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

The microwave-assisted three-component reactions of 3,5-bis(E)-arylmethylidene] tetrahydro-4(1H)-pyridinones, acenaphthenequinone and cyclic �-amino acids in an ionic liquid, 1-butyl-3-methylimidazolium bromide, occurred through a domino sequence affording structurally intriguing diazaheptacyclic ca...

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Bibliographic Details
Main Authors: Kumar, Raju Suresh (Author), I. Almansour, Abdulrahman (Author), Arumugam, Natarajan (Author), Altaf, Mohammad (Author), Carlos Menéndez, José (Author), Kumar, Raju Ranjith (Author), Osman, Hasnah (Author)
Format: Article
Language:English
Published: MDPI, 2016.
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Online Access:Get fulltext
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700 1 0 |a Altaf, Mohammad  |e author 
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520 |a The microwave-assisted three-component reactions of 3,5-bis(E)-arylmethylidene] tetrahydro-4(1H)-pyridinones, acenaphthenequinone and cyclic �-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. 
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