The Exploration of Aroyltrimethylgermane as Potent Synthetic Origins and Their Preparation

dc.bibliographicCitation.date2020
dc.bibliographicCitation.firstPage100771
dc.bibliographicCitation.issue1
dc.bibliographicCitation.journalTitleiScienceeng
dc.bibliographicCitation.volume23
dc.contributor.authorYuan, Yang
dc.contributor.authorZhang, Youcan
dc.contributor.authorChen, Bo
dc.contributor.authorWu, Xiao-Feng
dc.date.accessioned2022-12-08T07:12:00Z
dc.date.available2022-12-08T07:12:00Z
dc.date.issued2019
dc.description.abstractThe synthetic utilities of acylgermanes are surprisingly rarely explored compared with their analogues. In this communication, the survey of aroyltrimethylgermane as potent synthetic origins has been studied. A variety of novel chemical transformations have been realized, including using the acylgermane group as a directing group in Rh-catalyzed aromatic C-H alkenylation reaction and Ir-catalyzed aromatic C-H amidation reactions. Additionally, a general approach for acylgermanes preparation has been established as well. The catalytic system proceeds effectively in the presence of Pd(OAc)2/BINOL-based monophosphite (L11) and allows for the straightforward access to a wide range of functionalized acylgermanes in high yields. © 2019 The Author(s)Catalysis; Organic Synthesis; Organic Reaction; Chemical Synthesis © 2019 The Author(s)eng
dc.description.versionpublishedVersion
dc.identifier.urihttps://oa.tib.eu/renate/handle/123456789/10525
dc.identifier.urihttp://dx.doi.org/10.34657/9561
dc.language.isoeng
dc.publisherAmsterdam [u.a.] : Elsevier
dc.relation.doihttps://doi.org/10.1016/j.isci.2019.100771
dc.relation.essn2589-0042
dc.rights.licenseCC BY-NC-ND 4.0 Unported
dc.rights.urihttps://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.ddc050
dc.subject.otherCatalysiseng
dc.subject.otherChemical Synthesiseng
dc.subject.otherOrganic Reactioneng
dc.subject.otherOrganic Synthesiseng
dc.titleThe Exploration of Aroyltrimethylgermane as Potent Synthetic Origins and Their Preparationeng
dc.typeArticleeng
dc.typeTexteng
tib.accessRightsopenAccess
wgl.contributorLIKAT
wgl.subjectChemieger
wgl.typeZeitschriftenartikelger
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