Teitl: Site Selective Csp3–Csp / Csp3–Csp2 Cross Coupling Reactions Using Frustrated Lewis Pairs: data
Dyfyniad
Dasgupta A, Stefkova K, Babaahmadi R, et al. (2021). Site Selective Csp3–Csp / Csp3–Csp2 Cross Coupling Reactions Using Frustrated Lewis Pairs: data. Cardiff University. https://doi.org/10.17035/d.2021.0130087985
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Dull Mynediad: I anfon cais i gael y data hwn, ebostiwch opendata@caerdydd.ac.uk
Crewyr y Set Ddata o Brifysgol Caerdydd
Manylion y Set Ddata
Cyhoeddwr: Cardiff University
Dyddiad (y flwyddyn) pryd y daeth y data ar gael i'r cyhoedd: 2021
Dyddiad dechrau creu'r data: 01.09.2019
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Amcangyfrif o gyfanswm maint storio'r set ddata: Llai na 100 megabeit
DOI : 10.17035/d.2021.0130087985
DOI URL: http://doi.org/10.17035/d.2021.0130087985
The donor-acceptor ability of frustrated Lewis pairs (FLPs) has led to widespread applications in organic synthesis. Single electron transfer from donor Lewis base to acceptor Lewis acid can generate the frustrated radical pair (FRP) depending on the substrate and energy required (thermal or photochemical) to promote an FLP into an FRP system. Herein, we report the Csp3–Csp cross coupling reaction of aryl esters with terminal alkynes using the B(C6F5)3/Mes3P FLP. Significantly, when the 1-ethynyl-4-vinylbenzene substrate was employed, exclusive formation of Csp3–Csp cross coupled products were observed. However, when 1-ethynyl-2-vinylbenzene was employed, solvent dependent site selective Csp3–Csp or Csp3–Csp2 cross coupling resulted. The nature of these reaction pathways and their selectivity has been investigated by extensive electron paramagnetic resonance (EPR) studies, kinetic studies, and density functional theory (DFT) calculations to elucidate both the mechanism of these coupling reactions as well as to explain the solvent dependent site selectivity. Data includes experimental procedures and characterisation data. Research results based upon these data are published at https://doi.org/10.1021/jacs.1c01622
Disgrifiad
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