25799-58-0Relevant articles and documents
Total Synthesis and Bioactivity Mapping of Geodiamolide H
Arndt, Hans-Dieter,B??neck, Johanna,Bellstedt, Peter,Dahse, Hans-Martin,G?rls, Helmar,Küllmer, Florian,Nasufovi?, Veselin,Stallforth, Pierre
, p. 11633 - 11642 (2021)
The first total synthesis of the actin-stabilizing marine natural product geodiamolide H was achieved. Solid-phase based peptide assembly paired with scalable stereoselective syntheses of polyketide building blocks and an optimized esterification set the
Synthesis of the polyketide section of seragamide A and related cyclodepsipeptides via Negishi cross coupling
Lang, Jan Hendrik,Lindel, Thomas
supporting information, p. 577 - 583 (2019/03/08)
The synthesis of the polyketide section present in the potently cytotoxic marine cyclodepsipeptide jasplakinolide and related natural products, geodiamolides and seragamides, is reported. The key step is a Negishi cross coupling of (R)-(3-methoxy-2-methyl
Total Synthesis of Geodiamolide A, a Novel Cyclodepsipeptide of Marine Origin
White, James D.,Amedio, John C.
, p. 736 - 738 (2007/10/02)
Geodiamolide A (1), a cyclodepsipeptide isolated from the sponge Geodia containing the new amino acid (R)-3-iodo-N-methyltyrosine, was synthesized from its constituent tripeptide and 8-hydroxynonenoic acid subunits.Final closure of the 18-membered ring wa
ROUTES TO THE TRIPEPTIDE UNIT OF GEODIAMOLIDE-A
Chiarello, Jack,Joullie, Madeleine M.
, p. 2211 - 2224 (2007/10/02)
Two different routes to the tripeptide unit of geodiamolide-A were investigated.