149357-30-2Relevant academic research and scientific papers
Total synthesis and cytotoxicity of the marine natural product malevamide D and a photoreactive analog
Telle, Werner,Kelter, Gerhard,Fiebig, Heinz-Herbert,Jones, Peter G.,Lindel, Thomas
supporting information, p. 316 - 322 (2014/03/21)
The marine natural product malevamide D from the cyanobacterium Symploca hydnoides was synthesized for the first time. The final peptide coupling linked the dolaisoleuine and dolaproine subunits. The phenyl group of malevamide D was also functionalized wi
A practical total synthesis of hapalosin, a 12-membered cyclic depsipeptide with multidrug resistance-reversing activity, by employing improved segment coupling and macrolactonization
Palomo, Claudio,Oiarbide, Mikel,Garcia, Jesus M.,Gonzalez, Alberto,Pazos, Raquel,Odriozola, Jose M.,Banuelos, Patricia,Tello, Monica,Linden, Anthony
, p. 4126 - 4134 (2007/10/03)
A practical total synthesis of hapalosin, a compound with multidrug resistance-reversing activity, has been carried out using an unprecedented macrolactonization strategy. One of the features of the new approach is the straightforward and fully stereocont
