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Synthesis of the C19-C34 Segment of Amphidinolide C
Abstract The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski’s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.
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Published in: | Synlett 2007-03, Vol.2007 (4), p.0567-0570 |
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Language: | English |
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container_end_page | 0570 |
container_issue | 4 |
container_start_page | 0567 |
container_title | Synlett |
container_volume | 2007 |
creator | Mohapatra, Debendra K. Rahaman, Hasibur Chorghade, Mukund S. Gurjar, Mukund K. |
description | Abstract
The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski’s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction. |
doi_str_mv | 10.1055/s-2007-967968 |
format | article |
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The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski’s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2007-967968</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2007-03, Vol.2007 (4), p.0567-0570</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c274t-3b4124d89573675519c2b0db35f789dcd30114675c558c1c2e307a486df8dee03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2007-967968.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2007-967968$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,27924,27925,54559,54560</link.rule.ids></links><search><creatorcontrib>Mohapatra, Debendra K.</creatorcontrib><creatorcontrib>Rahaman, Hasibur</creatorcontrib><creatorcontrib>Chorghade, Mukund S.</creatorcontrib><creatorcontrib>Gurjar, Mukund K.</creatorcontrib><title>Synthesis of the C19-C34 Segment of Amphidinolide C</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski’s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNp1j01LxDAQhoMoWFeP3vsDjE6-k-NS_IIFD6vn0CapzbJtl6Ye9t-bUq-eZnjfh2EehO4JPBIQ4ilhCqCwkcpIfYEKwpnKkZGXqADDJBaU8Gt0k9IBgHBtoEBsfx7mLqSYyrEt81ZWxOCK8XIfvvswzEu87U9d9HEYj9Fn4BZdtfUxhbu_uUFfL8-f1Rvefby-V9sddlTxGbOGE8q9NkIxqYQgxtEGfMNEq7TxzjMghOfGCaEdcTQwUDXX0rfahwBsg_B6101jSlNo7WmKfT2dLQG7GNtkF2O7Gmf-YeXnLoY-2MP4Mw35wX_wX3Q-U8w</recordid><startdate>20070301</startdate><enddate>20070301</enddate><creator>Mohapatra, Debendra K.</creator><creator>Rahaman, Hasibur</creator><creator>Chorghade, Mukund S.</creator><creator>Gurjar, Mukund K.</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20070301</creationdate><title>Synthesis of the C19-C34 Segment of Amphidinolide C</title><author>Mohapatra, Debendra K. ; Rahaman, Hasibur ; Chorghade, Mukund S. ; Gurjar, Mukund K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c274t-3b4124d89573675519c2b0db35f789dcd30114675c558c1c2e307a486df8dee03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mohapatra, Debendra K.</creatorcontrib><creatorcontrib>Rahaman, Hasibur</creatorcontrib><creatorcontrib>Chorghade, Mukund S.</creatorcontrib><creatorcontrib>Gurjar, Mukund K.</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mohapatra, Debendra K.</au><au>Rahaman, Hasibur</au><au>Chorghade, Mukund S.</au><au>Gurjar, Mukund K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of the C19-C34 Segment of Amphidinolide C</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2007-03-01</date><risdate>2007</risdate><volume>2007</volume><issue>4</issue><spage>0567</spage><epage>0570</epage><pages>0567-0570</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
The synthesis of the C19-C34 segment of amphidinolide C is described. The key steps include the Mioskowski’s Lewis acid catalyzed epoxide opening with the alcohol, ring-closing metathesis, Wittig reaction, and Nozaki-Hiyama-Kishi coupling reaction.</abstract><doi>10.1055/s-2007-967968</doi><tpages>4</tpages></addata></record> |
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source | Thieme Connect Journals |
subjects | letter |
title | Synthesis of the C19-C34 Segment of Amphidinolide C |
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