DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Sung Gak | ko |
dc.contributor.author | Yoon, JY | ko |
dc.contributor.author | Lee, IY | ko |
dc.date.accessioned | 2013-03-02T16:08:07Z | - |
dc.date.available | 2013-03-02T16:08:07Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1997-05 | - |
dc.identifier.citation | SYNLETT, pp.475 - 475 | - |
dc.identifier.issn | 0936-5214 | - |
dc.identifier.uri | http://hdl.handle.net/10203/74346 | - |
dc.description.abstract | A new efficient method for the preparation of alpha-keto esters via a free radical acylation approach using phenylsulfonyl methoxycarbonyl oxime ether 1 has been developed. When an alkyl iodide was treated with 1, hexamethylditin, and acetone in THF at 300 nm for 3 h, alpha-keto ester 3 was obtained in high yield after hydrolysis of the oxime ether 2. | - |
dc.language | English | - |
dc.publisher | GEORG THIEME VERLAG | - |
dc.title | Facile synthesis of alpha-keto esters via a free radical acylation approach | - |
dc.type | Article | - |
dc.identifier.wosid | A1997XD87200023 | - |
dc.type.rims | ART | - |
dc.citation.beginningpage | 475 | - |
dc.citation.endingpage | 475 | - |
dc.citation.publicationname | SYNLETT | - |
dc.contributor.localauthor | Kim, Sung Gak | - |
dc.contributor.nonIdAuthor | Yoon, JY | - |
dc.contributor.nonIdAuthor | Lee, IY | - |
dc.type.journalArticle | Article | - |
dc.subject.keywordAuthor | alpha-keto esters | - |
dc.subject.keywordAuthor | phenylsulfonyl methoxycarbonyl oxime ether | - |
dc.subject.keywordAuthor | free radical acylation | - |
dc.subject.keywordAuthor | tandem radical reaction | - |
dc.subject.keywordPlus | OMEGA-FORMYLALKYL RADICALS | - |
dc.subject.keywordPlus | CARBON RADICALS | - |
dc.subject.keywordPlus | CYCLIZATION | - |
dc.subject.keywordPlus | KETOESTERS | - |
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