A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid

Suresh Kumar, RajuAlmansour, AbdulrahmanArumugam, NatarajanAltaf, MohammadMenéndez Ramos, José CarlosKumar, RajuOsman, Hasnah2023-06-182023-06-1820161420-304910.3390/molecules21020165https://hdl.handle.net/20.500.14352/23900The 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.engAtribución 3.0 Españahttps://creativecommons.org/licenses/by/3.0/es/A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquidjournal articlehttps://doi.org/10.3390/molecules21020165https://www.mdpi.com/1420-3049/21/2/165open access547diazaheptacyclic cage compoundsmulticomponent reactionsionic liquidmicrowaveassisted synthesisQuímica farmaceútica2390 Química Farmacéutica