The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones
The one electron electrochemical reduction of α,β-unsaturated ketones 2 is a useful method of establishing carbon to carbon bonds. For example 3 , it has been utilized in an intramolecular coupling to generate the perhydrophenanthrene ring system in the reduction of 1 to 2:
Gespeichert in:
Veröffentlicht in: | Synthetic communications 1981-01, Vol.11 (1), p.55-59 |
---|---|
Hauptverfasser: | , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 59 |
---|---|
container_issue | 1 |
container_start_page | 55 |
container_title | Synthetic communications |
container_volume | 11 |
creator | Mandell, Leon Heldrich, F. J. Day, R. A. |
description | The one electron electrochemical reduction of α,β-unsaturated ketones
2
is a useful method of establishing carbon to carbon bonds. For example
3
, it has been utilized in an intramolecular coupling to generate the perhydrophenanthrene ring system in the reduction of 1 to 2: |
doi_str_mv | 10.1080/00397918108064282 |
format | Article |
fullrecord | <record><control><sourceid>crossref_infor</sourceid><recordid>TN_cdi_crossref_primary_10_1080_00397918108064282</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_00397918108064282</sourcerecordid><originalsourceid>FETCH-LOGICAL-c228t-db6fb1d3165be8c11bd05c99fe08d480f6aece53e8ecc587924586fd178f52663</originalsourceid><addsrcrecordid>eNp1kE1OwzAQhS0EEqVwAHa5gME_seNIbFAJfypCQmUdOfaYGty4sgOo1-IgnIlGZYdYjea99430BqFTSs4oUeScEF5XNVXjIkum2B6aUMEZZiVn-2gy-ngboIfoKOdXQqioVD1B94slFE0AM6RolrDyRofiCey7GfwHFLP4vg6-fymiKx5iH3HTx1A0wxJSHrXvL3zl32CIPeRjdOB0yHDyO6fo-bpZzG7x_PHmbnY5x4YxNWDbSddRy6kUHShDaWeJMHXtgChbKuKkBgOCgwJjhKpqVgolnaWVcoJJyaeI7u6aFHNO4Np18iudNi0l7di__fOMLXOxY3zvYlrpz5iCbQe9CTG5pHvjc8v_x38AFAFlVg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones</title><source>Taylor & Francis Journals Complete</source><creator>Mandell, Leon ; Heldrich, F. J. ; Day, R. A.</creator><creatorcontrib>Mandell, Leon ; Heldrich, F. J. ; Day, R. A.</creatorcontrib><description>The one electron electrochemical reduction of α,β-unsaturated ketones
2
is a useful method of establishing carbon to carbon bonds. For example
3
, it has been utilized in an intramolecular coupling to generate the perhydrophenanthrene ring system in the reduction of 1 to 2:</description><identifier>ISSN: 0039-7911</identifier><identifier>EISSN: 1532-2432</identifier><identifier>DOI: 10.1080/00397918108064282</identifier><language>eng</language><publisher>Taylor & Francis Group</publisher><ispartof>Synthetic communications, 1981-01, Vol.11 (1), p.55-59</ispartof><rights>Copyright Taylor & Francis Group, LLC 1981</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c228t-db6fb1d3165be8c11bd05c99fe08d480f6aece53e8ecc587924586fd178f52663</citedby><cites>FETCH-LOGICAL-c228t-db6fb1d3165be8c11bd05c99fe08d480f6aece53e8ecc587924586fd178f52663</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00397918108064282$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00397918108064282$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,780,784,27924,27925,59647,60436</link.rule.ids></links><search><creatorcontrib>Mandell, Leon</creatorcontrib><creatorcontrib>Heldrich, F. J.</creatorcontrib><creatorcontrib>Day, R. A.</creatorcontrib><title>The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones</title><title>Synthetic communications</title><description>The one electron electrochemical reduction of α,β-unsaturated ketones
2
is a useful method of establishing carbon to carbon bonds. For example
3
, it has been utilized in an intramolecular coupling to generate the perhydrophenanthrene ring system in the reduction of 1 to 2:</description><issn>0039-7911</issn><issn>1532-2432</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1981</creationdate><recordtype>article</recordtype><recordid>eNp1kE1OwzAQhS0EEqVwAHa5gME_seNIbFAJfypCQmUdOfaYGty4sgOo1-IgnIlGZYdYjea99430BqFTSs4oUeScEF5XNVXjIkum2B6aUMEZZiVn-2gy-ngboIfoKOdXQqioVD1B94slFE0AM6RolrDyRofiCey7GfwHFLP4vg6-fymiKx5iH3HTx1A0wxJSHrXvL3zl32CIPeRjdOB0yHDyO6fo-bpZzG7x_PHmbnY5x4YxNWDbSddRy6kUHShDaWeJMHXtgChbKuKkBgOCgwJjhKpqVgolnaWVcoJJyaeI7u6aFHNO4Np18iudNi0l7di__fOMLXOxY3zvYlrpz5iCbQe9CTG5pHvjc8v_x38AFAFlVg</recordid><startdate>19810101</startdate><enddate>19810101</enddate><creator>Mandell, Leon</creator><creator>Heldrich, F. J.</creator><creator>Day, R. A.</creator><general>Taylor & Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19810101</creationdate><title>The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones</title><author>Mandell, Leon ; Heldrich, F. J. ; Day, R. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c228t-db6fb1d3165be8c11bd05c99fe08d480f6aece53e8ecc587924586fd178f52663</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1981</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mandell, Leon</creatorcontrib><creatorcontrib>Heldrich, F. J.</creatorcontrib><creatorcontrib>Day, R. A.</creatorcontrib><collection>CrossRef</collection><jtitle>Synthetic communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mandell, Leon</au><au>Heldrich, F. J.</au><au>Day, R. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones</atitle><jtitle>Synthetic communications</jtitle><date>1981-01-01</date><risdate>1981</risdate><volume>11</volume><issue>1</issue><spage>55</spage><epage>59</epage><pages>55-59</pages><issn>0039-7911</issn><eissn>1532-2432</eissn><abstract>The one electron electrochemical reduction of α,β-unsaturated ketones
2
is a useful method of establishing carbon to carbon bonds. For example
3
, it has been utilized in an intramolecular coupling to generate the perhydrophenanthrene ring system in the reduction of 1 to 2:</abstract><pub>Taylor & Francis Group</pub><doi>10.1080/00397918108064282</doi><tpages>5</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0039-7911 |
ispartof | Synthetic communications, 1981-01, Vol.11 (1), p.55-59 |
issn | 0039-7911 1532-2432 |
language | eng |
recordid | cdi_crossref_primary_10_1080_00397918108064282 |
source | Taylor & Francis Journals Complete |
title | The Electrochemical Reductive Coupling of Mono-Enol Ethers of β-Diketones |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T15%3A32%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Electrochemical%20Reductive%20Coupling%20of%20Mono-Enol%20Ethers%20of%20%CE%B2-Diketones&rft.jtitle=Synthetic%20communications&rft.au=Mandell,%20Leon&rft.date=1981-01-01&rft.volume=11&rft.issue=1&rft.spage=55&rft.epage=59&rft.pages=55-59&rft.issn=0039-7911&rft.eissn=1532-2432&rft_id=info:doi/10.1080/00397918108064282&rft_dat=%3Ccrossref_infor%3E10_1080_00397918108064282%3C/crossref_infor%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 |