Total Synthesis of the Nematicidal Cyclododecapeptide Omphalotin A by Using Racemization-Free Triphosgene-Mediated Couplings in the Solid Phase
- 3 July 2002
- journal article
- research article
- Published by Wiley in Angewandte Chemie International Edition in English
- Vol. 41 (13) , 2307-2309
- https://doi.org/10.1002/1521-3773(20020703)41:13<2307::aid-anie2307>3.0.co;2-y
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Triphosgene as highly efficient reagent for the solid-phase coupling of N-alkylated amino acids—total synthesis of cyclosporin OTetrahedron Letters, 2002
- A novel thiazolium type peptide coupling reagent for hindered amino acidsTetrahedron Letters, 1999
- In situ generation of Fmoc‐amino acid chlorides using bis‐(trichloromethyl)carbonate and its utilization for difficult couplings in solid‐phase peptide synthesisChemical Biology & Drug Design, 1999
- Solid-Phase Total Synthesis of Cyclosporine AnaloguesHelvetica Chimica Acta, 1997
- Omphalotin, A New Cyclic Peptide with Potent Nematicidal Activity fromOmphalotus OleariusII. Isolation and Structure DeterminationNatural Product Letters, 1997
- Omphalotin, A New Cyclic Peptide with Potent Nematicidal Activity fromOmphalotus OleariusI. Fermentation and Biological ActivityNatural Product Letters, 1997
- Lability of N‐alkylated peptides towards TFA cleavageInternational Journal of Peptide and Protein Research, 1996
- A new reagent for the cleavage of fully protected peptides synthesised on 2-chlorotrityl chloride resinJournal of the Chemical Society, Chemical Communications, 1994
- Synthesis of 9-fluorenylmethyloxycarbonyl-protected N-alkyl amino acids by reduction of oxazolidinonesThe Journal of Organic Chemistry, 1983
- N-Methylamino Acids in Peptide Synthesis. III. Racemization during Deprotection by Saponification and AcidolysisCanadian Journal of Chemistry, 1973