Highly Chemoselective Allylation of Aldehydes in the Presence of Ketones
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Sung Gak | ko |
| dc.date.accessioned | 2013-02-28T02:21:37Z | - |
| dc.date.available | 2013-02-28T02:21:37Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1995-03 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.36, no.21, pp.3723 - 3724 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/72260 | - |
| dc.description.abstract | Highly chemoselective allylation of aldehydes in the presence of ketones has been achieved by preferential in situ conversion of aldehydes into 1-silyloxysulfonium salts and subsequent displacement with allyltributyltin | - |
| dc.language | English | - |
| dc.publisher | Pergamon-Elsevier Science Ltd | - |
| dc.subject | CARBONYL-COMPOUNDS | - |
| dc.title | Highly Chemoselective Allylation of Aldehydes in the Presence of Ketones | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1995RA22400035 | - |
| dc.identifier.scopusid | 2-s2.0-0029012557 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 36 | - |
| dc.citation.issue | 21 | - |
| dc.citation.beginningpage | 3723 | - |
| dc.citation.endingpage | 3724 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.contributor.localauthor | Kim, Sung Gak | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | CARBONYL-COMPOUNDS | - |
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