Cited 81 time in
Gold-Catalyzed Synthesis of 3-Pyrrolidinones and Nitrones from N-Sulfonyl Hydroxylamines via Oxygen-Transfer Redox and 1,3-Sulfonyl Migration
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Yeom, Hyun-Suk | - |
| dc.contributor.author | So, Eunsu | - |
| dc.contributor.author | Shin, Seunghoon | - |
| dc.date.accessioned | 2022-07-07T14:13:21Z | - |
| dc.date.available | 2022-07-07T14:13:21Z | - |
| dc.date.issued | 2011-12 | - |
| dc.identifier.issn | 0947-6539 | - |
| dc.identifier.issn | 1521-3765 | - |
| dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/144812 | - |
| dc.description.abstract | Golden touch: Gold-catalyzed reaction of N-sulfonyl hydroxylamines with terminal alkyne led to 3-pyrrolidinones by means of an oygen-transfer redox reaction. This protocol constitutes a direct method for forming α-amino carbonyl compounds. In sharp contrast, those with internal alkynes underwent 1,3-sulfonyl migration leading to 3-sulfonyl cyclic nitrones. | - |
| dc.format.extent | 4 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | John Wiley & Sons Ltd. | - |
| dc.title | Gold-Catalyzed Synthesis of 3-Pyrrolidinones and Nitrones from N-Sulfonyl Hydroxylamines via Oxygen-Transfer Redox and 1,3-Sulfonyl Migration | - |
| dc.type | Article | - |
| dc.publisher.location | 독일 | - |
| dc.identifier.doi | 10.1002/chem.201002863 | - |
| dc.identifier.scopusid | 2-s2.0-79551480829 | - |
| dc.identifier.wosid | 000287787100003 | - |
| dc.identifier.bibliographicCitation | Chemistry - A European Journal, v.17, no.6, pp 1764 - 1767 | - |
| dc.citation.title | Chemistry - A European Journal | - |
| dc.citation.volume | 17 | - |
| dc.citation.number | 6 | - |
| dc.citation.startPage | 1764 | - |
| dc.citation.endPage | 1767 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Multidisciplinary | - |
| dc.subject.keywordPlus | C-H BOND | - |
| dc.subject.keywordPlus | ONE-POT SYNTHESIS | - |
| dc.subject.keywordPlus | ALKYNYL ETHERS | - |
| dc.subject.keywordPlus | ACID | - |
| dc.subject.keywordPlus | CYCLIZATION | - |
| dc.subject.keywordPlus | 6-SULFONYLINDOLES | - |
| dc.subject.keywordPlus | HYDROALKYLATION | - |
| dc.subject.keywordPlus | ISOMERIZATION | - |
| dc.subject.keywordPlus | REARRANGEMENT | - |
| dc.subject.keywordPlus | REACTIVITY | - |
| dc.subject.keywordAuthor | gold | - |
| dc.subject.keywordAuthor | homogeneous catalysis | - |
| dc.subject.keywordAuthor | hydroxylamines | - |
| dc.subject.keywordAuthor | nitrones | - |
| dc.subject.keywordAuthor | pyrrolidinones | - |
| dc.subject.keywordAuthor | redox chemistry | - |
| dc.identifier.url | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.201002863 | - |
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