On the use of carboxamidomethyl esters (cam esters) in the synthesis of model peptides. scope and limitations
- 1 January 1985
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 41 (4) , 739-743
- https://doi.org/10.1016/s0040-4020(01)96451-8
Abstract
No abstract availableThis publication has 15 references indexed in Scilit:
- SYNTHESIS OF Nα-FORMYL-MET-LEU-PHE-OH: AN INDUCER OF CHEMOTAXIS IN PERITONEAL POLYMORPHONUCLEAR NEUTROPHILSInternational Journal of Peptide and Protein Research, 2009
- Carboxamidomethyl esters (CAM esters) as carboxyl protecting groups.Tetrahedron Letters, 1983
- Active Esters of Formic Acid as Useful Formylating Agents: Improvements in the Synthesis of Formyl-Amino Acid Esters, N-α-Formyl-Met-Leu-Phe-OH, and Formyl-Met-Lys-Pro-Arg, a Phagocytosis Stimulating PeptideSynthesis, 1982
- Side Reactions in Peptide SynthesisSynthesis, 1981
- Peptide Coupling Reagents VI1. A Novel, Cheaper Preparation of Benzotriazolyloxytris[dimethylamino]phosphonium Hexafluorophosphate (BOP Reagent)Synthesis, 1976
- 9-Fluorenylmethoxycarbonyl function, a new base-sensitive amino-protecting groupJournal of the American Chemical Society, 1970
- Simple route to sterically pure diketopiperazinesThe Journal of Organic Chemistry, 1968
- Glycolamide esters of N-acylamino acids and peptidesAustralian Journal of Chemistry, 1965
- t-Butyloxycarbonylamino Acids and Their Use in Peptide SynthesisJournal of the American Chemical Society, 1957
- New Amine-masking Groups for Peptide SynthesisJournal of the American Chemical Society, 1957