Total Synthesis of the Cyclic Depsipeptide Vioprolide D via its (Z)-Diastereoisomer
The first total synthesis of vioprolide D was accomplished in an overall yield of 2.0 % starting from methyl (2S)-3-benzyloxy-2-hydroxypropanoate (16 steps in the longest linear sequence). The cyclic depsipeptide was assembled from two building blocks of
Bach, Thorsten,Grab, Hanusch A.,Kirsch, Volker C.,Sieber, Stephan A.
supporting information
p. 12357 - 12361
(2020/05/05)
Total synthesis of the cytotoxic cyclopeptide mollamide, isolated from the sea squirt Didemnum molle
Full details of a total synthesis of the novel reverse prenyl substituted cyclic peptide mollamide, isolated from the ascidian Didemnum molle, are described.
McKeever, Benedict,Pattenden, Gerald
p. 2701 - 2712
(2007/10/03)
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