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:2018:10.1021/acs.orglett.8b03619,
author = {Natho, P and Kapun, M and Allen, L and Parsons, PJ},
doi = {10.1021/acs.orglett.8b03619},
journal = {Organic Letters},
pages = {8030--8034},
title = {Regioselective transition-metal-free oxidative cyclobutanol ring expansion to 4-tetralones},
url = {http://dx.doi.org/10.1021/acs.orglett.8b03619},
volume = {20},
year = {2018}
}
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RIS format (EndNote, RefMan)

TY  - JOUR
AB  - A facile and transition-metal-free ring expansion of the cyclobutanol moiety to 4-tetralones fused to heteroaromatic systems is described. The oxidative ring expansion proceeds rapidly and regioselectively through mediation by N-bromosuccinimide and acetonitrile in satisfactory to good yields. The preparation of precursors, as well as the ring expansion have proven to be scalable and are straightforward to carry out
AU  - Natho,P
AU  - Kapun,M
AU  - Allen,L
AU  - Parsons,PJ
DO  - 10.1021/acs.orglett.8b03619
EP  - 8034
PY  - 2018///
SN  - 1523-7052
SP  - 8030
TI  - Regioselective transition-metal-free oxidative cyclobutanol ring expansion to 4-tetralones
T2  - Organic Letters
UR  - http://dx.doi.org/10.1021/acs.orglett.8b03619
UR  - http://hdl.handle.net/10044/1/66662
VL  - 20
ER  -
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