European Journal of Organic Chemistry p. 4840 - 4842 (2015)
Update date:2022-08-11
Topics:
Lim, Yi Wee
Hewitt, Russell J.
Burkett, Brendan A.
The rearrangement of substituted 1,4,2-oxathiazoles to nitriles in the presence of water is described. Preliminary investigations suggest that the reaction pathway proceeds via a 1,4,2-oxathiazolium intermediate, followed by trapping with water and subsequent decomposition to products. An unprecedented rearrangement of 5-phenyl-1,4,2-oxathiazoles bearing a C5 leaving group to nitriles in the presence of water is described.
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