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분자활성촉매반응연구단
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Regio- and Stereoselective Functionalization Enabled by Bidentate Directing Groups

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dc.contributor.authorJinwon Jeon-
dc.contributor.authorChangseok Lee-
dc.contributor.authorInyoung Park-
dc.contributor.authorSungwoo Hong-
dc.date.accessioned2022-01-05T02:30:07Z-
dc.date.available2022-01-05T02:30:07Z-
dc.date.created2021-07-07-
dc.date.issued2021-12-
dc.identifier.issn1527-8999-
dc.identifier.urihttps://pr.ibs.re.kr/handle/8788114/11010-
dc.description.abstract© 2021 The Chemical Society of Japan & Wiley-VCH GmbHChelation-assisted C−H bond and alkene functionalization using bidentate directing groups offers an elegant and versatile approach to overcome regiocontrol issues by allowing the catalyst to come into close proximity with the targeted sites. In this personal account, we highlight our recent works in developing regio- and stereocontrolled functionalizations through transition-metal catalysis enabled by bidentate directing groups. We classify our results into two categories: (1) regioselective alkene functionalization using bidentate directing groups, and (2) asymmetric C–H functionalization using chiral bidentate directing groups. Furthermore, density functional theory studies to elucidate the origin of the regio- and stereoselectivity exerted by bidentate directing groups are discussed.-
dc.language영어-
dc.publisherJohn Wiley and Sons Inc-
dc.titleRegio- and Stereoselective Functionalization Enabled by Bidentate Directing Groups-
dc.typeArticle-
dc.type.rimsART-
dc.identifier.wosid000657777100001-
dc.identifier.scopusid2-s2.0-85107200396-
dc.identifier.rimsid75976-
dc.contributor.affiliatedAuthorJinwon Jeon-
dc.contributor.affiliatedAuthorChangseok Lee-
dc.contributor.affiliatedAuthorInyoung Park-
dc.contributor.affiliatedAuthorSungwoo Hong-
dc.identifier.doi10.1002/tcr.202100117-
dc.identifier.bibliographicCitationChemical Record, v.21, no.12, pp.3613 - 3627-
dc.relation.isPartOfChemical Record-
dc.citation.titleChemical Record-
dc.citation.volume21-
dc.citation.number12-
dc.citation.startPage3613-
dc.citation.endPage3627-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.subject.keywordPlusALIPHATIC AMIDES-
dc.subject.keywordPlusCARBOXYLIC-ACIDS-
dc.subject.keywordPlusSULFINYL ANILINE-
dc.subject.keywordPlusAROMATIC AMIDES-
dc.subject.keywordPlusWACKER REACTION-
dc.subject.keywordPlusC-H BONDS-
dc.subject.keywordPlusCATALYZED DIRECT ARYLATION-
dc.subject.keywordPlusALKENYL CARBONYL-COMPOUNDS-
dc.subject.keywordPlusUNACTIVATED C(SP(3))-H BONDS-
dc.subject.keywordPlusREGIOSELECTIVE ARYLATION-
dc.subject.keywordAuthorbidentate directing group-
dc.subject.keywordAuthorchiral auxiliary-
dc.subject.keywordAuthorC−H functionalization-
dc.subject.keywordAuthorregioselectivity-
dc.subject.keywordAuthorstereoselectivity-
Appears in Collections:
Center for Catalytic Hydrocarbon Functionalizations(분자활성 촉매반응 연구단) > 1. Journal Papers (저널논문)
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