Gold(I)-catalyzed, stereocontrolled enamide synthesis from primary amides and propargyl aldehydes using a tandem strategy
DC Field | Value | Language |
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dc.contributor.author | Sang Min Kim | - |
dc.contributor.author | Dabon Lee | - |
dc.contributor.author | Soon Hyeok Hong | - |
dc.date.available | 2015-04-20T05:17:36Z | - |
dc.date.created | 2015-01-21 | - |
dc.date.issued | 2014-12 | - |
dc.identifier.issn | 1523-7060 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/854 | - |
dc.description.abstract | A novel strategy for enamide synthesis from primary amides and propargyl aldehydes via Au(I)-catalyzed tandem amide addition and Meyer−Schuster rearrangement is described. In situ generated hemiaminals were successfully converted to the desired products under the optimized conditions. Enamide stereochemistry was controlled simply by changing solvents and adding a catalytic amount of acid. The developed synthetic strategy provides a new method to synthesize various β-substituted α,β-unsaturated carbonyl compounds. | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | AMER CHEMICAL SOC | - |
dc.title | Gold(I)-catalyzed, stereocontrolled enamide synthesis from primary amides and propargyl aldehydes using a tandem strategy | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000346037500033 | - |
dc.identifier.scopusid | 2-s2.0-84916222865 | - |
dc.identifier.rimsid | 16952 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Sang Min Kim | - |
dc.contributor.affiliatedAuthor | Dabon Lee | - |
dc.contributor.affiliatedAuthor | Soon Hyeok Hong | - |
dc.identifier.doi | 10.1021/ol503055x | - |
dc.identifier.bibliographicCitation | ORGANIC LETTERS, v.16, no.23, pp.6168 - 6171 | - |
dc.citation.title | ORGANIC LETTERS | - |
dc.citation.volume | 16 | - |
dc.citation.number | 23 | - |
dc.citation.startPage | 6168 | - |
dc.citation.endPage | 6171 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 14 | - |
dc.description.scptc | 16 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |