Synthesis of 2,3- and 3,4-methanoamino acid equivalents with stereochemical diversity and their conversion into the tripeptide proteasome inhibitor belactosin a and its highly potent cis-cyclopropane stereoisomer.
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S. Shuto | A. Matsuda | H. Yokosawa | A. Asai | K. Yamaguchi | Keisuke Yoshida | Y. Unno | T. Sone | M. Arisawa