Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (-)-pinolinone. Mayr, F., Wiegand, C., & Bach, T. Chemical Communications, 50(25):3353–3355, 2014. Publisher: The Royal Society of Chemistry![Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (-)-pinolinone [link]](https://bibbase.org/img/filetypes/link.svg "link")
Paper doi abstract bibtex The natural product (-)-pinolinone was synthesised via a concise route (six steps, 17% overall yield) from 3-acetoxyquinolone, employing an enantioselective intermolecular [2+2] photocycloaddition as the key step.
@article{mayr_enantioselective_2014,
title = {Enantioselective, intermolecular [2+2] photocycloaddition reactions of 3-acetoxyquinolone: total synthesis of (-)-pinolinone},
volume = {50},
issn = {1359-7345},
url = {http://dx.doi.org/10.1039/C3CC49469A},
doi = {10.1039/C3CC49469A},
abstract = {The natural product (-)-pinolinone was synthesised via a concise route (six steps, 17\% overall yield) from 3-acetoxyquinolone, employing an enantioselective intermolecular [2+2] photocycloaddition as the key step.},
number = {25},
journal = {Chemical Communications},
author = {Mayr, Florian and Wiegand, Christian and Bach, Thorsten},
year = {2014},
note = {Publisher: The Royal Society of Chemistry},
pages = {3353--3355},
}
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