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7
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0000564117
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A series of related hydrophobic 2-(thioalkyl)ethyl carbamates have also been generated via primary amine addition to an appropriately activated carbonate, which provides an elegant capping method for the chromatographic purification of peptides
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A series of related hydrophobic 2-(thioalkyl)ethyl carbamates have also been generated via primary amine addition to an appropriately activated carbonate, which provides an elegant capping method for the chromatographic purification of peptides. (García-Echeverría, C. J. Chem. Soc., Chem. Commun. 1995, 779-780).
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García-Echeverría, C.1
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37049080767
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A related ester linkage has also been described
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A related ester linkage has also been described (Katti, S. B.; Misra, P. K.; Haq, W.; Mathur, K. B. J. Chem. Soc., Chem. Commun. 1992, 843-844).
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0343028796
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11-13 and this may offer possible synthetic advantage over the oxidation/base-mediated elimination protocol under appropriate circumstances
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11-13 and this may offer possible synthetic advantage over the oxidation/base-mediated elimination protocol under appropriate circumstances.
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14
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0343028795
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Iwasaki, T.; Miyoshi, M.; Matsuoka, M.; Matsumoto, K. Chem. Ind. 1973, 1163-1164.
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0018479645
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note
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4OH in 2,2,2-trifluoroethanol as the reagent for achieving cleavage of the resin-bound sulfone, although no chemical yields were actually reported. Using his conditions, we only observed a 24% yield of piperazine 6, as compared to 47% using the modified procedure.
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0033548667
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For a recent report describing the use of a triazine linker that is applicable to amino ketones
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For a recent report describing the use of a triazine linker that is applicable to amino ketones, see: Bräse, S.; Köbberling, J.; Enders, D.; Lazny, R.; Wang, M.; Brandtner, S. Tetrahedron Lett. 1999, 40, 2105-2108.
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