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Total Synthesis of 4′′-O-Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment
A disaccharide compound, p‐methoxyphenyl 2,3,4‐tri‐O‐benzyl‐β‐L‐arabinopyranosyl‐(1→6)‐2‐O‐benzyl‐3,4‐di‐O‐acetyl‐β‐D‐galactopyranoside (17), was successfully synthesized from two monosaccharides L‐arabinose and D‐galactose and fully characterized. This compound can be used to build a natural produc...
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Published in: | Chinese journal of chemistry 2008-01, Vol.26 (1), p.158-164 |
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container_start_page | 158 |
container_title | Chinese journal of chemistry |
container_volume | 26 |
creator | ZHAO, Gui-Long YU, Zhao-Yun LI, Yan PANG, Li-Na WANG, Jian-Wu |
description | A disaccharide compound, p‐methoxyphenyl 2,3,4‐tri‐O‐benzyl‐β‐L‐arabinopyranosyl‐(1→6)‐2‐O‐benzyl‐3,4‐di‐O‐acetyl‐β‐D‐galactopyranoside (17), was successfully synthesized from two monosaccharides L‐arabinose and D‐galactose and fully characterized. This compound can be used to build a natural product 4″‐O‐acetylmanan thoside B, which was isolated from the leaves and stems of a kind of Vietnamese Acanthaceae Justicia patentiflora. |
doi_str_mv | 10.1002/cjoc.200890014 |
format | article |
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This compound can be used to build a natural product 4″‐O‐acetylmanan thoside B, which was isolated from the leaves and stems of a kind of Vietnamese Acanthaceae Justicia patentiflora.</description><identifier>ISSN: 1001-604X</identifier><identifier>EISSN: 1614-7065</identifier><identifier>DOI: 10.1002/cjoc.200890014</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>4′′-O-acetylmananthoside B ; arabinose ; galactose ; saccharide ; total synthesis ; total synthesis, arabinose</subject><ispartof>Chinese journal of chemistry, 2008-01, Vol.26 (1), p.158-164</ispartof><rights>Copyright © 2008 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3274-c5eba2bfd2ea5b8dcd4c760f943a45ee7c73454923caa86c1eeb7d012c1468423</citedby><cites>FETCH-LOGICAL-c3274-c5eba2bfd2ea5b8dcd4c760f943a45ee7c73454923caa86c1eeb7d012c1468423</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27922,27923</link.rule.ids></links><search><creatorcontrib>ZHAO, Gui-Long</creatorcontrib><creatorcontrib>YU, Zhao-Yun</creatorcontrib><creatorcontrib>LI, Yan</creatorcontrib><creatorcontrib>PANG, Li-Na</creatorcontrib><creatorcontrib>WANG, Jian-Wu</creatorcontrib><title>Total Synthesis of 4′′-O-Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment</title><title>Chinese journal of chemistry</title><addtitle>Chin. J. Chem</addtitle><description>A disaccharide compound, p‐methoxyphenyl 2,3,4‐tri‐O‐benzyl‐β‐L‐arabinopyranosyl‐(1→6)‐2‐O‐benzyl‐3,4‐di‐O‐acetyl‐β‐D‐galactopyranoside (17), was successfully synthesized from two monosaccharides L‐arabinose and D‐galactose and fully characterized. This compound can be used to build a natural product 4″‐O‐acetylmanan thoside B, which was isolated from the leaves and stems of a kind of Vietnamese Acanthaceae Justicia patentiflora.</description><subject>4′′-O-acetylmananthoside B</subject><subject>arabinose</subject><subject>galactose</subject><subject>saccharide</subject><subject>total synthesis</subject><subject>total synthesis, arabinose</subject><issn>1001-604X</issn><issn>1614-7065</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><recordid>eNqFkEFOwzAQRS0EEqWwZZ0LuNiOYyfs2pSWoIoiUVrExpo4Dk1JG2RHguw4E0fiJKQqqmCFNNJ8zfz3Fx-hc0p6lBB2oVeV7jFCwogQyg9QhwrKsSQiOGx1e8OC8MdjdOLcqvVLyUQHwayqofTum029NK5wXpV7_Ovjsx08xX1t6qZcwwbad-WKzHgD7w5s7SXJ5V-oVd6wcKD1EuzWOLLwvDab-hQd5VA6c_azu-hhdDWLr_FkOk7i_gRrn0mOdWBSYGmeMQNBGmY641oKkkfcBx4YI7X0ecAj5muAUGhqTCozQpmmXISc-V3U2-VqWzlnTa5ebbEG2yhK1LYgtS1I7QtqgWgHvBWlaf5xq_hmGv9m8Y4tXG3e9yzYFyWkLwO1uB2rQfS0kGQ4V3P_G83we_4</recordid><startdate>200801</startdate><enddate>200801</enddate><creator>ZHAO, Gui-Long</creator><creator>YU, Zhao-Yun</creator><creator>LI, Yan</creator><creator>PANG, Li-Na</creator><creator>WANG, Jian-Wu</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200801</creationdate><title>Total Synthesis of 4′′-O-Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment</title><author>ZHAO, Gui-Long ; YU, Zhao-Yun ; LI, Yan ; PANG, Li-Na ; WANG, Jian-Wu</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3274-c5eba2bfd2ea5b8dcd4c760f943a45ee7c73454923caa86c1eeb7d012c1468423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>4′′-O-acetylmananthoside B</topic><topic>arabinose</topic><topic>galactose</topic><topic>saccharide</topic><topic>total synthesis</topic><topic>total synthesis, arabinose</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ZHAO, Gui-Long</creatorcontrib><creatorcontrib>YU, Zhao-Yun</creatorcontrib><creatorcontrib>LI, Yan</creatorcontrib><creatorcontrib>PANG, Li-Na</creatorcontrib><creatorcontrib>WANG, Jian-Wu</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Chinese journal of chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ZHAO, Gui-Long</au><au>YU, Zhao-Yun</au><au>LI, Yan</au><au>PANG, Li-Na</au><au>WANG, Jian-Wu</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Total Synthesis of 4′′-O-Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment</atitle><jtitle>Chinese journal of chemistry</jtitle><addtitle>Chin. J. Chem</addtitle><date>2008-01</date><risdate>2008</risdate><volume>26</volume><issue>1</issue><spage>158</spage><epage>164</epage><pages>158-164</pages><issn>1001-604X</issn><eissn>1614-7065</eissn><abstract>A disaccharide compound, p‐methoxyphenyl 2,3,4‐tri‐O‐benzyl‐β‐L‐arabinopyranosyl‐(1→6)‐2‐O‐benzyl‐3,4‐di‐O‐acetyl‐β‐D‐galactopyranoside (17), was successfully synthesized from two monosaccharides L‐arabinose and D‐galactose and fully characterized. This compound can be used to build a natural product 4″‐O‐acetylmanan thoside B, which was isolated from the leaves and stems of a kind of Vietnamese Acanthaceae Justicia patentiflora.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/cjoc.200890014</doi><tpages>7</tpages></addata></record> |
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subjects | 4′′-O-acetylmananthoside B arabinose galactose saccharide total synthesis total synthesis, arabinose |
title | Total Synthesis of 4′′-O-Acetylmananthoside B Part II: Synthesis of the Disaccharide Fragment |
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