Direct preparation of [N,Cα]-diprotected L-α-aminoadipic acid from L-lysine
Abstract
L-Lysine was converted into N-benzyloxycarbonyl-L-α-aminoadipic acid 1-benzyl ester by a short route which avoids the intermediacy of L-α-aminoadipic acid.
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J. Chem. Soc., Chem. Commun., 1982, 818-819
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Direct preparation of [N,Cα]-diprotected L-α-aminoadipic acid from L-lysine
J. E. Baldwin, P. Harrison and J. A. Murphy, J. Chem. Soc., Chem. Commun., 1982, 818 DOI: 10.1039/C39820000818
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