DC Field | Value | Language |
---|---|---|
dc.contributor.author | Kim, Yong Hae | ko |
dc.contributor.author | BYUN, IS | ko |
dc.contributor.author | CHOI, JY | ko |
dc.date.accessioned | 2013-02-28T02:33:12Z | - |
dc.date.available | 2013-02-28T02:33:12Z | - |
dc.date.created | 2012-02-06 | - |
dc.date.created | 2012-02-06 | - |
dc.date.issued | 1995-05 | - |
dc.identifier.citation | TETRAHEDRON-ASYMMETRY, v.6, no.5, pp.1025 - 1026 | - |
dc.identifier.issn | 0957-4166 | - |
dc.identifier.uri | http://hdl.handle.net/10203/72312 | - |
dc.description.abstract | The stereocontrolled nucleophilic addition of organametallics to novel chiral alpha-ketoamides which were synthesized from (S)-2-methoxymethylindoline as a chiral auxiliary was carried out to obtain alpha-hydroxyamides with extremely high diastereoselectivities ( up to dr greater than or equal to 99:1). | - |
dc.language | English | - |
dc.publisher | PERGAMON-ELSEVIER SCIENCE LTD | - |
dc.subject | ASYMMETRIC-SYNTHESIS | - |
dc.subject | KETO AMIDES | - |
dc.subject | AMINO ACIDS | - |
dc.subject | REDUCTION | - |
dc.subject | ALCOHOLS | - |
dc.subject | ESTERS | - |
dc.title | HIGHLY DIASTEREOSELECTIVE ADDITION OF ORGANOMETALLICS TO NOVEL CHIRAL ALPHA-KETOAMIDES OF (S)-2-METHOXYMETHYLINDOLINE | - |
dc.type | Article | - |
dc.identifier.wosid | A1995RB58300003 | - |
dc.type.rims | ART | - |
dc.citation.volume | 6 | - |
dc.citation.issue | 5 | - |
dc.citation.beginningpage | 1025 | - |
dc.citation.endingpage | 1026 | - |
dc.citation.publicationname | TETRAHEDRON-ASYMMETRY | - |
dc.identifier.doi | 10.1016/0957-4166(95)00115-6 | - |
dc.contributor.nonIdAuthor | BYUN, IS | - |
dc.contributor.nonIdAuthor | CHOI, JY | - |
dc.type.journalArticle | Note | - |
dc.subject.keywordPlus | ASYMMETRIC-SYNTHESIS | - |
dc.subject.keywordPlus | KETO AMIDES | - |
dc.subject.keywordPlus | AMINO ACIDS | - |
dc.subject.keywordPlus | REDUCTION | - |
dc.subject.keywordPlus | ALCOHOLS | - |
dc.subject.keywordPlus | ESTERS | - |
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