Efficient syntheses of geodiamolide A and jaspamide, cytotoxic and antifungal cyclic depsipeptides of marine sponge origin
- 31 December 1994
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 35 (4), 591-594
- https://doi.org/10.1016/s0040-4039(00)75846-1
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Asymmetric total synthesis of (+)-jasplakinolideThe Journal of Organic Chemistry, 1991
- Self-reproduction of chirality. Asymmetric synthesis of .beta.-aryl-.beta.-amino acids from enantiomerically pure dihydropyrimidinonesThe Journal of Organic Chemistry, 1991
- A Total Synthesis of (+)-Geodiamolides A and B, the Novel CyclodesiprptidesHETEROCYCLES, 1990
- Total synthesis of geodiamolide A, a novel cyclodepsipeptide of marine originThe Journal of Organic Chemistry, 1989
- A Total Synthesis of the Novel Cyclodepsipeptide (+)-Geodiamolide AHETEROCYCLES, 1989
- Routes to the Tripeptide Unit of Geodiamoude-ASynthetic Communications, 1988
- Convergent, enantiospecific total synthesis of the novel cyclodepsipeptide (+)-jasplakinolide (jaspamide)Journal of the American Chemical Society, 1988
- Stereostructures of geodiamolides A and B, novel cyclodepsipeptides from the marine sponge Geodia spThe Journal of Organic Chemistry, 1987
- Jaspamide, a modified peptide from a Jaspis sponge, with insecticidal and antifungal activityJournal of the American Chemical Society, 1986
- N-Methylamino Acids in Peptide Synthesis. II. A New Synthesis of N-Benzyloxycarbonyl, N-Methylamino AcidsCanadian Journal of Chemistry, 1973