Relative stereochemistries of the ether rings and sugar moieties in durinskiol A
Durinskiol A ( 1) is a long carbon-chain polyol compound with a molecular weight of 2128 mu isolated from the symbiotic dinoflagellate Durinskia sp. The relative stereochemistries of ether rings and sugar moieties in 1 were established based on 2D-NMR analysis and molecular modeling studies. Conform...
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Veröffentlicht in: | Tetrahedron letters 2007-05, Vol.48 (19), p.3429-3432 |
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container_title | Tetrahedron letters |
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creator | Kita, Masaki Roy, Michael C. Siwu, Eric R.O. Noma, Isao Takiguchi, Takahiro Yamada, Kaoru Koyama, Tomoyuki Iwashita, Takeshi Wakamiya, Atsushi Uemura, Daisuke |
description | Durinskiol A (
1) is a long carbon-chain polyol compound with a molecular weight of 2128
mu isolated from the symbiotic dinoflagellate
Durinskia sp. The relative stereochemistries of ether rings and sugar moieties in
1 were established based on 2D-NMR analysis and molecular modeling studies. Conformational analysis of the 6,5,6-bis-spiroacetal ring in
1 was also examined by using ab initio methods. |
doi_str_mv | 10.1016/j.tetlet.2007.03.039 |
format | Article |
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1) is a long carbon-chain polyol compound with a molecular weight of 2128
mu isolated from the symbiotic dinoflagellate
Durinskia sp. The relative stereochemistries of ether rings and sugar moieties in
1 were established based on 2D-NMR analysis and molecular modeling studies. Conformational analysis of the 6,5,6-bis-spiroacetal ring in
1 was also examined by using ab initio methods.</description><identifier>ISSN: 0040-4039</identifier><identifier>EISSN: 1873-3581</identifier><identifier>DOI: 10.1016/j.tetlet.2007.03.039</identifier><language>eng</language><publisher>Elsevier Ltd</publisher><subject>Configuration determination ; Durinskia ; Glycosides ; Molecular modeling ; Natural products ; Super-carbon-chain compounds</subject><ispartof>Tetrahedron letters, 2007-05, Vol.48 (19), p.3429-3432</ispartof><rights>2007 Elsevier Ltd</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c403t-578f5891014e10bcf4c88d4e66e2f8d2789db484b190cf34708206b95d74dff13</citedby><cites>FETCH-LOGICAL-c403t-578f5891014e10bcf4c88d4e66e2f8d2789db484b190cf34708206b95d74dff13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.tetlet.2007.03.039$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids></links><search><creatorcontrib>Kita, Masaki</creatorcontrib><creatorcontrib>Roy, Michael C.</creatorcontrib><creatorcontrib>Siwu, Eric R.O.</creatorcontrib><creatorcontrib>Noma, Isao</creatorcontrib><creatorcontrib>Takiguchi, Takahiro</creatorcontrib><creatorcontrib>Yamada, Kaoru</creatorcontrib><creatorcontrib>Koyama, Tomoyuki</creatorcontrib><creatorcontrib>Iwashita, Takeshi</creatorcontrib><creatorcontrib>Wakamiya, Atsushi</creatorcontrib><creatorcontrib>Uemura, Daisuke</creatorcontrib><title>Relative stereochemistries of the ether rings and sugar moieties in durinskiol A</title><title>Tetrahedron letters</title><description>Durinskiol A (
1) is a long carbon-chain polyol compound with a molecular weight of 2128
mu isolated from the symbiotic dinoflagellate
Durinskia sp. The relative stereochemistries of ether rings and sugar moieties in
1 were established based on 2D-NMR analysis and molecular modeling studies. Conformational analysis of the 6,5,6-bis-spiroacetal ring in
1 was also examined by using ab initio methods.</description><subject>Configuration determination</subject><subject>Durinskia</subject><subject>Glycosides</subject><subject>Molecular modeling</subject><subject>Natural products</subject><subject>Super-carbon-chain compounds</subject><issn>0040-4039</issn><issn>1873-3581</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp9UE1LxDAQDaLguvoPPOTkreukTdv0IiyLX7CgiJ5Dm0x2s3YbTdIF_71Z6tlhmIGZ94Y3j5BrBgsGrLrdLSLGHuMiB6gXUKRsTsiMibrIilKwUzID4JDxND8nFyHsIEUlYEZe37Bvoz0gDRE9OrXFvQ3RWwzUGRq3SDEVT70dNoG2g6Zh3LSe7p3FeETZgeoxbcOndT1dXpIz0_YBr_76nHw83L-vnrL1y-PzarnOVFIRs7IWphRNks-RQacMV0JojlWFuRE6r0WjOy54xxpQpuA1iByqril1zbUxrJiTm-nul3ffI4Yok26Ffd8O6MYgc5bzMj2fgHwCKu9C8Gjkl7f71v9IBvJon9zJyT55tE9CkbJJtLuJhumJg0Uvg7I4KNTWo4pSO_v_gV_plHs4</recordid><startdate>20070501</startdate><enddate>20070501</enddate><creator>Kita, Masaki</creator><creator>Roy, Michael C.</creator><creator>Siwu, Eric R.O.</creator><creator>Noma, Isao</creator><creator>Takiguchi, Takahiro</creator><creator>Yamada, Kaoru</creator><creator>Koyama, Tomoyuki</creator><creator>Iwashita, Takeshi</creator><creator>Wakamiya, Atsushi</creator><creator>Uemura, Daisuke</creator><general>Elsevier Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>M7N</scope></search><sort><creationdate>20070501</creationdate><title>Relative stereochemistries of the ether rings and sugar moieties in durinskiol A</title><author>Kita, Masaki ; Roy, Michael C. ; Siwu, Eric R.O. ; Noma, Isao ; Takiguchi, Takahiro ; Yamada, Kaoru ; Koyama, Tomoyuki ; Iwashita, Takeshi ; Wakamiya, Atsushi ; Uemura, Daisuke</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c403t-578f5891014e10bcf4c88d4e66e2f8d2789db484b190cf34708206b95d74dff13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Configuration determination</topic><topic>Durinskia</topic><topic>Glycosides</topic><topic>Molecular modeling</topic><topic>Natural products</topic><topic>Super-carbon-chain compounds</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kita, Masaki</creatorcontrib><creatorcontrib>Roy, Michael C.</creatorcontrib><creatorcontrib>Siwu, Eric R.O.</creatorcontrib><creatorcontrib>Noma, Isao</creatorcontrib><creatorcontrib>Takiguchi, Takahiro</creatorcontrib><creatorcontrib>Yamada, Kaoru</creatorcontrib><creatorcontrib>Koyama, Tomoyuki</creatorcontrib><creatorcontrib>Iwashita, Takeshi</creatorcontrib><creatorcontrib>Wakamiya, Atsushi</creatorcontrib><creatorcontrib>Uemura, Daisuke</creatorcontrib><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Tetrahedron letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kita, Masaki</au><au>Roy, Michael C.</au><au>Siwu, Eric R.O.</au><au>Noma, Isao</au><au>Takiguchi, Takahiro</au><au>Yamada, Kaoru</au><au>Koyama, Tomoyuki</au><au>Iwashita, Takeshi</au><au>Wakamiya, Atsushi</au><au>Uemura, Daisuke</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Relative stereochemistries of the ether rings and sugar moieties in durinskiol A</atitle><jtitle>Tetrahedron letters</jtitle><date>2007-05-01</date><risdate>2007</risdate><volume>48</volume><issue>19</issue><spage>3429</spage><epage>3432</epage><pages>3429-3432</pages><issn>0040-4039</issn><eissn>1873-3581</eissn><abstract>Durinskiol A (
1) is a long carbon-chain polyol compound with a molecular weight of 2128
mu isolated from the symbiotic dinoflagellate
Durinskia sp. The relative stereochemistries of ether rings and sugar moieties in
1 were established based on 2D-NMR analysis and molecular modeling studies. Conformational analysis of the 6,5,6-bis-spiroacetal ring in
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language | eng |
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source | Elsevier ScienceDirect Journals Complete |
subjects | Configuration determination Durinskia Glycosides Molecular modeling Natural products Super-carbon-chain compounds |
title | Relative stereochemistries of the ether rings and sugar moieties in durinskiol A |
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