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o-Nitro- or o,p-dinitrophenylsulfonyl group has been reported to be eliminated under the milder reaction conditions: (a) Fukuyama, T.; Cheung, M.; Jow, C.-K.; Hidai, Y.; Kan, T. Tetrahedron Lett. 1997, 38, 5831-5834; (b) Hidai, Y.; Kan, T.; Fukuyama, T. Tetrahedron Lett. 1999, 40, 4711-4714.
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o-Nitro- or o,p-dinitrophenylsulfonyl group has been reported to be eliminated under the milder reaction conditions: (a) Fukuyama, T.; Cheung, M.; Jow, C.-K.; Hidai, Y.; Kan, T. Tetrahedron Lett. 1997, 38, 5831-5834; (b) Hidai, Y.; Kan, T.; Fukuyama, T. Tetrahedron Lett. 1999, 40, 4711-4714.
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Cenini et al. also reported nitrene transfer reaction using p-nitrophenyl azide as the nitrene source in the presence of metalloporphyrin, but high reaction temperature was required for the reaction: Cenini, S.; Tollari, S.; Penoni, A.; Cereda, C. J. Mol. Cat. A: Chem. 1999, 137, 135-146.
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