1,3,5,8-Tetrasubstituted 1,3,4-Benzotriazepin-2-one Scaffolds for β-Turn Mimicry without Stereogenic Carbon Centers: Synthesis and Conformational Analysis
Author:
Affiliation:
1. Département de Chimie, Université de Montréal, 1375 Ave. Thérèse-Lavoie-Roux, Montréal, Québec H2V 0B3, Canada
Funder
Canadian Institutes of Health Research
Fonds de Recherche du Qu?bec - Nature et Technologies
Natural Sciences and Engineering Research Council of Canada
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.3c00113
Reference33 articles.
1. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists
2. 1,3‐Diazepine: A privileged scaffold in medicinal chemistry
3. Do benzodiazepines mimic reverse-turn structures?
4. Protein β-turn mimetics I. Design, synthesis, and evaluation in model cyclic peptides.
5. γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate
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1. Urotensin II Receptor Modulation with 1,3,4-Benzotriazepin-2-one Tetrapeptide Mimics;Journal of Medicinal Chemistry;2023-10-06
2. Synthesis of 4-Aryl-1,3,4-benzotriazepinones from Isatoic Anhydrides and Hydrazonyl Chlorides;The Journal of Organic Chemistry;2023-05-11
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