My watch list  

The chemical ligation of selectively S-acylated cysteine peptides to form native peptides via 5-, 11- and 14-membered cyclic transition states

Alan R. Katritzky, Nader E. Abo-Dya, Srinivasa R. Tala, Zakaria K. Abdel-Samii
(Communication from Org. Biomol. Chem.)
Alan R. Katritzky, Org. Biomol. Chem., 2010, DOI: 10.1039/c003234d
To cite this article before page numbers are assigned, use the DOI form of citation above.
Ontology Terms: carbamate ester; amino acid; hydrochloride; L-cysteine residue; acyl group; L-threonine residue; acyl chloride; peptide; glycine residue; protein; thiol; amino group; carboxy group; dipeptide; hydroxy group; solvent; (fluoren-9-ylmethoxy)carbonyl group; pentapeptide; tetrapeptide; sugar; 13C nuclear magnetic resonance spectroscopy; 1H nuclear magnetic resonance spectroscopy; acylation; amino groups; thioester; high-performance liquid chromatography-mass spectrometry; elemental analysis; S-acylation; aminolysis
Primary Compounds:

The content of this RSS Feed (c) The Royal Society of Chemistry

Authors:   Alan R. Katritzky; Nader E. Abo-Dya; Srinivasa R. Tala; Zakaria K. Abdel-Samii
Journal:   Organic & Biomolecular Chemistry
Volume:   8
edition:   10
Year:   2010
Pages:   2316
DOI:   10.1039/C003234D
Publication date:   07-Apr-2010
Facts, background information, dossiers
More about RSC Publishing
Your browser is not current. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE