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


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



Access Rights: Data can be made freely available subject to attribution

Access Method: Click to email a request for this data to opendata@cardiff.ac.uk


Dataset Details

Publisher: Cardiff University

Date (year) of data becoming publicly available: 2017

Data format: .txt, .inmr, .info, .par, .xml, .pdf, .temp, .back, .jpg, .ispd

Software Required: An appropriate NMR processing software is required for raw NMR data files

Estimated total storage size of dataset: Less than 1 gigabyte

Number of Files In Dataset: 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/


Description

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


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Last updated on 2019-23-07 at 11:01