•  
  •  
 

Turkish Journal of Chemistry

Authors

DEQUN SUN

DOI

10.3906/kim-0904-14

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.

First Page

181

Last Page

186

Included in

Chemistry Commons

Share

COinS