Title of article
Highly stereoselective and efficient synthesis of the dopa analogue in pepticinnamin E via enantioselective hydrogenation of dehydroamino acids
Author/Authors
SUN, Dequn Shandong University - Marine College, CHINA
From page
181
To page
186
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.
Keywords
Synthesis , dopa analogue , enantioselective hydrogenation , dehydroamino acid.
Journal title
Turkish Journal of Chemistry
Journal title
Turkish Journal of Chemistry
Record number
2533009
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