Convergent solid phase peptide synthesis vi : synthesis by the fmoc procedure with a modified protocol of two protected segments, sequence 5-17 and 18-31 of the neurotoxin ii of the scorpion androctonus australis hector.
- 1 January 1987
- journal article
- research article
- Published by Elsevier in Tetrahedron
- Vol. 43 (24), 5973-5980
- https://doi.org/10.1016/s0040-4020(01)87803-0
Abstract
No abstract availableThis publication has 20 references indexed in Scilit:
- Convergent solid phase peptide synthesis-IIITetrahedron, 1986
- Convergent solid phase peptide synthesis IV.Tetrahedron, 1986
- Formation of oligopeptides during the synthesis of 9‐fluorenylmethyloxycarbonyl amino acid derivativesBiopolymers, 1983
- Amino‐acids condensations in the preparation of Nα‐9‐fluorenylrnethyloxycarbonylamino‐acids with 9‐fluorenylmethylchloroformateInternational Journal of Peptide and Protein Research, 1983
- Synthesis ofN-2,2,2-(Trichloroethoxycarbonyl)-L-amino Acids andN-(9-Fluorenylmethoxycarbonyl)-L-amino Acids Involving Succinimidoxy Anion as a Leaving Group in Amino Acid ProtectionSynthesis, 1983
- Introduction of 9-fluorenylmethyloxycarbonyl, trichloroethoxycarbonyl, and benzyloxycarbonyl amine protecting groups into O-unprotected hydroxyamino acids using succinimidyl carbonatesCanadian Journal of Chemistry, 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
- Easily prepared polar support for solid phase peptide and oligonucleotide synthesis. Preparation of substance P and a nonadeoxyribonucleotideJournal of the Chemical Society, Chemical Communications, 1979
- A new amino protecting group removable by reduction. Chemistry of the dithiasuccinoyl (Dts) functionJournal of the American Chemical Society, 1977