Regio- and stereoselectivity of the 1,3-dipolar cycloaddition of azomethine ylides to 3-nitro-2(1H)-quinolinone derivatives: A new synthesis of Pyrrolo[3,4-c] quinolines
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference37 articles.
1. Rovati, L.C.; Macovec, F.; Cappelli, A.; Vomero, S.; Anzini, M.; EP1018512.
2. Design, Synthesis, and Preliminary Biological Evaluation of Pyrrolo[3,4-c]quinolin-1-one and Oxoisoindoline Derivatives as Aggrecanase Inhibitors
3. 1,3-Dioxo-4-methyl-2,3-dihydro-1H-pyrrolo[3,4-c]quinolines as potent caspase-3 inhibitors
4. Synthesis and Structure−Activity Relationship of 4-Substituted 2-(2-Acetyloxyethyl)-8-(morpholine- 4-sulfonyl)pyrrolo[3,4-c]quinoline- 1,3-diones as Potent Caspase-3 Inhibitors
5. Microwave-Assisted Synthesis of Diverse Pyrrolo[3,4-c]quinoline-1,3-diones and Their Antibacterial Activities
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1. Synthesis of spiro[piperidine-4,3′-pyrrolo[3,4-c]quinolines via 1,3-dipolar cycloaddition of azomethine ylides and 3-Nitro-2(1H)-quinolones;Tetrahedron Letters;2024-04
2. Diastereoselective cycloaddition of isatin derived azomethine ylides to 3-nitro-2(1H)-quinolones;Tetrahedron;2024-03
3. Decarboxylative 1,3-dipolar cycloadditions of l-proline;RSC Advances;2024
4. Diastereoselective construction of carbazole‐based spiropyrrolidines and spiropyrrolizidines via cycloaddition reaction;Journal of Heterocyclic Chemistry;2023-10-11
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