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

ABSTRACT: 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.

SUBMITTER: Suresh Kumar R

PROVIDER: S-EPMC6273701 | biostudies-other | 2016 Jan

REPOSITORIES: biostudies-other

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

Suresh Kumar Raju R Almansour Abdulrahman I AI Arumugam Natarajan N Altaf Mohammad M Menéndez José Carlos JC Kumar Raju Ranjith RR Osman Hasnah H

Molecules (Basel, Switzerland) 20160129 2

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. ...[more]

PMID: 26840282

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