Total Synthesis of CyrneineA

Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a sy...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Angewandte Chemie International Edition 2012-04, Vol.51 (17), p.4071-4073
Hauptverfasser: Elamparuthi, Elangovan, Fellay, Cindy, Neuburger, Markus, Gademann, Karl
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 4073
container_issue 17
container_start_page 4071
container_title Angewandte Chemie International Edition
container_volume 51
creator Elamparuthi, Elangovan
Fellay, Cindy
Neuburger, Markus
Gademann, Karl
description Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample.
doi_str_mv 10.1002/anie.201200515
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_1701076627</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2944417331</sourcerecordid><originalsourceid>FETCH-LOGICAL-p617-fb511f46003af0124ce24d745304dca01731bc97d6ed49a0a7ff0fa94010258a3</originalsourceid><addsrcrecordid>eNpdjztPwzAUhS0EEqWwMjFEYmFJudfX9k3GKuIlVWIge-QmtkgVnBInQ_89lmBiOmf4dB5C3CJsEEA-2tC7jQSUABr1mVihlpgTM50nr4hyLjReiqsYD4kvCjArcVePsx2yj1OYP13sYzb6rDpNwfXBba_FhbdDdDd_uhb181Ndvea795e3arvLjwY593uN6JUBIOtTvWqdVB0rTaC61gIy4b4tuTOuU6UFy96Dt6UCBKkLS2vx8Bt7nMbvxcW5-epj64bBBjcusUFOJBsjOaH3_9DDuEwhjWuQpGFKv5B-AHRdSpI</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1326730281</pqid></control><display><type>article</type><title>Total Synthesis of CyrneineA</title><source>Wiley Online Library</source><creator>Elamparuthi, Elangovan ; Fellay, Cindy ; Neuburger, Markus ; Gademann, Karl</creator><creatorcontrib>Elamparuthi, Elangovan ; Fellay, Cindy ; Neuburger, Markus ; Gademann, Karl</creatorcontrib><description>Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample.</description><edition>International ed. in English</edition><identifier>ISSN: 1433-7851</identifier><identifier>EISSN: 1521-3773</identifier><identifier>DOI: 10.1002/anie.201200515</identifier><identifier>CODEN: ACIEAY</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>Carbenes ; Carbonyls ; Crystal structure ; Natural products ; Synthesis ; X-rays</subject><ispartof>Angewandte Chemie International Edition, 2012-04, Vol.51 (17), p.4071-4073</ispartof><rights>Copyright © 2012 WILEY-VCH Verlag GmbH &amp; Co. KGaA, Weinheim</rights><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>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Elamparuthi, Elangovan</creatorcontrib><creatorcontrib>Fellay, Cindy</creatorcontrib><creatorcontrib>Neuburger, Markus</creatorcontrib><creatorcontrib>Gademann, Karl</creatorcontrib><title>Total Synthesis of CyrneineA</title><title>Angewandte Chemie International Edition</title><description>Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample.</description><subject>Carbenes</subject><subject>Carbonyls</subject><subject>Crystal structure</subject><subject>Natural products</subject><subject>Synthesis</subject><subject>X-rays</subject><issn>1433-7851</issn><issn>1521-3773</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNpdjztPwzAUhS0EEqWwMjFEYmFJudfX9k3GKuIlVWIge-QmtkgVnBInQ_89lmBiOmf4dB5C3CJsEEA-2tC7jQSUABr1mVihlpgTM50nr4hyLjReiqsYD4kvCjArcVePsx2yj1OYP13sYzb6rDpNwfXBba_FhbdDdDd_uhb181Ndvea795e3arvLjwY593uN6JUBIOtTvWqdVB0rTaC61gIy4b4tuTOuU6UFy96Dt6UCBKkLS2vx8Bt7nMbvxcW5-epj64bBBjcusUFOJBsjOaH3_9DDuEwhjWuQpGFKv5B-AHRdSpI</recordid><startdate>20120423</startdate><enddate>20120423</enddate><creator>Elamparuthi, Elangovan</creator><creator>Fellay, Cindy</creator><creator>Neuburger, Markus</creator><creator>Gademann, Karl</creator><general>Wiley Subscription Services, Inc</general><scope>7TM</scope><scope>K9.</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20120423</creationdate><title>Total Synthesis of CyrneineA</title><author>Elamparuthi, Elangovan ; Fellay, Cindy ; Neuburger, Markus ; Gademann, Karl</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p617-fb511f46003af0124ce24d745304dca01731bc97d6ed49a0a7ff0fa94010258a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Carbenes</topic><topic>Carbonyls</topic><topic>Crystal structure</topic><topic>Natural products</topic><topic>Synthesis</topic><topic>X-rays</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Elamparuthi, Elangovan</creatorcontrib><creatorcontrib>Fellay, Cindy</creatorcontrib><creatorcontrib>Neuburger, Markus</creatorcontrib><creatorcontrib>Gademann, Karl</creatorcontrib><collection>Nucleic Acids Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Angewandte Chemie International Edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Elamparuthi, Elangovan</au><au>Fellay, Cindy</au><au>Neuburger, Markus</au><au>Gademann, Karl</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Total Synthesis of CyrneineA</atitle><jtitle>Angewandte Chemie International Edition</jtitle><date>2012-04-23</date><risdate>2012</risdate><volume>51</volume><issue>17</issue><spage>4071</spage><epage>4073</epage><pages>4071-4073</pages><issn>1433-7851</issn><eissn>1521-3773</eissn><coden>ACIEAY</coden><abstract>Neuritogenic natural products: The tricyclic diterpene cyrneineA featuring a hexatrienal unit was prepared synthetically for the first time by a Heck reaction, a carbene ring expansion, and a reductive carbonylation. The structure of the natural product was assigned by X-ray crystal analysis of a synthetic sample.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/anie.201200515</doi><tpages>3</tpages><edition>International ed. in English</edition></addata></record>
fulltext fulltext
identifier ISSN: 1433-7851
ispartof Angewandte Chemie International Edition, 2012-04, Vol.51 (17), p.4071-4073
issn 1433-7851
1521-3773
language eng
recordid cdi_proquest_miscellaneous_1701076627
source Wiley Online Library
subjects Carbenes
Carbonyls
Crystal structure
Natural products
Synthesis
X-rays
title Total Synthesis of CyrneineA
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-03T17%3A13%3A40IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Total%20Synthesis%20of%20CyrneineA&rft.jtitle=Angewandte%20Chemie%20International%20Edition&rft.au=Elamparuthi,%20Elangovan&rft.date=2012-04-23&rft.volume=51&rft.issue=17&rft.spage=4071&rft.epage=4073&rft.pages=4071-4073&rft.issn=1433-7851&rft.eissn=1521-3773&rft.coden=ACIEAY&rft_id=info:doi/10.1002/anie.201200515&rft_dat=%3Cproquest%3E2944417331%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1326730281&rft_id=info:pmid/&rfr_iscdi=true