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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c4cc04151h
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dc.titleAllylic sp3 C-H borylation of alkenes via allyl-Pd intermediates: An efficient route to allylboronates
dc.contributor.authorDeng, H.-P
dc.contributor.authorEriksson, L
dc.contributor.authorSzabó, K.J
dc.date.accessioned2020-10-26T07:11:09Z
dc.date.available2020-10-26T07:11:09Z
dc.date.issued2014
dc.identifier.citationDeng, H.-P, Eriksson, L, Szabó, K.J (2014). Allylic sp3 C-H borylation of alkenes via allyl-Pd intermediates: An efficient route to allylboronates. Chemical Communications 50 (65) : 9207-9210. ScholarBank@NUS Repository. https://doi.org/10.1039/c4cc04151h
dc.identifier.issn1359-7345
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/180139
dc.description.abstractPalladium catalyzed allylic C-H functionalization was performed using exocyclic alkene substrates. Multi-component synthesis of stereodefined homoallylic alcohols could be performed using a reaction sequence involving allylic C-H borylation and allylation of aldehydes. This journal is © the Partner Organisations 2014.
dc.publisherRoyal Society of Chemistry
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectalcohol derivative
dc.subjectaldehyde
dc.subjectalkene
dc.subjectallylboronate derivative
dc.subjectbenzaldehyde
dc.subjectbenzoquinone
dc.subjectboronic acid derivative
dc.subjectcarbon
dc.subjectglyceryl trinitrate
dc.subjecthydrogen
dc.subjectnitro benzaldehyde
dc.subjectpalladium
dc.subjecttetramethyl benzoquinone
dc.subjectunclassified drug
dc.subjectallylation
dc.subjectarticle
dc.subjectborylation
dc.subjectcatalysis
dc.subjectchemical reaction
dc.subjecthydroboration
dc.subjectoxidation
dc.subjectsynthesis
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c4cc04151h
dc.description.sourcetitleChemical Communications
dc.description.volume50
dc.description.issue65
dc.description.page9207-9210
dc.published.statePublished
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