Teitl: Transition Metal Free alpha-C-Alkylation of Ketones Using Secondary Alcohols - data
Dyfyniad
Dambatta M (2020). Transition Metal Free alpha-C-Alkylation of Ketones Using Secondary Alcohols - data. Cardiff University. https://doi.org/10.17035/d.2020.0116098795
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Dull Mynediad: Bydd https://doi.org/10.17035/d.2020.0116098795 yn mynd â chi i dudalen storio ar gyfer y set ddata hon, lle byddwch chi’n gallu lawrlwytho'r data neu ddod o hyd i ragor o wybodaeth mynediad, fel y bo'n briodol.
Manylion y Set Ddata
Cyhoeddwr: Cardiff University
Dyddiad (y flwyddyn) pryd y daeth y data ar gael i'r cyhoedd: 2020
Fformat y data: .txt, .inmr, .info, .par, .xml, .pdf, .temp, .back, .jpg, .ispd
Meddalwedd ofynnol: An appropriate NMR processing software is required for raw NMR data files
Amcangyfrif o gyfanswm maint storio'r set ddata: Llai nag 1 gigabeit
DOI : 10.17035/d.2020.0116098795
DOI URL: http://doi.org/10.17035/d.2020.0116098795
Related URL: http://blogs.cardiff.ac.uk/themorrillgroup/
A base-mediated a-C-alkylation of ketones with secondary alcohols has been developed. This transition metal free approach employs KOt-Bu as the base and exhibits a broad scope, allowing a range of commodity aliphatic secondary alcohols and 1-arylethanols to be employed as alkylating agents. Aryl methyl ketones undergo selective mono-a-C-alkylation in high isolated yields (23 examples, 65% average yield). Analysis of reaction products from this methodology resulted in the following data: 1H, 19F and 13C NMR raw data files IR spectra High-Resolution Mass Spectrography spectra.
Disgrifiad
Prosiectau Cysylltiedig
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