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Constructing Cyclic Peptides Using an On-Tether Sulfonium Center
Published on: September 28, 2022
Total synthesis of cyclocitropside A and its conversion to cyclocitropsides B and C via asparagine deamidation
Robert E Thompson1, Richard J Payne, Katrina A Jolliffe
1School of Chemistry, The University of Sydney, NSW 2006, Australia.
Organic Letters
|September 21, 2012
Abstract:
The total syntheses of three closely related cyclic peptide natural products, cyclocitropsides A-C, are described. Cyclocitropside A could be readily converted into cyclocitropsides B and C through an asparagine deamidation pathway, indicating that this is a plausible biosynthetic route to these compounds.
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