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https://doi.org/10.1039/c4cc04151h
| Title: | Allylic sp3 C-H borylation of alkenes via allyl-Pd intermediates: An efficient route to allylboronates | Authors: | Deng, H.-P Eriksson, L Szabó, K.J |
Keywords: | alcohol derivative aldehyde alkene allylboronate derivative benzaldehyde benzoquinone boronic acid derivative carbon glyceryl trinitrate hydrogen nitro benzaldehyde palladium tetramethyl benzoquinone unclassified drug allylation article borylation catalysis chemical reaction hydroboration oxidation synthesis |
Issue Date: | 2014 | Publisher: | Royal Society of Chemistry | Citation: | Deng, 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 | Rights: | Attribution 4.0 International | Abstract: | Palladium 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. | Source Title: | Chemical Communications | URI: | https://scholarbank.nus.edu.sg/handle/10635/180139 | ISSN: | 1359-7345 | DOI: | 10.1039/c4cc04151h | Rights: | Attribution 4.0 International |
| Appears in Collections: | Staff Publications Elements |
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