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0000466076
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Synthesis of optically active α-amino acids
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Pergamon, Oxford
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U.S. Patent 4 084 953
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85030275449
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31P-NMR, IR and mass spectroscopy
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31P-NMR, IR and mass spectroscopy.
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85030273139
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note
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(14) A typical procedure is as follows: to a solution of freshly distilled THF (5ml) containing compound 1 (1eq, 0.66mmol), triphenylphosphine (2eq, 1.32mmol) and hydroxylamine (1.5eq, 0.99mmol), was added dropwise neat DEAD (2eq, 1.32mmol) under argon. The solution was stirred at room temperature until disappearance of the starting material (1-2 hours) and then concentrated in vacuo. The residue was purified by flash column chromatography over silica gel using a mixture of hexane-ethylacetate as eluant.
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0028019445
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(15) Gajda, T. Tetrahedron: Asymmetry 1994, 5, 1965-1972; Meier, C.; Laux, W.H.G.; Bats, J.W. Liebigs Ann. 1995, 1963-1979.
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0042898029
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(15) Gajda, T. Tetrahedron: Asymmetry 1994, 5, 1965-1972; Meier, C.; Laux, W.H.G.; Bats, J.W. Liebigs Ann. 1995, 1963-1979.
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Liebigs Ann.
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Meier, C.1
Laux, W.H.G.2
Bats, J.W.3
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