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and by FT-IR, making unnecessary any further blocking step.
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The quantitative disappearance of the hydroxyl groups in both the Merrifield-OH and the Wang resins can be followed by the Quiñoá test (Kuisle, O.; Quiñoá, E.; Riguera, R. Tetrahedron 1999, 55, 14807-14812) and by FT-IR, making unnecessary any further blocking step.
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We believe that such unexpected chlorination could have been achieved due to the traces of chlorine in the DCM, which under strong acid medium as the TFA and the presence of highly electron-rich aromatic rings facilitate this low yield secondary reaction. To the best of our knowledge, there are not precedents in the literature of this side-reaction
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We believe that such unexpected chlorination could have been achieved due to the traces of chlorine in the DCM, which under strong acid medium as the TFA and the presence of highly electron-rich aromatic rings facilitate this low yield secondary reaction. To the best of our knowledge, there are not precedents in the literature of this side-reaction
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Spectroscopic data was compared with the 2-methoxy-5-iodophenol synthesized by
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Spectroscopic data was compared with the 2-methoxy-5-iodophenol synthesized by Feldman K.S. J. Org. Chem. 62:1997;4983-4990
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Feldman, K.S.1
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C-H couplings) and NOESY (mixing time 600 ms) correlations were performed
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C-H couplings) and NOESY (mixing time 600 ms) correlations were performed
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Assignment may be reversed
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Assignment may be reversed
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