Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 79, Issue 7, Pages 3094-3102Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo500237j
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Funding
- MIUR (PRIN) [prot. 2010NRREPL]
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A new semirigid dipeptide mimetic was prepared on multigram scale, in good yield, and in a stereocontrolled way, starting from commercially available and unexpensive reagents, i.e., N-benzylpiperidone, tosyl azide, and proline methyl ester. The optimized multicomponent process consisted of a cascade click cycloaddition and a ring rearrangement reaction, followed by a reductive step. Theoretical calculations were performed to elucidate the reaction mechanism and support the stereochemical outcome of the reduction. Finally, the new scaffold was used for the preparation of model peptidomimetics, whose beta turn conformation was confirmed by dynamic NMR experiments.
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