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01094 am a22002053u 4500 |
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38217 |
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|a dc
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|a Kumar, Raju Suresh
|e author
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|a I. Almansour, Abdulrahman
|e author
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|a Arumugam, Natarajan
|e author
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|a Altaf, Mohammad
|e author
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|a Carlos Menéndez, José
|e author
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|a Kumar, Raju Ranjith
|e author
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|a Osman, Hasnah
|e author
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|a A Sustainable Approach to the Stereoselective Synthesis of Diazaheptacyclic Cage Systems Based on a Multicomponent Strategy in an Ionic Liquid
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260 |
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|b MDPI,
|c 2016.
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|z Get fulltext
|u http://eprints.usm.my/38217/1/A_Sustainable_Approach_to_the_Stereoselective_Synthesis.pdf
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|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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|a en
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|a QD1-999 Chemistry
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