2,6-Pyridinedicarboxylic acid as organocatalyst for the synthesis of 1,5-benzodiazepines through one-pot reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference38 articles.
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4. Metal-free organocatalysis through explicit hydrogen bonding interactions
5. Asymmetric Catalysis by Chiral Hydrogen-Bond Donors
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1. NiFe2O4@SiO2@PrNH2–DPA–CeCl3: a cerium-based magnetic nano dual-acid catalyst with high efficacy and recyclability for domino sequential synthesis of lactam ring-fused 1,5-benzodiazepines;Catalysis Science & Technology;2023
2. Organocatalysis in Synthetic Heterocyclic Chemistry;Heterocycles;2022-06-17
3. 2,6‐Pyridinedicarboxylic Acid (PDCA) Catalyzed Improved Synthetic Approach for 1‐Amidoalkyl Naphthols, Dihydropyrimidin‐2(1H)‐ones and Bis‐indoles;ChemistrySelect;2021-09-02
4. Crystal structure, Hirshfeld surface analysis and interaction energy calculation of 4-(furan-2-yl)-2-(6-methyl-2,4-dioxopyran-3-ylidene)-2,3,4,5-tetrahydro-1H-1,5-benzodiazepine;Acta Crystallographica Section E Crystallographic Communications;2021-07-27
5. Chalcone derived benzoheterodiazepines for medicinal applications: A Two‐pot and one‐pot synthetic approach;Journal of Heterocyclic Chemistry;2021-07-11
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