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00925njm 22002777a 4500 dc Suresh Kumar, Raju author Almansour, Abdulrahman author Arumugam, Natarajan author Altaf, Mohammad author Menéndez Ramos, José Carlos author Kumar, Raju author Osman, Hasnah author 2016 The microwave-assisted three-component reactions of 3,5-bis(E)-arylmethylidene] tetrahydro-4(1H)-pyridinones, acenaphthenequinone and cyclic α-amino acids in an ionic liquid, 1-butyl-3-methylimidazolium bromide, occurred through a domino sequence affording structurally intriguing diazaheptacyclic cage-like compounds in excellent yields. 1420-3049 10.3390/molecules21020165 https://hdl.handle.net/20.500.14352/23900 https://doi.org/10.3390/molecules21020165 https://www.mdpi.com/1420-3049/21/2/165 A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid