@article{31b2d2e50cb6423985a7759980bef9e0,
title = "Deprotonation of Benzoxazolium Salt: Trapping of a Radical-Cation Intermediate",
abstract = " The deprotonation of N-2,6-diisopropylphenyl-substituted benzoxazolium tetrafluoroborate 1 with NaH results in the formation of electron-rich diaminodioxaethylene 2. The radical cation salt 2 ·+ ·BF 4 - is found to be an intermediate product in the redox reaction leading from 1 to 2. ",
keywords = "N-HETEROCYCLIC CARBENES, TRANSITION-METAL-COMPLEXES, COORDINATION CHEMISTRY, IMIDAZOLIUM SALTS, LIGANDS, REACTIVITY, PRECURSORS, ISOCYANIDE, OXIDATION, CATALYSTS",
author = "Klementyeva, {Svetlana V.} and Abramov, {Pavel A.} and Somov, {Nikolay V.} and Dudkina, {Yulia B.} and Budnikova, {Yulia H.} and Poddel'Sky, {Andrey I.}",
year = "2019",
month = feb,
day = "15",
doi = "10.1021/acs.orglett.8b03928",
language = "English",
volume = "21",
pages = "946--950",
journal = "Organic Letters",
issn = "1523-7060",
publisher = "American Chemical Society",
number = "4",
}