Discovery of a Highly Selective and Efficient Reagent for Formation of Intramolecular Disulfide Bonds in Peptides
- 8 July 2000
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 122 (29), 6809-6815
- https://doi.org/10.1021/ja0008618
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Kinetics and Mechanism for Reduction of the Anticancer Prodrug trans,trans,trans-[PtCl2(OH)2(c-C6H11NH2)(NH3)] (JM335) by ThiolsInorganic Chemistry, 2000
- Kinetics and Equilibria of the Formation and Reduction of the Disulfide Bonds in Arginine-Vasopressin and Oxytocin by Thiol/Disulfide Interchange with Glutathione and CysteineThe Journal of Organic Chemistry, 1994
- Synthesis of .alpha.-conotoxin SI, a bicyclic tridecapeptide amide with two disulfide bridges: illustration of novel protection schemes and oxidation strategiesJournal of the American Chemical Society, 1993
- Dynamics of cis/trans isomerization of the cysteine6-proline peptide bonds of oxytocin and arginine-vasopressin in aqueous and methanol solutionsJournal of the American Chemical Society, 1993
- Cyclization of disulfide‐containing peptides in solid‐phase synthesis†International Journal of Peptide and Protein Research, 1991
- The amino acid sequences of frog heart atrial natriuretic‐like peptide and mammalian ANF are closely relatedFEBS Letters, 1988
- Design of potent antagonists of the vasopressor response to arginine-vasopressinJournal of Medicinal Chemistry, 1978
- Comparative use of benzhydrylamine and chloromethylated resins in solid-phase synthesis of carboxamide terminal peptides. Synthesis of oxytocin derivativesThe Journal of Organic Chemistry, 1977
- Thermochemistry and oxidation potentials of the platinum group metals and their compoundsChemical Reviews, 1968
- Carbon Dichloride as an Intermediate in the Basic Hydrolysis of Chloroform. A Mechanism for Substitution Reactions at a Saturated Carbon Atom1Journal of the American Chemical Society, 1950