Synthesis and conformational behavior of pseudopeptides containing δ-azaproline. A cis conformational preference for Xaa1–δ-azaPro bond
Author:
Funder
National Research Agency
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. Stereoselective synthesis of (R)- and (S)-1,2-diazetidine-3-carboxylic acid derivatives for peptidomimetics;Organic & Biomolecular Chemistry;2024
2. δ-Azaproline and Its Oxidized Variants;The Journal of Organic Chemistry;2020-02-26
3. δ-Azaproline: A versatile tool to design pseudopeptides by its incorporation via Nε or Nδ atoms;Tetrahedron Letters;2019-01
4. Conformational studies of new pseudotripeptide with pyrazine amidoxime motif and simplified analogs using IR, NMR spectroscopy, and molecular dynamic simulations;Structural Chemistry;2016-11-29
5. cis–trans-Amide isomerism of the 3,4-dehydroproline residue, the ‘unpuckered’ proline;Beilstein Journal of Organic Chemistry;2016-03-29
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