1021906-83-1Relevant academic research and scientific papers
Facile ring-opening of N-acylisatins for the development of novel peptidomimetics
Cheah, Wai Ching,Wood, Kasey,Black, David Stc,Kumar, Naresh
experimental part, p. 7603 - 7610 (2011/10/12)
A range of novel mono- and bis-glyoxylamide peptidomimetics were prepared via the facile ring-opening of N-acylisatins with amino acids and peptide derivatives. The ring-opening of N-acylisatins with dipeptides and tripeptides was discovered to be the mos
Synthesis of anti-bacterial peptidomimetics derived from N-acylisatins
Cheah, Wai Ching,Black, David StC,Goh, Wai Kean,Kumar, Naresh
, p. 2965 - 2968 (2008/09/20)
An efficient synthetic strategy to mono- and bis-glyoxylamide derivatives via the reaction of N-acylisatins with a range of amino acids has been developed. Using this strategy, a series of new peptidomimetics have been synthesized.
