HIGHLY STEREOSELECTIVE ALLYLATION TO CHIRAL ALPHA-KETO AMIDES DERIVED FROM (S)-INDOLINE-2-CARBOXYLIC ACID - ASYMMETRIC-SYNTHESIS OF FUNCTIONALIZED TERTIARY HOMOALLYL ALCOHOLS
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Kim, Yong Hae | ko |
| dc.contributor.author | KIM, SH | ko |
| dc.date.accessioned | 2013-02-28T04:39:55Z | - |
| dc.date.available | 2013-02-28T04:39:55Z | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.created | 2012-02-06 | - |
| dc.date.issued | 1995-09 | - |
| dc.identifier.citation | TETRAHEDRON LETTERS, v.36, no.38, pp.6895 - 6898 | - |
| dc.identifier.issn | 0040-4039 | - |
| dc.identifier.uri | http://hdl.handle.net/10203/72816 | - |
| dc.description.abstract | The diastereoselective addition of allylsilane and - stannane in the presence of Lewis acids to new chiral alpha-keto amides derived from (S)-indoline-2-carboxylic acid resulted in optically active tertiary homoallyl alcohols 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 | DIASTEREOSELECTIVE ADDITION | - |
| dc.subject | ORGANOMETALLICS | - |
| dc.subject | ESTERS | - |
| dc.title | HIGHLY STEREOSELECTIVE ALLYLATION TO CHIRAL ALPHA-KETO AMIDES DERIVED FROM (S)-INDOLINE-2-CARBOXYLIC ACID - ASYMMETRIC-SYNTHESIS OF FUNCTIONALIZED TERTIARY HOMOALLYL ALCOHOLS | - |
| dc.type | Article | - |
| dc.identifier.wosid | A1995RV68400025 | - |
| dc.type.rims | ART | - |
| dc.citation.volume | 36 | - |
| dc.citation.issue | 38 | - |
| dc.citation.beginningpage | 6895 | - |
| dc.citation.endingpage | 6898 | - |
| dc.citation.publicationname | TETRAHEDRON LETTERS | - |
| dc.identifier.doi | 10.1016/0040-4039(95)01424-G | - |
| dc.contributor.nonIdAuthor | KIM, SH | - |
| dc.type.journalArticle | Article | - |
| dc.subject.keywordPlus | DIASTEREOSELECTIVE ADDITION | - |
| dc.subject.keywordPlus | ORGANOMETALLICS | - |
| dc.subject.keywordPlus | ESTERS | - |
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