Cited 49 time in
Asymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of alpha-Quaternary Chiral beta-Lactams through Enantioselective C-H Insertion/Diastereoselective Allylation of Diazoamides
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Huang, Liang-Zhu | - |
| dc.contributor.author | Xuan, Zi | - |
| dc.contributor.author | Jeon, Hyun Ji | - |
| dc.contributor.author | Du, Zhen-Ting | - |
| dc.contributor.author | Kim, Ju Hyun | - |
| dc.contributor.author | Lee, Sang-gi | - |
| dc.date.accessioned | 2022-12-26T16:47:59Z | - |
| dc.date.available | 2022-12-26T16:47:59Z | - |
| dc.date.issued | 2018-08 | - |
| dc.identifier.issn | 2155-5435 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/11402 | - |
| dc.description.abstract | A straightforward route toward construction of a-quaternary chiral beta-lactam moiety via Rh(II)/Pd(0)-catalyzed stereoselective relay catalytic reaction is reported. This asymmetric dual relay catalysis involves Rh(II)-catalyzed enantioselective intramoluecular C-H insertions of alpha-diazoamides, and sequential Pd(0)-catalyzed diastereoselective intermolecular allylic alkylation. Under mild reaction conditions, a broad range of a-quaternary allylated chiral beta-lactams have been synthesized in high yields (up to 99%) with excellent stereoselectivities [up to diastereomeric ratio (dr) >99:1, up to 98% enantiomeric excess (ee)]. | - |
| dc.format.extent | 6 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | AMER CHEMICAL SOC | - |
| dc.title | Asymmetric Rh(II)/Pd(0) Relay Catalysis: Synthesis of alpha-Quaternary Chiral beta-Lactams through Enantioselective C-H Insertion/Diastereoselective Allylation of Diazoamides | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acscatal.8b01687 | - |
| dc.identifier.scopusid | 2-s2.0-85049316996 | - |
| dc.identifier.wosid | 000441112400053 | - |
| dc.identifier.bibliographicCitation | ACS CATALYSIS, v.8, no.8, pp 7340 - 7345 | - |
| dc.citation.title | ACS CATALYSIS | - |
| dc.citation.volume | 8 | - |
| dc.citation.number | 8 | - |
| dc.citation.startPage | 7340 | - |
| dc.citation.endPage | 7345 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Chemistry | - |
| dc.relation.journalWebOfScienceCategory | Chemistry, Physical | - |
| dc.subject.keywordPlus | INSERTION REACTIONS | - |
| dc.subject.keywordPlus | COOPERATIVE CATALYSIS | - |
| dc.subject.keywordPlus | KINUGASA REACTION | - |
| dc.subject.keywordPlus | AMINO ACIDS | - |
| dc.subject.keywordPlus | DIAZOACETAMIDES | - |
| dc.subject.keywordPlus | CONSTRUCTION | - |
| dc.subject.keywordPlus | ANNULATION | - |
| dc.subject.keywordPlus | KETENES | - |
| dc.subject.keywordPlus | ECONOMY | - |
| dc.subject.keywordPlus | PROGRESS | - |
| dc.subject.keywordAuthor | beta-lactam | - |
| dc.subject.keywordAuthor | rhodium | - |
| dc.subject.keywordAuthor | palladium | - |
| dc.subject.keywordAuthor | C-H insertion | - |
| dc.subject.keywordAuthor | allylic alkylation | - |
| dc.subject.keywordAuthor | asymmetric catalysis | - |
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