Asymmetric C-H Functionalization of Cyclopropanes Using an Isoleucine-NH2 Bidentate Directing Group
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jinhee Kim | - |
dc.contributor.author | Mikyung Sim | - |
dc.contributor.author | Namhoon Kim | - |
dc.contributor.author | Sungwoo Hong | - |
dc.date.available | 2018-07-18T02:09:50Z | - |
dc.date.created | 2018-03-15 | - |
dc.date.issued | 2015-10 | - |
dc.identifier.issn | 0039-7881 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/4851 | - |
dc.description.abstract | The systematic investigation of substrate-bound a-amino acid auxiliaries has resulted in catalytic asymmetric C–H functionalization of cyclopropanes enabled by amino acid amides as chiral bidentate directing groups. The use of an Ile-NH2 auxiliary embedded in the substrate provided excellent levels of asymmetric induction (diastereomeric ratio of up to 72 : 1) in the Pd(II)-catalyzed b-methylene C(sp3)–H bond activation of cyclopropanes and cross-coupling with aryl iodides. This journal is © The Royal Society of Chemistry 2015 | - |
dc.language | 영어 | - |
dc.publisher | GEORG THIEME VERLAG KG | - |
dc.title | Asymmetric C-H Functionalization of Cyclopropanes Using an Isoleucine-NH2 Bidentate Directing Group | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000362568400001 | - |
dc.identifier.scopusid | 2-s2.0-84943278596 | - |
dc.identifier.rimsid | 62542 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Jinhee Kim | - |
dc.contributor.affiliatedAuthor | Mikyung Sim | - |
dc.contributor.affiliatedAuthor | Namhoon Kim | - |
dc.contributor.affiliatedAuthor | Sungwoo Hong | - |
dc.identifier.doi | 10.1055/s-0035-1560166 | - |
dc.identifier.bibliographicCitation | SYNTHESIS-STUTTGART, v.47, no.19, pp.A136 - A139 | - |
dc.relation.isPartOf | SYNTHESIS-STUTTGART | - |
dc.citation.title | SYNTHESIS-STUTTGART | - |
dc.citation.volume | 47 | - |
dc.citation.number | 19 | - |
dc.citation.startPage | A136 | - |
dc.citation.endPage | A139 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.scptc | 40 | - |
dc.description.journalClass | 1 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalWebOfScienceCategory | Chemistry, Organic | - |