Use of 2,2′-dithiobis(5-nitropyridine) for the heterodimerization of cysteine containing peptides. Introduction of the 5-nitro-2-pyridinesulfenyl group
Open Access
- 26 February 1996
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 37 (9) , 1347-1350
- https://doi.org/10.1016/0040-4039(96)00019-6
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Synthesis of disulfide‐bridged fragments of ω‐conotoxins GVIA and MVIIAInternational Journal of Peptide and Protein Research, 1994
- Total synthesis of human insulin by regioselective disulfide formation using the silyl chloride-sulfoxide methodJournal of the American Chemical Society, 1993
- Preparation and application of the 5-(4-(9-fluorenylmethyloxycarbonyl)aminomethyl-3,5-dimethoxyphenoxy)-valeric acid (PAL) handle for the solid-phase synthesis of C-terminal peptide amides under mild conditionsThe Journal of Organic Chemistry, 1990
- Solid-phase-mediated peptide heterodisulfide formationJournal of the American Chemical Society, 1990
- Uteroglobin-like peptide cavities I. Synthesis of antiparallel and parallel dimers of bis-cysteine peptidesTetrahedron Letters, 1988
- Preparation of Boc‐[S‐(3‐nitro‐2‐pyridinesulfenyl)]‐cysteine and its use for unsymmetrical disulfide bond formationInternational Journal of Peptide and Protein Research, 1986
- The Removal of S‐Cysteine Protection by Means of 2‐Pyridine Sulfenyl Chloride and the Subsequent Formation of Disulfide Bonds. Preliminary communicationHelvetica Chimica Acta, 1979