N-methoxycarbonyl)neamine with sulphuryl chloride, followed by hydrogenation in the presence of palladium-on-charcoal and triethylamine, and removal of the N-protecting groups. 5,6-Dideoxyneamine (11) was synthesized from known 5,6-O-cyclohexylidene-tetra-(N-methoxycarbonyl)neamine by the reaction sequence 3',4'-O-acetylation, removal of the 5,6-O-cyclohexylidene group, 5,6-di-O-mesylation, treatment with sodium iodide-zinc dust, hydrogenation, and base hydrolysis. An alternative route involved treatment of 3',4'-di-O-acetyl-tetra-(N-methoxycarbonyl)-neamine (8) with sulphuryl chloride, hydrogenation of the product, and removal of the protecting groups to give 11.</abstract><cop>Netherlands</cop><pmid>912693</pmid><tpages>7</tpages></addata></record> |
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subjects | Magnetic Resonance Spectroscopy Methods Neomycin - analogs & derivatives Neomycin - chemical synthesis Optical Rotation Structure-Activity Relationship |
title | Syntheses of 3',4',5,6-tetradioxyneamine and 5,6-dideoxyneamine |
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