Teitl: One-pot conversion of allylic alcohols to a-methyl ketones via iron-catalyzed isomerization-methylation
Dyfyniad
Latham DE, Polidano K, Morrill LC (2019). One-pot conversion of allylic alcohols to a-methyl ketones via iron-catalyzed isomerization-methylation. Cardiff University. https://doi.org/10.17035/d.2019.0084111418
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Hawliau Mynediad: Darperir Data dan drwydded Creative Commons Attribution (CC BY 4.0)
Dull Mynediad: I anfon cais i gael y data hwn, ebostiwch opendata@caerdydd.ac.uk
Manylion y Set Ddata
Cyhoeddwr: Cardiff University
Dyddiad (y flwyddyn) pryd y daeth y data ar gael i'r cyhoedd: 2019
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
Nifer y ffeiliau yn y set ddata: 3756
DOI : 10.17035/d.2019.0084111418
DOI URL: http://doi.org/10.17035/d.2019.0084111418
Related URL: http://blogs.cardiff.ac.uk/themorrillgroup/
A one-pot iron-catalyzed conversion of allylic alcohols to a-methyl ketones has been developed. This isomerization-methylation strategy utilized a (cyclopentadienone)iron(0) carbonyl complex as precatalyst and methanol as the C1 source. A diverse range of allylic alcohols undergo isomerization-methylation to form a-methyl ketones in good isolated yields (up to 84% isolated 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 spectrometry spectra Research results based upon these data are published at http://doi.org/10.1021/acs.orglett.9b02900
Disgrifiad
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