| Literature DB >> 27701812 |
Samuel J Aspin1, Sylvain Taillemaud1, Patrick Cyr1, André B Charette2.
Abstract
A fundamentally simple, mild, and practical procedure for peptide bond formation is reported that employs a stoichiometric amount of easy-to-access 9-silafluorenyl dichlorides as the coupling agent. Without initial preactivation or elaboration of the carboxylic acid or amine termini of the amino acids, the developed reagent is proposed to act through an unprecedented chemical ligation mechanism, bringing the two coupling partners together before being subsequently eliminated. The desired amides or peptide bonds are thus furnished in good yields and with low to no epimerization.Entities:
Keywords: amides; amino acids; peptides; silanes; synthetic methods
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Substances:
Year: 2016 PMID: 27701812 DOI: 10.1002/anie.201606120
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336