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. http://doi.org/10.17035/d.2019.0084111418



Nid yw'r data hwn ar gael ar hyn o bryd oherwydd: Bwriad i gyhoeddi canlyniadau prosiect

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: 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/


Disgrifiad

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


Prosiectau Cysylltiedig

Diweddarwyd y tro diwethaf ar 2020-23-11 am 15:20