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Asymmetric Cyanosilylation of Ketones Catalyzed by Chiral N-Oxide-titanium (IV) Complex
Abstract A new approach for the asymmetric addition of trimethylsilylcyanide to ketones using chiral N-oxide-Ti(IPrO) 4 complex as catalyst is reported. The screening of a number of chiral N-oxides has resulted in a system that gives the O-TMS ethers of cyanohydrins in good isolated yields with ena...
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Published in: | Synlett 2002, Vol.2002 (8), p.1353-1355 |
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container_end_page | 1355 |
container_issue | 8 |
container_start_page | 1353 |
container_title | Synlett |
container_volume | 2002 |
creator | Shen, Yongcun Feng, Xiaoming Zhang, Guolin Jiang, Yaozhong |
description | Abstract
A new approach for the asymmetric addition of trimethylsilylcyanide
to ketones using chiral N-oxide-Ti(IPrO)
4
complex as catalyst
is reported. The screening of a number of chiral N-oxides has
resulted in a system that gives the O-TMS ethers of cyanohydrins
in good isolated yields with enantiomeric excesses of up to 69%. |
doi_str_mv | 10.1055/s-2002-32983 |
format | article |
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A new approach for the asymmetric addition of trimethylsilylcyanide
to ketones using chiral N-oxide-Ti(IPrO)
4
complex as catalyst
is reported. The screening of a number of chiral N-oxides has
resulted in a system that gives the O-TMS ethers of cyanohydrins
in good isolated yields with enantiomeric excesses of up to 69%.</description><identifier>ISSN: 0936-5214</identifier><identifier>EISSN: 1437-2096</identifier><identifier>DOI: 10.1055/s-2002-32983</identifier><language>eng</language><subject>letter</subject><ispartof>Synlett, 2002, Vol.2002 (8), p.1353-1355</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-2002-32983.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2002-32983$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,780,784,3017,3018,4024,27923,27924,27925,54559,54560</link.rule.ids></links><search><creatorcontrib>Shen, Yongcun</creatorcontrib><creatorcontrib>Feng, Xiaoming</creatorcontrib><creatorcontrib>Zhang, Guolin</creatorcontrib><creatorcontrib>Jiang, Yaozhong</creatorcontrib><title>Asymmetric Cyanosilylation of Ketones Catalyzed by Chiral N-Oxide-titanium (IV) Complex</title><title>Synlett</title><addtitle>Synlett</addtitle><description>Abstract
A new approach for the asymmetric addition of trimethylsilylcyanide
to ketones using chiral N-oxide-Ti(IPrO)
4
complex as catalyst
is reported. The screening of a number of chiral N-oxides has
resulted in a system that gives the O-TMS ethers of cyanohydrins
in good isolated yields with enantiomeric excesses of up to 69%.</description><subject>letter</subject><issn>0936-5214</issn><issn>1437-2096</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><recordid>eNptkEtLAzEUhYMoWKs7f0CWikZvkpnpZFkGH8ViNz6Ww80kQ1PmUZIUOv56p-rS1YHDx-HwEXLJ4Y5Dmt4HJgAEk0Ll8ohMeCJnY6OyYzIBJTOWCp6ckrMQNgA8yRVMyOc8DG1ro3cVLQbs-uCaocHo-o72NX2xse9soAVGbIYva6geaLF2Hhv6ylZ7ZyyLLmLndi29Wnxc06Jvt43dn5OTGptgL_5ySt4fH96KZ7ZcPS2K-ZJVQmRxvCq5yrkGCwJyo61BJW0msgy1TnhiJK-F1mgqww1gCgZzhXkFuZwptEpOye3vbuX7ELyty613Lfqh5FAepJShPEgpf6SM-M0vHtfOtrbc9Dvfjf_-p78Br0Niog</recordid><startdate>2002</startdate><enddate>2002</enddate><creator>Shen, Yongcun</creator><creator>Feng, Xiaoming</creator><creator>Zhang, Guolin</creator><creator>Jiang, Yaozhong</creator><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>2002</creationdate><title>Asymmetric Cyanosilylation of Ketones Catalyzed by Chiral N-Oxide-titanium (IV) Complex</title><author>Shen, Yongcun ; Feng, Xiaoming ; Zhang, Guolin ; Jiang, Yaozhong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c226t-3231981b0e0208dbeda93e6266abb414d31f2bbadcd1d0a50da89a8c08379ae93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>letter</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shen, Yongcun</creatorcontrib><creatorcontrib>Feng, Xiaoming</creatorcontrib><creatorcontrib>Zhang, Guolin</creatorcontrib><creatorcontrib>Jiang, Yaozhong</creatorcontrib><collection>CrossRef</collection><jtitle>Synlett</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shen, Yongcun</au><au>Feng, Xiaoming</au><au>Zhang, Guolin</au><au>Jiang, Yaozhong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric Cyanosilylation of Ketones Catalyzed by Chiral N-Oxide-titanium (IV) Complex</atitle><jtitle>Synlett</jtitle><addtitle>Synlett</addtitle><date>2002</date><risdate>2002</risdate><volume>2002</volume><issue>8</issue><spage>1353</spage><epage>1355</epage><pages>1353-1355</pages><issn>0936-5214</issn><eissn>1437-2096</eissn><abstract>Abstract
A new approach for the asymmetric addition of trimethylsilylcyanide
to ketones using chiral N-oxide-Ti(IPrO)
4
complex as catalyst
is reported. The screening of a number of chiral N-oxides has
resulted in a system that gives the O-TMS ethers of cyanohydrins
in good isolated yields with enantiomeric excesses of up to 69%.</abstract><doi>10.1055/s-2002-32983</doi><tpages>3</tpages></addata></record> |
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subjects | letter |
title | Asymmetric Cyanosilylation of Ketones Catalyzed by Chiral N-Oxide-titanium (IV) Complex |
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