Design on an affinity-based Nα-amino protecting group for peptide synthesis: tetrabenzo[a,c,g,i]fluorenyl-17-methyl urethanes (Tbfmoc)
- 14 January 1992
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 33 (3) , 385-388
- https://doi.org/10.1016/s0040-4039(00)74138-4
Abstract
No abstract availableKeywords
This publication has 14 references indexed in Scilit:
- On-resin biotinylation of chemically synthesized proteins for one-step purificationAnalytical Biochemistry, 1988
- High-performance immobilized metal ion affinity chromatography of peptides: Analytical separation of biologically active synthetic peptidesAnalytical Biochemistry, 1988
- Structure and performance of porous graphitic carbon in liquid chromatographyJournal of Chromatography A, 1986
- Purification of a synthetic peptide with the aid of covalent chromatographyJournal of Chromatography A, 1978
- Affinity purification of synthetic peptides.Proceedings of the National Academy of Sciences, 1976
- Metal chelate affinity chromatography, a new approach to protein fractionationNature, 1975
- Affinity Chromatography. New Approaches for the Preparation of Spacer Containing Derivatives and for Specific Isolation of PeptidesPublished by Springer Nature ,1974
- 9-Fluorenylmethoxycarbonyl amino-protecting groupThe Journal of Organic Chemistry, 1972
- Sepharose-avidin column for the binding of biotin or biotin-containing peptidesCellular and Molecular Life Sciences, 1970
- Studies on Polypeptides. XXXV. Synthesis of S-Peptide1-20 and Its Ability to Activate S-Protein1-3Journal of the American Chemical Society, 1966