One-pot synthesis of vinylisoxazolidines from simple hydroxylamines and conjugated carbonyls |
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Authors: | Dylan J Quinn Lauren N Tumbelty Erica M Moscarello Alyson N Paneque Amy H Zinsky Maxim P Russ Graham J Haun Nicholas A Cinti Ross M Dare Gustavo Moura-Letts |
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Institution: | Department of Chemistry and Biochemistry, Rowan University, 201 Mullica Hill Rd., Glassboro, NJ 08028, USA |
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Abstract: | Herein is reported the highly chemo- and regioselective synthesis of 3-vinyl-4-formyl and 3-vinyl-5-formylisoxazolidines from enals, hydroxylamines and dipolarophiles under thermal conditions. The reaction works in high yields for a large array of substituted enals and a variety of dipolarophiles. The reaction provides the respective isoxazolidines with high chemoselectivity, stereospecificity and diastereoselectivity without significant purification. The substitution pattern on the dipolarophile directs the regioselectivity of the reaction to provide either 3,4- or 3,5-substituted isoxazolidine isomers. This method provides access to a wide variety of highly substituted, stereochemically dense isoxazolidine scaffolds from the selective reaction of the three proposed components. |
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Keywords: | Isoxazolidines Vinylnitrones Dipolar cycloaddition Dipolarophiles |
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