Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool

Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool

An efficient method for the synthesis of (+)-coronarin E 1, (+)- epi-coronarin A 2 and (+)-15, 16-epoxy-8(17), 13(16), 14-labdatriene 3 via the homodrimane 9, obtained in four steps from (+)-manool 5, is described.

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of chemical research 2003-08, Vol.2003 (8), p.504-506
Hauptverfasser: Villamizar, José, Salazar, Franklin, Fuentes, Juan, Tropper, Eleonora, Alonso, Randolph
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 506
container_issue 8
container_start_page 504
container_title Journal of chemical research
container_volume 2003
creator Villamizar, José
Salazar, Franklin
Fuentes, Juan
Tropper, Eleonora
Alonso, Randolph
description An efficient method for the synthesis of (+)-coronarin E 1, (+)- epi-coronarin A 2 and (+)-15, 16-epoxy-8(17), 13(16), 14-labdatriene 3 via the homodrimane 9, obtained in four steps from (+)-manool 5, is described.
doi_str_mv 10.3184/030823403103174722
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_journals_1241920935</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2847435351</sourcerecordid><originalsourceid>FETCH-LOGICAL-c273t-d4a4c482645069341ad2ce98ce64118a558744ee6d90a35b5a91e96585ebee3</originalsourceid><addsrcrecordid>eNplkE1LAzEQhoMoWKt_wFPAyxYbzeQ7RynrB1Q81PuS7mZxS7tZky20_95t60EQBl5m5pl34EXoFugDByMeKaeGcUE5DKWFZuwMjRgVmihJ9TkaHYZEgjWX6CqlFaVCKgsjtFvs2_7LpybhUOPsfkJmIYbWxabF-RRnZEI0wb5r8J-Fw66tjjDIKQZF8i7s9sRkoCdDzzNQBxVk7paV62PjW4_rGDbHm3fXhrC-Rhe1Wyd_86tjtHjOP2evZP7x8jZ7mpOSad6TSjhRCsOUkFRZLsBVrPTWlF4JAOOkNFoI71VlqeNyKZ0Fb5U00i-952N0d3LtYvje-tQXq7CN7fCwACbAMmq5HCh2osoYUoq-LrrYbFzcF0CLQ77F_3z5Dy20ZGs</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1241920935</pqid></control><display><type>article</type><title>Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool</title><source>Sage Journals GOLD Open Access 2024</source><creator>Villamizar, José ; Salazar, Franklin ; Fuentes, Juan ; Tropper, Eleonora ; Alonso, Randolph</creator><creatorcontrib>Villamizar, José ; Salazar, Franklin ; Fuentes, Juan ; Tropper, Eleonora ; Alonso, Randolph</creatorcontrib><description>An efficient method for the synthesis of (+)-coronarin E 1, (+)- epi-coronarin A 2 and (+)-15, 16-epoxy-8(17), 13(16), 14-labdatriene 3 via the homodrimane 9, obtained in four steps from (+)-manool 5, is described.</description><identifier>ISSN: 1747-5198</identifier><identifier>EISSN: 2047-6507</identifier><identifier>DOI: 10.3184/030823403103174722</identifier><language>eng</language><publisher>London: Sage Publications Ltd</publisher><ispartof>Journal of chemical research, 2003-08, Vol.2003 (8), p.504-506</ispartof><rights>Copyright Science Reviews 2000 Ltd Aug 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c273t-d4a4c482645069341ad2ce98ce64118a558744ee6d90a35b5a91e96585ebee3</citedby><cites>FETCH-LOGICAL-c273t-d4a4c482645069341ad2ce98ce64118a558744ee6d90a35b5a91e96585ebee3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Villamizar, José</creatorcontrib><creatorcontrib>Salazar, Franklin</creatorcontrib><creatorcontrib>Fuentes, Juan</creatorcontrib><creatorcontrib>Tropper, Eleonora</creatorcontrib><creatorcontrib>Alonso, Randolph</creatorcontrib><title>Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool</title><title>Journal of chemical research</title><description>An efficient method for the synthesis of (+)-coronarin E 1, (+)- epi-coronarin A 2 and (+)-15, 16-epoxy-8(17), 13(16), 14-labdatriene 3 via the homodrimane 9, obtained in four steps from (+)-manool 5, is described.