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The E/Z ratio was determined by comparison of the NMR spectroscopic data (olefinic proton, -NH, ester methyl group). This data is summarized in the Supporting Information. In most of the cases, the olefinic protons of (E)- 1 were observed at lower magnetic field than those of (Z)- 2. The tendency is consistent with the data reported by Mazurkiewicz et al., see.
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The E/Z ratio was determined by comparison of the NMR spectroscopic data (olefinic proton, -NH, ester methyl group). This data is summarized in the Supporting Information. In most of the cases, the olefinic protons of (E)- 1 were observed at lower magnetic field than those of (Z)- 2. The tendency is consistent with the data reported by Mazurkiewicz et al., see:, R. Mazurkiewicz, A. Kuźnik, M. Grymel, N. Kuźnik, Magn. Reson. Chem. 2005, 43, 36-40.
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This method has been successfully extended to the synthesis of phosphonoglycinate derivatives possessing an amino acid residue in the amino group. Full details and synthetic applications will be reported in due course
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This method has been successfully extended to the synthesis of phosphonoglycinate derivatives possessing an amino acid residue in the amino group. Full details and synthetic applications will be reported in due course.
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