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1,2-Ferrocenediylazaphosphinines 2: A New Class of Nucleophilic Catalysts for Ring-Opening of Epoxides
Abstract 1,2-Ferrocenediylazaphosphinines (1A-C) have been successfully employed as a new class of nucleophilic catalysts for ring-opening of a range of epoxides, their catalytic efficiency in terms of regioselectivity as well as chemical yield comparing well with the existing catalysts in the liter...
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Published in: | Synlett 2003-05, Vol.2003 (6) |
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container_issue | 6 |
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container_title | Synlett |
container_volume | 2003 |
creator | Paek, Seung Hwan Shim, Sang Chul Cho, Chan Sik Kim, Tae-Jeong |
description | Abstract
1,2-Ferrocenediylazaphosphinines (1A-C) have been successfully employed as a
new class of nucleophilic catalysts for ring-opening of a range
of epoxides, their catalytic efficiency in terms of regioselectivity
as well as chemical yield comparing well with the existing catalysts
in the literature. In contrast, low enantiomeric excesses have been
obtained from the reactions of MESO-epoxides
catalyzed by (R)-1. |
doi_str_mv | 10.1055/s-2003-38758 |
format | article |
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1,2-Ferrocenediylazaphosphinines (1A-C) have been successfully employed as a
new class of nucleophilic catalysts for ring-opening of a range
of epoxides, their catalytic efficiency in terms of regioselectivity
as well as chemical yield comparing well with the existing catalysts
in the literature. In contrast, low enantiomeric excesses have been
obtained from the reactions of MESO-epoxides
catalyzed by (R)-1.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2003-38758</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2003-05, Vol.2003 (6)</ispartof><rights>Georg Thieme Verlag Stuttgart ˙ New York</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></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-2003-38758.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2003-38758$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3005,27901,27902,54534,54535</link.rule.ids></links><search><creatorcontrib>Paek, Seung Hwan</creatorcontrib><creatorcontrib>Shim, Sang Chul</creatorcontrib><creatorcontrib>Cho, Chan Sik</creatorcontrib><creatorcontrib>Kim, Tae-Jeong</creatorcontrib><title>1,2-Ferrocenediylazaphosphinines 2: A New Class of Nucleophilic Catalysts for Ring-Opening of Epoxides</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
1,2-Ferrocenediylazaphosphinines (1A-C) have been successfully employed as a
new class of nucleophilic catalysts for ring-opening of a range
of epoxides, their catalytic efficiency in terms of regioselectivity
as well as chemical yield comparing well with the existing catalysts
in the literature. In contrast, low enantiomeric excesses have been
obtained from the reactions of MESO-epoxides
catalyzed by (R)-1.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNotkF1LwzAYhYMoOKd3_oDcazTfbbwbZVNhbCB6XdI2WTNqU_p26PbrbdWrA4fzAQ9Ct4w-MKrUIxBOqSAiTVR6hmZMimR0jD5HM2qEJoozeYmuAPaUMpkaOkOe3XOycn0fS9e6Khwbe7JdHaGrQxtaB5g_4QXeuC-cNRYAR483h7JxcQw0ocSZHWxzhAGwjz1-C-2ObDs3VndTdNnF71A5uEYX3jbgbv51jj5Wy_fshay3z6_ZYk2ApWYghkslpdGldq5Kk9IURlCV2Irp1GhqvbZK2MIbz7ignvOiMJ57pq2oElNIMUd3f7tDHdyny_fx0LfjYc5oPiHKIZ8Q5b-IxA8MLFlE</recordid><startdate>20030505</startdate><enddate>20030505</enddate><creator>Paek, Seung Hwan</creator><creator>Shim, Sang Chul</creator><creator>Cho, Chan Sik</creator><creator>Kim, Tae-Jeong</creator><scope/></search><sort><creationdate>20030505</creationdate><title>1,2-Ferrocenediylazaphosphinines 2: A New Class of Nucleophilic Catalysts for Ring-Opening of Epoxides</title><author>Paek, Seung Hwan ; Shim, Sang Chul ; Cho, Chan Sik ; Kim, Tae-Jeong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-s189t-92454496c6eed87c9b93057ad168960af6a53abf9f1230f22bb9f2f16a3d79b43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Paek, Seung Hwan</creatorcontrib><creatorcontrib>Shim, Sang Chul</creatorcontrib><creatorcontrib>Cho, Chan Sik</creatorcontrib><creatorcontrib>Kim, Tae-Jeong</creatorcontrib><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Paek, Seung Hwan</au><au>Shim, Sang Chul</au><au>Cho, Chan Sik</au><au>Kim, Tae-Jeong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1,2-Ferrocenediylazaphosphinines 2: A New Class of Nucleophilic Catalysts for Ring-Opening of Epoxides</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2003-05-05</date><risdate>2003</risdate><volume>2003</volume><issue>6</issue><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
1,2-Ferrocenediylazaphosphinines (1A-C) have been successfully employed as a
new class of nucleophilic catalysts for ring-opening of a range
of epoxides, their catalytic efficiency in terms of regioselectivity
as well as chemical yield comparing well with the existing catalysts
in the literature. In contrast, low enantiomeric excesses have been
obtained from the reactions of MESO-epoxides
catalyzed by (R)-1.</abstract><doi>10.1055/s-2003-38758</doi></addata></record> |
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title | 1,2-Ferrocenediylazaphosphinines 2: A New Class of Nucleophilic Catalysts for Ring-Opening of Epoxides |
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