Turkish Journal of Chemistry
Abstract
An efficient and new method was developed to prepare the dopa analogue 11 in natural pepticinnamin via catalytic hydrogenation of dehydroamino acids (DDAA) with a good yield and ee. Product 11 is a key intermediate towards the total synthesis of pepticinnamin E and its analogues.
DOI
10.3906/kim-0904-14
Keywords
Synthesis; dopa analogue; enantioselective hydrogenation; dehydroamino acid.
First Page
181
Last Page
186
Recommended Citation
SUN, D (2010). Highly stereoselective and efficient synthesis of the dopa analogue in pepticinnamin E via enantioselective hydrogenation of dehydroamino acids. Turkish Journal of Chemistry 34 (2): 181-186. https://doi.org/10.3906/kim-0904-14
