289622-52-2Relevant academic research and scientific papers
Stereochemistry and total synthesis of janolusimide, a tripeptide marine toxin
Giordano, Assunta,Della Monica, Carmela,Landi, Francesco,Spinella, Aldo,Sodano, Guido
, p. 3979 - 3982 (2000)
The stereochemistry of janolusimide, a lipophilic tripeptide marine toxin, has been fully elucidated by stereoselective synthesis of the lactam component (5S)-3,3'-dimethyl-5-isopropylpyrrolidin-2,4-dione. The peptide was then synthesized in 13 steps and in 0.8% total yield. (C) 2000 Elsevier Science Ltd.
