Synthesis of Spiropyrrolidines and Spiropyrrolizidines by Azomethine Ylide Cycloaddition of Baylis-Hillman Adducts Derived from N-Methyl Maleimide
Author:
Publisher
Georg Thieme Verlag KG
Subject
Organic Chemistry
Link
http://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-0030-1258810.pdf
Cited by 14 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Enantioselective MW-US-assisted Synthesis, DFT Simulation and Molecular Docking of Spiro Pyrrolidine-2,3'-Thieno [2,3-d]Pyridazin-Hydrazide as Green Agricultural Product;Polycyclic Aromatic Compounds;2023-07-04
2. Synthesis, biological evaluation, density functional calculation and molecular docking analysis of novel spiropyrrolizidines derivatives as potential anti-microbial and anti-coagulant agents;Journal of Molecular Structure;2022-02
3. Diastereoselective synthesis of dispiro[indoline-3,3′-furan-2′,3′′-pyrrolidine] via [3 + 2]cycloaddition reaction of MBH maleimides of isatins and 1,3-dicarbonyl compounds;Organic Chemistry Frontiers;2020
4. Solvent-free implementation of two dissimilar reactions using recyclable CuO nanoparticles under ball-milling conditions: synthesis of new oxindole-triazole pharmacophores;Green Chemistry;2017
5. Synthesis of Spirooxindoles Bearing Iminothiolactone Moiety from Morita-Baylis-Hillman Carbonates of Isatins and Phenyl Isothiocyanate;Bulletin of the Korean Chemical Society;2016-12-28
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