Title: Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles Using Alcohols


Citation
Dambatta MM, Polidano K (2019). Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles Using Alcohols. Cardiff University. http://doi.org/10.17035/d.2019.0072633299



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


Cardiff University Dataset Creators


Dataset Details

Publisher: Cardiff University

Date (year) of data becoming publicly available: 2019

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: 2518

DOI : 10.17035/d.2019.0072633299

DOI URL: http://doi.org/10.17035/d.2019.0072633299

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


Description

A general and efficient iron‐catalyzed C‐alkylation of oxindoles has been developed. This borrowing hydrogen approach employs a (cyclopentadienone)iron carbonyl complex (2 mol %) and exhibits a broad reaction scope, allowing benzylic and simple primary and secondary aliphatic alcohols to be employed as alkylating agents. A variety of oxindoles undergo selective mono‐C(3)‐alkylation in good to excellent isolated yields (28 examples, 50‐92% yield, 79% 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.

Research results based upon these data are puiblished at http://doi.org/10.1002/cssc.201900799


Research Areas

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Last updated on 2019-26-11 at 14:22