Electrosynthesis of nitroso compounds from (1S, 2S)-2-amino-l-(4-nitrophenyl)-propane-1,3-diol derivatives
Nitroso compounds were electrogenerated from (1S, 2S)-2-amino-1-(4-nitrophenyl)-propane-1,3-diol derivatives (derivatives of p-nitrophenylserinol) in a 'redox' flow cell equipped with two consecutive porous electrodes of opposite polarities. In spite. of the relative instability in methano...
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Veröffentlicht in: | Journal of applied electrochemistry 2005-09, Vol.35 (9), p.851-855 |
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container_title | Journal of applied electrochemistry |
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creator | Cristea, C. V. Moinet, C. Jitaru, M. Popescu, I. C. |
description | Nitroso compounds were electrogenerated from (1S, 2S)-2-amino-1-(4-nitrophenyl)-propane-1,3-diol derivatives (derivatives of p-nitrophenylserinol) in a 'redox' flow cell equipped with two consecutive porous electrodes of opposite polarities. In spite. of the relative instability in methanol-acetate buffer of the hydroxylamine intermediates produced at the first porous electrode (cathode), the nitroso derivatives were prepared in good yields at the second one (anode). A coupling reaction between some nitroso derivatives and p-toluenesulphinic acid led to N-sulphonylphenylhydroxylamines. |
doi_str_mv | 10.1007/s10800-005-1320-9 |
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title | Electrosynthesis of nitroso compounds from (1S, 2S)-2-amino-l-(4-nitrophenyl)-propane-1,3-diol derivatives |
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