Routes to the Tripeptide Unit of Geodiamoude-A
- 1 December 1988
- journal article
- research article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 18 (18) , 2211-2223
- https://doi.org/10.1080/00397918808082363
Abstract
Two different routes to the tripeptide unit of geodiamolide-A were investigated.Keywords
This publication has 10 references indexed in Scilit:
- Convergent, enantiospecific total synthesis of the novel cyclodepsipeptide (+)-jasplakinolide (jaspamide)Journal of the American Chemical Society, 1988
- Total syntheses of jaspamide (jasplakinolide) and geodiamolide A and B - 1. Stereoselective synthesis of (2,4,6,8)-8-hydroxy-2,4,6-trimethyl-4-nonenoicic acid1Tetrahedron Letters, 1988
- Synthetic studies of didemnins. II. Approaches to statine diastereomersTetrahedron Letters, 1987
- Immonium ion based synthetic methodology: a novel method for the N-methylation of dipeptides and amino acid derivatives via retro aza Diels-Alder reactionsThe Journal of Organic Chemistry, 1987
- Stereostructures of geodiamolides A and B, novel cyclodepsipeptides from the marine sponge Geodia spThe Journal of Organic Chemistry, 1987
- N,N'‐bis(2‐oxo‐3‐oxazolidinyl) phosphinic chloride (BOP‐Cl); a superb reagent for coupling at and with iminoacid residuesInternational Journal of Peptide and Protein Research, 1987
- Jaspamide, a modified peptide from a Jaspis sponge, with insecticidal and antifungal activityJournal of the American Chemical Society, 1986
- Jasplakinolide, a cyclodepsipeptide from the marine sponge, SP.Tetrahedron Letters, 1986
- Synthesis of 9-fluorenylmethyloxycarbonyl-protected N-alkyl amino acids by reduction of oxazolidinonesThe Journal of Organic Chemistry, 1983
- N-Methylamino acids in peptide synthesis. V. The synthesis of N-tert-butyloxycarbonyl, N-methylamino acids by N-methylationCanadian Journal of Chemistry, 1977