Sythese von α und β‐Sinensal

Sythese von α und β‐Sinensal

β‐Sinensal (2,6‐dimethyl‐10‐methylene‐dodeca‐2,6,11‐trienal) was synthesized from the diene‐aldehyde 5. This was converted into the trans‐ and cis‐triene‐aldehydes 16 and 17, which were condensed with the phosphorane 18 to give the corresponding two geometrical isomers (3 and 19) of β‐sinensal....

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Helvetica chimica acta 1967, Vol.50 (8), p.2445-2456
Hauptverfasser: Bertele, E., Schudel, P.
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 2456
container_issue 8
container_start_page 2445
container_title Helvetica chimica acta
container_volume 50
creator Bertele, E.
Schudel, P.
description β‐Sinensal (2,6‐dimethyl‐10‐methylene‐dodeca‐2,6,11‐trienal) was synthesized from the diene‐aldehyde 5. This was converted into the trans‐ and cis‐triene‐aldehydes 16 and 17, which were condensed with the phosphorane 18 to give the corresponding two geometrical isomers (3 and 19) of β‐sinensal.
doi_str_mv 10.1002/hlca.19670500830
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hlca_19670500830</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>HLCA19670500830</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1420-bd162b76555015b081ed3dd82a1249dda6d5ee6747a9ff9363ae339de0211bdd3</originalsourceid><addsrcrecordid>eNqFj71OwzAURi0EEqGwM-YFXO61YzseGKoIKFIkhoLEZjnxjRoUUhTzo2w8Aq8CD9KH4EmgKkM3pm_5zpEOY6cIUwQQZ8uu9lO02oACyCXssQSVEFxoo_ZZAoA5B7T3h-woxgcAsBZMwtLF-LykSOnrqk_Xn-lLH9L11_f7x6LtqY--O2YHje8infzthN1dXtwWc17eXF0Xs5LXmAngVUAtKqOVUoCqghwpyBBy4VFkNgSvgyLSJjPeNo2VWnqS0gYCgViFICcMtt56WMU4UOOehvbRD6NDcJtCtyl0O4W_yPkWeWs7Gv_9u3lZzHb5H3ftVw0</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Sythese von α und β‐Sinensal</title><source>Wiley Online Library Journals Frontfile Complete</source><creator>Bertele, E. ; Schudel, P.</creator><creatorcontrib>Bertele, E. ; Schudel, P.</creatorcontrib><description>β‐Sinensal (2,6‐dimethyl‐10‐methylene‐dodeca‐2,6,11‐trienal) was synthesized from the diene‐aldehyde 5. This was converted into the trans‐ and cis‐triene‐aldehydes 16 and 17, which were condensed with the phosphorane 18 to give the corresponding two geometrical isomers (3 and 19) of β‐sinensal.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.19670500830</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH</publisher><ispartof>Helvetica chimica acta, 1967, Vol.50 (8), p.2445-2456</ispartof><rights>Copyright © 1967 Verlag GmbH &amp; Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1420-bd162b76555015b081ed3dd82a1249dda6d5ee6747a9ff9363ae339de0211bdd3</citedby><cites>FETCH-LOGICAL-c1420-bd162b76555015b081ed3dd82a1249dda6d5ee6747a9ff9363ae339de0211bdd3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhlca.19670500830$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhlca.19670500830$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,4010,27900,27901,27902,45550,45551</link.rule.ids></links><search><creatorcontrib>Bertele, E.</creatorcontrib><creatorcontrib>Schudel, P.</creatorcontrib><title>Sythese von α und β‐Sinensal</title><title>Helvetica chimica acta</title><description>β‐Sinensal (2,6‐dimethyl‐10‐methylene‐dodeca‐2,6,11‐trienal) was synthesized from the diene‐aldehyde 5. This was converted into the trans‐ and cis‐triene‐aldehydes 16 and 17, which were condensed with the phosphorane 18 to give the corresponding two geometrical isomers (3 and 19) of β‐sinensal.</description><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1967</creationdate><recordtype>article</recordtype><recordid>eNqFj71OwzAURi0EEqGwM-YFXO61YzseGKoIKFIkhoLEZjnxjRoUUhTzo2w8Aq8CD9KH4EmgKkM3pm_5zpEOY6cIUwQQZ8uu9lO02oACyCXssQSVEFxoo_ZZAoA5B7T3h-woxgcAsBZMwtLF-LykSOnrqk_Xn-lLH9L11_f7x6LtqY--O2YHje8infzthN1dXtwWc17eXF0Xs5LXmAngVUAtKqOVUoCqghwpyBBy4VFkNgSvgyLSJjPeNo2VWnqS0gYCgViFICcMtt56WMU4UOOehvbRD6NDcJtCtyl0O4W_yPkWeWs7Gv_9u3lZzHb5H3ftVw0</recordid><startdate>1967</startdate><enddate>1967</enddate><creator>Bertele, E.</creator><creator>Schudel, P.</creator><general>WILEY‐VCH Verlag GmbH</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>1967</creationdate><title>Sythese von α und β‐Sinensal</title><author>Bertele, E. ; Schudel, P.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1420-bd162b76555015b081ed3dd82a1249dda6d5ee6747a9ff9363ae339de0211bdd3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1967</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bertele, E.</creatorcontrib><creatorcontrib>Schudel, P.</creatorcontrib><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bertele, E.</au><au>Schudel, P.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Sythese von α und β‐Sinensal</atitle><jtitle>Helvetica chimica acta</jtitle><date>1967</date><risdate>1967</risdate><volume>50</volume><issue>8</issue><spage>2445</spage><epage>2456</epage><pages>2445-2456</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>β‐Sinensal (2,6‐dimethyl‐10‐methylene‐dodeca‐2,6,11‐trienal) was synthesized from the diene‐aldehyde 5. This was converted into the trans‐ and cis‐triene‐aldehydes 16 and 17, which were condensed with the phosphorane 18 to give the corresponding two geometrical isomers (3 and 19) of β‐sinensal.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><doi>10.1002/hlca.19670500830</doi><tpages>12</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0018-019X
ispartof Helvetica chimica acta, 1967, Vol.50 (8), p.2445-2456
issn 0018-019X
1522-2675
language eng
recordid cdi_crossref_primary_10_1002_hlca_19670500830
source Wiley Online Library Journals Frontfile Complete
title Sythese von α und β‐Sinensal
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-13T14%3A52%3A11IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Sythese%20von%20%CE%B1%20und%20%CE%B2%E2%80%90Sinensal&rft.jtitle=Helvetica%20chimica%20acta&rft.au=Bertele,%20E.&rft.date=1967&rft.volume=50&rft.issue=8&rft.spage=2445&rft.epage=2456&rft.pages=2445-2456&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.19670500830&rft_dat=%3Cwiley_cross%3EHLCA19670500830%3C/wiley_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true