1,3,5-Tri- and 1,3,4,5-Tetra-Substituted 1,4-Diazepin-2-one Solid-Phase Synthesis
Author:
Affiliation:
1. Département de Chimie, Université de Montréal, C.P. 6128, Succursale Centre Ville, Montréal, Québec, Canada H3C 3J7
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/cc8001052
Reference25 articles.
1. Methods for drug discovery: development of potent, selective, orally effective cholecystokinin antagonists
2. Synthesis of a Trisubstituted 1,4-Diazepin-3-one-Based Dipeptidomimetic as a Novel Molecular Scaffold
3. Modular Synthesis of Cyclic Peptidomimetics Inspired by γ-Turns
4. 1,4-Diazepinone and Pyrrolodiazepinone Syntheses via Homoallylic Ketones from Cascade Addition of Vinyl Grignard Reagent to α-Aminoacyl-β-amino Esters
5. Synthesis of pyrimido[1,4]diazepin-2-one analogs and their evaluation as anticonvulsant agents
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5. γ-Turn Mimicry with Benzodiazepinones and Pyrrolobenzodiazepinones Synthesized from a Common Amino Ketone Intermediate;Organic Letters;2015-06-30
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