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A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid MDPI
Journal article   Open access  Peer reviewed

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

Raju Suresh Kumar, Abdulrahman I. Almansour, Natarajan Arumugam, Mohammad Altaf, Jose Carlos Menendez, Raju Ranjith Kumar and Hasnah Osman
Molecules (Basel, Switzerland), Vol.21(2)
01/02/2016
DOI: https://doi.org/10.3390/molecules21020165

Abstract

Biochemistry & Molecular Biology Chemistry Chemistry, Multidisciplinary Life Sciences & Biomedicine Physical Sciences Science & Technology
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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https://doi.org/10.3390/molecules21020165View
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