Highly stereoselective and efficient synthesis of the dopa analogue in pepticinnamin E via enantioselective hydrogenation of dehydroamino acids

Authors : Highly stereoselective and efficient syn In

Pages : 181-186

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Publication Date : 0000-00-00

Article Type : Research Paper

Abstract :An efficient and new method was developed to prepare the dopa analogue 11 in natural pepticinnamin via catalytic hydrogenation of dehydroamino acids insert ignore into journalissuearticles values(DDAA); with a good yield and ee. Product 11 is a key intermediate towards the total synthesis of pepticinnamin E and its analogues.
Keywords : Synthesis, dopa analogue, enantioselective hydrogenation, dehydroamino acid