156706-65-9Relevant academic research and scientific papers
An expeditious synthesis of geodiamolide a, an 18-membered cytotoxic depsipeptide from marine sponges
Shioiri, Takayuki,Imaed, Takayuki,Hamad, Yasumasa
, p. 421 - 442 (2007/10/03)
Geodiamolide A (1) has been efficiently synthesized from the polypropionate and tripeptide units using the Evans asymmetric alkylation, the Mitsunobu esterification, and the macrolactamization with diphenyl phosphorazidate (DPPA) as key steps. Efficient esterification between the complex polyketide and tripeptide units was also realized under high pressure conditions.
Efficient syntheses of geodiamolide A and jaspamide, cytotoxic and antifungal cyclic depsipeptides of marine sponge origin
Imaeda, Takayuki,Hamada, Yasumasa,Shioiri, Takayuki
, p. 591 - 594 (2007/10/02)
Geodiamolide A (1a) and jaspamide (2) have been efficiently synthesized by use of the Evans asymmetric alkylation, the Mitsunobu esterification, and the DPPA macrolactamization as key steps.
