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Stereo-, Regio-, and Chemoselective [3 + 2]-Cycloaddition of (2E,4E)-Ethyl 5-(Phenylsulfonyl)penta-2,4-dienoate with Various Azomethine Ylides, Nitrones, and Nitrile Oxides: Synthesis of Pyrrolidine, Isoxazolidine, and Isoxazoline Derivatives and a Computational Study
Kalapattukuppuswamy Kuppuswamy B. Balasubramanian
Published in American Chemical Society
2016
Volume: 81
   
Issue: 6
Pages: 2340 - 2354
Abstract
One-pot chemo-, regio-, and stereoselective synthesis of series of heterocyclic and spiroheterocyclic compounds was accomplished through mono- and bis[3 + 2]-cycloaddition reactions of (2E,4E)-ethyl 5-(phenylsulfonyl)penta-2,4-dienoate as a dipolarophile with azomethine ylides, nitrones, and nitrile oxides in good yields. The structures of the products were established by spectroscopic techniques as well as by single-crystal XRD study, and DFT calculations were performed to further understand the mechanism of this [3 + 2]-cycloaddition reaction. © 2016 American Chemical Society.
About the journal
JournalData powered by TypesetJournal of Organic Chemistry
PublisherData powered by TypesetAmerican Chemical Society
ISSN00223263
Open AccessNo
Concepts (31)
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    Cyanides
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    Cycloaddition
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    Ketones
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    Nitrogen oxides
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    Single crystals
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    Stereochemistry
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    Stereoselectivity
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    AZOMETHINE YLIDES
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    Chemoselective
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    Computational studies
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    Cycloaddition reaction
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    Dft calculation
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    Single crystal xrd
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    Spectroscopic technique
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    Stereoselective synthesis
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    Synthesis (chemical)
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    AZOMETHINE YLIDE
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    ISOXAZOLIDINE DERIVATIVE
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    ISOXAZOLINE DERIVATIVE
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    Nitrile oxide
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    Nitrone
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    Pyrrolidine derivative
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    Article
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    Carbon nuclear magnetic resonance
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    Chemical structure
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    Density functional theory
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    Geometry
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    Molecular mechanics
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    ONE-POT
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    Proton nuclear magnetic resonance
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    X ray diffraction