Title: Lewis acid-base 1,2-addition reactions: synthesis of pyrylium borates from en-ynoate precursors
Citation
Wilkins LC, Hamilton HB, Kariuki BM, et al. (2017). Lewis acid-base 1,2-addition reactions: synthesis of pyrylium borates from en-ynoate precursors. Cardiff University. https://doi.org/10.17035/d.2017.0011648406
Access Rights: Creative Commons Attribution 4.0 International
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
Coverage start date: 01/06/2015
Coverage end date: 20/12/2016
Data format: .pdf, .cif
Software Required: Software to view NMR spectra e.g. MNova
Software to visualise X-ray structures e.g. Mercury
Avogadro software to visualise DFT calculations.
Estimated total storage size of dataset: Less than 100 megabytes
DOI : 10.17035/d.2017.0011648406
DOI URL: http://doi.org/10.17035/d.2017.0011648406
Treatment of methyl (Z)-2-alken-4-ynoates with the strong Lewis acid tris(pentafluorophenyl) borane, B(C6F5)3, yield substituted zwitterionic pyrylium borate species via an intramolecular 6-endo-dig cyclisation reaction. The supporting information, including figures of the NMR spectra for the compounds and reactions in the paper are included along with experimental procedures. X-ray data are included here which can be visualized using software for X-ray crystal structure determination/visualization which was used to characterise the compounds synthesised. Computation studies by DFT are included. Results based upon these data are published at http://doi.org/10.1039/c5dt03340c
Description
Keywords
Inspection with x-rays, structure-activity relationships, Structure elucidation, Synthesis
Related Projects
- CDT in Catalysis (22/10/2014 - 31/03/2015)