HIGHLY DIASTEREOSELECTIVE REDUCTION OF NEW CHIRAL ALPHA-KETOAMIDES
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | BYUN, IS | ko |
| dc.contributor.author | Kim, Yong Hae | ko |
| dc.date.accessioned | 2013-02-28T02:33:40Z | - |
| dc.date.available | 2013-02-28T02:33:40Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1995 | - |
| dc.identifier.citation | SYNTHETIC COMMUNICATIONS, v.25, no.13, pp.1963 - 1969 | - |
| dc.identifier.issn | 0039-7911 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/72314 | - |
| dc.description.abstract | Both pyruvamide and benzoylformamide having (S)-2-methoxymethylindoline as a chiral auxiliary were reduced with various reducing agents in high stereoselectivities (up to dr = 99 : 1). | - |
| dc.language | English | - |
| dc.publisher | MARCEL DEKKER INC | - |
| dc.subject | ASYMMETRIC-SYNTHESIS | - |
| dc.subject | KETO AMIDES | - |
| dc.subject | AMINO ACIDS | - |
| dc.subject | AUXILIARIES | - |
| dc.subject | ESTERS | - |
| dc.title | HIGHLY DIASTEREOSELECTIVE REDUCTION OF NEW CHIRAL ALPHA-KETOAMIDES | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1995QY01200010 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 25 | - |
| dc.citation.issue | 13 | - |
| dc.citation.beginningpage | 1963 | - |
| dc.citation.endingpage | 1969 | - |
| dc.citation.publicationname | SYNTHETIC COMMUNICATIONS | - |
| dc.identifier.doi | 10.1080/00397919508015873 | - |
| dc.contributor.nonIdAuthor | BYUN, IS | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | ASYMMETRIC-SYNTHESIS | - |
| dc.subject.keywordPlus | KETO AMIDES | - |
| dc.subject.keywordPlus | AMINO ACIDS | - |
| dc.subject.keywordPlus | AUXILIARIES | - |
| dc.subject.keywordPlus | ESTERS | - |
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