
Journal of Organic Chemistry p. 3597 - 3599 (1993)
Update date:2022-08-11
Topics:
Janzen, Edward G.
Wilcox, Allan L.
Manoharan, Vinothane
By EPR, NMR, and TLC methods it was possible to show that nitric oxide (.NO) reacts with five different methyl- or tert-butyl-substituted phenols including α-tocopherol to produce the phenoxyl radical which subsequently couples reversibly with excess .NO.
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