Photochemical Rearrangement of 0-Phenyl-hydroxylamine

DOI QR Code

Synthesis Bungardner, C. L.;Lilly, R. L.
Synthesis Endo, Y.;Schudo, K.;Okamoto, T.
Synthesis Endo, Y.;Schudo, K.;Okamoto, T.
Tetrahedron Lett. v.27 Endo, Y.;Schudo, K.;Okamoto, T.
J. Amer. Chem. Soc. v.114 Haga, N.;Endo, Y.;Kataoka, K.;Yamaguchi, K.;Schudo, K.
Synthesis Krause, J. G.
J. Amer. Chem. Soc. v.96 Kalmus, C. E.;Hercules, D. M.
J. Amer. Chem. Soc. v.94 Meyer, J. W.;Hammond, G. S.
J. Org. Chem. v.52 Shine, H. J.;Subotkowski, W.
The products, phenol and aminophenols were identified by ¹H NMR, IR and Mass spectra comparing with those of authentic samples. Biphenyl and diphenylether derivatives were identified by comparison of GC retention times and Mass spectra with those of suthentic samples.