Title: B(C6F5)3-Catalyzed Direct C3 Alkylation of Indoles and Oxindoles - data


Citation
Basak S, Alvarez-Montoya A, Winfrey L, et al. (2020). B(C6F5)3-Catalyzed Direct C3 Alkylation of Indoles and Oxindoles - data. Cardiff University. https://doi.org/10.17035/d.2020.0104936560



Access Rights: Data is provided under a Creative Commons Attribution (CC BY 4.0) licence

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: 2020

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: 5298

DOI : 10.17035/d.2020.0104936560

DOI URL: http://doi.org/10.17035/d.2020.0104936560

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


Description

The direct C3 alkylation of indoles and oxindoles is a challenging transformation and only a few direct methods exist. Utilizing the underexplored ability of triaryl boranes to mediate the heterolytic cleavage of α-nitrogen C–H bonds in amines, we have developed a catalytic approach for the direct C3 alkylation of a wide range of indoles and oxindoles using amine based alkylating agents. We also employed this borane-catalyzed strategy in an alkylation-ring opening cascade.

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.


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Last updated on 2022-29-04 at 14:42