</description><issn>1747-5198</issn><issn>2047-6507</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNplkE1LAzEQhoMoWKt_wFPAyxYbzeQ7RynrB1Q81PuS7mZxS7tZky20_95t60EQBl5m5pl34EXoFugDByMeKaeGcUE5DKWFZuwMjRgVmihJ9TkaHYZEgjWX6CqlFaVCKgsjtFvs2_7LpybhUOPsfkJmIYbWxabF-RRnZEI0wb5r8J-Fw66tjjDIKQZF8i7s9sRkoCdDzzNQBxVk7paV62PjW4_rGDbHm3fXhrC-Rhe1Wyd_86tjtHjOP2evZP7x8jZ7mpOSad6TSjhRCsOUkFRZLsBVrPTWlF4JAOOkNFoI71VlqeNyKZ0Fb5U00i-952N0d3LtYvje-tQXq7CN7fCwACbAMmq5HCh2osoYUoq-LrrYbFzcF0CLQ77F_3z5Dy20ZGs</recordid><startdate>20030801</startdate><enddate>20030801</enddate><creator>Villamizar, José</creator><creator>Salazar, Franklin</creator><creator>Fuentes, Juan</creator><creator>Tropper, Eleonora</creator><creator>Alonso, Randolph</creator><general>Sage Publications Ltd</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>CCPQU</scope><scope>D1I</scope><scope>DWQXO</scope><scope>EHMNL</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>KB.</scope><scope>PDBOC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope></search><sort><creationdate>20030801</creationdate><title>Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool</title><author>Villamizar, José ; Salazar, Franklin ; Fuentes, Juan ; Tropper, Eleonora ; Alonso, Randolph</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c273t-d4a4c482645069341ad2ce98ce64118a558744ee6d90a35b5a91e96585ebee3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Villamizar, José</creatorcontrib><creatorcontrib>Salazar, Franklin</creatorcontrib><creatorcontrib>Fuentes, Juan</creatorcontrib><creatorcontrib>Tropper, Eleonora</creatorcontrib><creatorcontrib>Alonso, Randolph</creatorcontrib><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>Materials Science &amp; Engineering Collection</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>Technology Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Materials Science Collection</collection><collection>ProQuest Central Korea</collection><collection>UK &amp; Ireland Database</collection><collection>SciTech Premium Collection</collection><collection>Materials Research Database</collection><collection>Materials Science Database</collection><collection>Materials Science Collection</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><jtitle>Journal of chemical research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Villamizar, José</au><au>Salazar, Franklin</au><au>Fuentes, Juan</au><au>Tropper, Eleonora</au><au>Alonso, Randolph</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool</atitle><jtitle>Journal of chemical research</jtitle><date>2003-08-01</date><risdate>2003</risdate><volume>2003</volume><issue>8</issue><spage>504</spage><epage>506</epage><pages>504-506</pages><issn>1747-5198</issn><eissn>2047-6507</eissn><abstract>An efficient method for the synthesis of (+)-coronarin E 1, (+)- epi-coronarin A 2 and (+)-15, 16-epoxy-8(17), 13(16), 14-labdatriene 3 via the homodrimane 9, obtained in four steps from (+)-manool 5, is described.</abstract><cop>London</cop><pub>Sage Publications Ltd</pub><doi>10.3184/030823403103174722</doi><tpages>3</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1747-5198
ispartof Journal of chemical research, 2003-08, Vol.2003 (8), p.504-506
issn 1747-5198
2047-6507
language eng
recordid cdi_proquest_journals_1241920935
source Sage Journals GOLD Open Access 2024
title Synthesis of (+)-Coronarin E, (-)-7- epi -Coronarin a and (+)-15, 16-Epoxy-8(17), 13(16), 14-Labdatriene from (+)-Manool
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-30T11%3A35%3A23IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Synthesis%20of%20(+)-Coronarin%20E,%20(-)-7-%20epi%20-Coronarin%20a%20and%20(+)-15,%2016-Epoxy-8(17),%2013(16),%2014-Labdatriene%20from%20(+)-Manool&rft.jtitle=Journal%20of%20chemical%20research&rft.au=Villamizar,%20Jos%C3%A9&rft.date=2003-08-01&rft.volume=2003&rft.issue=8&rft.spage=504&rft.epage=506&rft.pages=504-506&rft.issn=1747-5198&rft.eissn=2047-6507&rft_id=info:doi/10.3184/030823403103174722&rft_dat=%3Cproquest_cross%3E2847435351%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1241920935&rft_id=info:pmid/&rfr_iscdi=true