Teitl: Exploring tandem ruthenium-catalyzed hydrogen transfer and SNAr chemistry

Dyfyniad
Polidano K, Reed-Berendt BG, Basset A, et al. (2017). Exploring tandem ruthenium-catalyzed hydrogen transfer and SNAr chemistry. Cardiff University. https://doi.org/10.17035/d.2017.0044059416

Manylion y Set Ddata

Cyhoeddwr: Cardiff University

Dyddiad (y flwyddyn) pryd y daeth y data ar gael i'r cyhoedd: 2017

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: 4666

DOI : 10.17035/d.2017.0044059416

DOI URL: http://doi.org/10.17035/d.2017.0044059416

Related URL: http://blogs.cardiff.ac.uk/themorrillgroup/

Disgrifiad

A hydrogen transfer strategy for the catalytic functionalization of benzylic alcohols via electronic arene activation, accessing a diverse range of bespoke diaryl ethers and aryl amines in excellent isolated yields (38 examples, 70% average yield) has been explored. Taking advantage of the hydrogen transfer approach, the oxidation level of the functionalized products can be selected by judicious choice of simple and inexpensive additives.

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://dx.doi.org/10.1021/acs.orglett.7b03441