Imperial College London
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Professor Philip J. Parsons

Faculty of Natural Sciences, Department of Chemistry

Senior Research Investigator
 
 
 
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Contact

 

p.parsons

 
 
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Location

 

110EMolecular Sciences Research HubWhite City Campus

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Summary

 

Publications

Citation

BibTex format

@article{Natho:2020:10.1016/j.tet.2020.131636,
author = {Natho, P and Annie, R and Greenfield, J and Allen, L and Andrew, W and Yang, T and Parsons, P},
doi = {10.1016/j.tet.2020.131636},
journal = {Tetrahedron},
title = {Regioselective synthesis of 1- and 4-tetralones from heteroaryl-3-cyclobutanols},
url = {http://dx.doi.org/10.1016/j.tet.2020.131636},
volume = {76},
year = {2020}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - Herein we describe the first transition-metal-free ring expansion of four-membered rings to 1-tetralones from 3-substituted heteroaromatic compounds, and the first example of an oxetanol ring expansion to an oxa-tetralone. We also experimentally investigate the mechanism of the silver-mediated ring expansion and elucidate the active oxidant in these systems using electrochemical techniques.
AU  - Natho,P
AU  - Annie,R
AU  - Greenfield,J
AU  - Allen,L
AU  - Andrew,W
AU  - Yang,T
AU  - Parsons,P
DO  - 10.1016/j.tet.2020.131636
PY  - 2020///
SN  - 0040-4020
TI  - Regioselective synthesis of 1- and 4-tetralones from heteroaryl-3-cyclobutanols
T2  - Tetrahedron
UR  - http://dx.doi.org/10.1016/j.tet.2020.131636
UR  - http://hdl.handle.net/10044/1/83846
VL  - 76
ER  -
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