| Literature DB >> 25065781 |
Iryna O Lebedyeva1, Suvendu Biswas, Kevin Goncalves, Sean M Sileno, Ashton R Jackson, Kunal Patel, Peter J Steel, Alan R Katritzky.
Abstract
Monocarbonyl activation of 2,2-disubstituted malonic acids with benzotriazole leads to decarboxylation of one of the carboxy groups and formation of a CH bond. Intermediate carbonyl benzotriazoles then readily acylate nucleophilic reagents and peptides resulting in libraries of conjugates and peptidomimetics.Entities:
Keywords: acylation; cleavage reactions; conjugates; decarboxylation; peptides
Year: 2014 PMID: 25065781 DOI: 10.1002/chem.201403529
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236