An efficient process for the synthesis of (R)-N-t-Boc-4-piperidinylglycine
8a, an unnatural amino acid, via enantioselective rhodium-catalyzed hydroge
nation of the Cbz-enamide 5a is described. Subsequent deprotection of 8a af
fords unprotected (R)-4-piperidinylglycine 9 in good yield. (C) 2001 Elsevi
er Science Ltd. All rights reserved.