Facile Nucleophilic Substitution of 3-tert-Butyldimethylsilyloxyalk-2-enyl-phosphonium Salts
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Sung Gak | ko |
| dc.date.accessioned | 2013-02-28T00:09:17Z | - |
| dc.date.available | 2013-02-28T00:09:17Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1999-09 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.40, no.38, pp.6975 - 6978 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/71643 | - |
| dc.description.abstract | Phosphoniosilylation of alpha,beta-enones with TBSOTf and triphenylphosphine at 0 degrees C affords 3-tert-butyldimethylsilyloxyalk-2-enylphosphonium salts, which undergo facile nucleophilic substitution with various nucleophiles to give 3-substituted silyl enol ethers in good yields. (C) 1999 Elsevier Science Ltd. All rights reserved. | - |
| dc.language | English | - |
| dc.publisher | Pergamon-Elsevier Science Ltd | - |
| dc.subject | CONJUGATE ADDITION | - |
| dc.subject | ENONES | - |
| dc.subject | PHOSPHONIOSILYLATION | - |
| dc.title | Facile Nucleophilic Substitution of 3-tert-Butyldimethylsilyloxyalk-2-enyl-phosphonium Salts | - |
| dc.type | Article | - |
| dc.identifier.wosid | 000082402600025 | - |
| dc.identifier.scopusid | 2-s2.0-0033578639 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 40 | - |
| dc.citation.issue | 38 | - |
| dc.citation.beginningpage | 6975 | - |
| dc.citation.endingpage | 6978 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.contributor.localauthor | Kim, Sung Gak | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordAuthor | phosphoniosilylation | - |
| dc.subject.keywordAuthor | nucleophilic substitution | - |
| dc.subject.keywordAuthor | 3-substituted silyl enol ether | - |
| dc.subject.keywordPlus | CONJUGATE ADDITION | - |
| dc.subject.keywordPlus | ENONES | - |
| dc.subject.keywordPlus | PHOSPHONIOSILYLATION | - |
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