A comparison of acid labile linkage agents for the synthesis of peptide C-terminal amides
- 31 December 1989
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 30 (35), 4645-4648
- https://doi.org/10.1016/s0040-4039(01)80764-4
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- A modified benzhydrylamine as a handle reagent for the solid phase synthesis of peptide amides based on the fluorenylmethoxycarbonyl methodJournal of the Chemical Society, Chemical Communications, 1988
- Preparation and application of new acid labile anchor groups for the synthesis of peptide amides by FMOC solid phase synthesisTetrahedron Letters, 1987
- An acid‐labile anchoring linkage for solid‐phase synthesis of C‐terminal peptide amides under mild conditions*International Journal of Peptide and Protein Research, 1987
- Solid-phase synthesis of peptide amides on a polystyrene support using fluorenylmethoxycarbonyl protecting groupsThe Journal of Organic Chemistry, 1987
- Solid-phase synthesis of protected peptide fragments using a trialkoxy-diphenyl-methylester resin.Tetrahedron Letters, 1987
- Synthesis of N‐tert.‐butoxycarbonyl(α‐phenyl)aminomethylphenoxyacetic acid for use as a handle in solid‐phase synthesis of peptide α‐carboxamidesInternational Journal of Peptide and Protein Research, 1981
- 9-Fluorenylmethoxycarbonyl function, a new base-sensitive amino-protecting groupJournal of the American Chemical Society, 1970