Peptide synthesis by a combination of solid-phase and solution methods I: A new very acid-labile anchor group for the solid phase synthesis of fully protected fragments
Authors:
- 31 December 1988
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 29 (32) , 4005-4008
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- Anwendung von d-Chirasil-Val bei der gas-chromatographischen Analytik von EnantiomerenAnalytical and Bioanalytical Chemistry, 1985
- A new base-catalyzed cleavage reaction for the preparation of protected peptidesTetrahedron, 1984
- Acid‐labile resin linkage agents for use in solid phase peptide synthesisInternational Journal of Peptide and Protein Research, 1982
- Convergent solid phase peptide synthesis. II. Synthesis of the 1–6 apamin protected segment on a NBB-resin. Synthesis of apaminTetrahedron, 1982
- Convergent solid phase peptide synthesis. I. Synthesis of protected segments on a hydroxymethylphenyloxymethyl resin using the base labile FMOC α-amine protection. Model synthesis of LHRH.Tetrahedron, 1982
- A new protecting group combination for solid phase synthesis of protected peptidesJournal of the Chemical Society, Chemical Communications, 1982
- A rapid non-acidolytic method for deprotection and removal of peptides from solid phase resins - applications of ammonium formate catalytic transfer hydrogenationTetrahedron Letters, 1981
- Improved synthesis of 4-alkoxybenzyl alcohol resinThe Journal of Organic Chemistry, 1981
- Rapid Gas Chromatographic Separation of Amino Acid Enantiomers with a Novel Chiral Stationary PhaseJournal of Chromatographic Science, 1977
- Solid Phase Peptide Synthesis employing Haloacylpolystyrene as a Polymer SupportChemical and Pharmaceutical Bulletin, 1970