Pyridinium Ylides in the Synthesis of 2,3-Dihydrofurans
ABSTRACT A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency o...
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| Veröffentlicht in: | Synthesis (Stuttgart) 2006-02, Vol.2006 (4), p.675-679 |
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| container_end_page | 679 |
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| container_issue | 4 |
| container_start_page | 675 |
| container_title | Synthesis (Stuttgart) |
| container_volume | 2006 |
| creator | Chuang, Che-Ping Tsai, An-I |
| description | ABSTRACT
A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency of this reaction the one-pot process was also developed, in which the pyridinium salts were generated in situ from corresponding halides. |
| doi_str_mv | 10.1055/s-2006-926300 |
| format | Article |
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A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency of this reaction the one-pot process was also developed, in which the pyridinium salts were generated in situ from corresponding halides.</description><identifier>ISSN: 0039-7881</identifier><identifier>EISSN: 1437-210X</identifier><identifier>DOI: 10.1055/s-2006-926300</identifier><language>eng</language><ispartof>Synthesis (Stuttgart), 2006-02, Vol.2006 (4), p.675-679</ispartof><rights>Georg Thieme Verlag Stuttgart · New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c236t-e1b4cca5ee5a93312aec6b08d864312f5462d2b39eb207c06e7fe8fdaeca4e6a3</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-2006-926300.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2006-926300$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,27903,27904,54537,54538</link.rule.ids></links><search><creatorcontrib>Chuang, Che-Ping</creatorcontrib><creatorcontrib>Tsai, An-I</creatorcontrib><title>Pyridinium Ylides in the Synthesis of 2,3-Dihydrofurans</title><title>Synthesis (Stuttgart)</title><addtitle>Synthesis</addtitle><description>ABSTRACT
A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency of this reaction the one-pot process was also developed, in which the pyridinium salts were generated in situ from corresponding halides.</description><issn>0039-7881</issn><issn>1437-210X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNotj01LxDAURYMoWEeX7vMDJvqS1ybtUsZPGFBQQVchbV5ohpkWmnbRf2-HcXW4cLmXw9ithDsJRXGfhALQolIaAc5YJnM0Qkn4OWcZAFbClKW8ZFcp7QDAKKwyZj7mIfrYxenAf_fRU-Kx42NL_HPuFqSYeB-4WqN4jO3shz5Mg-vSNbsIbp_o5p8r9v389LV5Fdv3l7fNw1Y0CvUoSNZ507iCqHAVolSOGl1D6UudLykUuVZe1VhRrcA0oMkEKoNfai4n7XDF1qfdsY10ILvrp6FbDq0Ee5S2yR6l7Uka_wDZ6knq</recordid><startdate>20060215</startdate><enddate>20060215</enddate><creator>Chuang, Che-Ping</creator><creator>Tsai, An-I</creator><scope/></search><sort><creationdate>20060215</creationdate><title>Pyridinium Ylides in the Synthesis of 2,3-Dihydrofurans</title><author>Chuang, Che-Ping ; Tsai, An-I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c236t-e1b4cca5ee5a93312aec6b08d864312f5462d2b39eb207c06e7fe8fdaeca4e6a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chuang, Che-Ping</creatorcontrib><creatorcontrib>Tsai, An-I</creatorcontrib><jtitle>Synthesis (Stuttgart)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Chuang, Che-Ping</au><au>Tsai, An-I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Pyridinium Ylides in the Synthesis of 2,3-Dihydrofurans</atitle><jtitle>Synthesis (Stuttgart)</jtitle><addtitle>Synthesis</addtitle><date>2006-02-15</date><risdate>2006</risdate><volume>2006</volume><issue>4</issue><spage>675</spage><epage>679</epage><pages>675-679</pages><issn>0039-7881</issn><eissn>1437-210X</eissn><abstract>ABSTRACT
A new method for the synthesis of 2,3-dihydrofurans from readily available starting enones and pyridinium salts has been developed. This protocol can provide a novel and effective methodology for the preparation of 2,3-dihydrofurans in a stereoselective fashion. To increase the efficiency of this reaction the one-pot process was also developed, in which the pyridinium salts were generated in situ from corresponding halides.</abstract><doi>10.1055/s-2006-926300</doi><tpages>5</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0039-7881 |
| ispartof | Synthesis (Stuttgart), 2006-02, Vol.2006 (4), p.675-679 |
| issn | 0039-7881 1437-210X |
| language | eng |
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| source | Thieme Connect Journals |
| title | Pyridinium Ylides in the Synthesis of 2,3-Dihydrofurans |
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