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Strategic applications of Baylis-Hillman adducts to general syntheses of 3-nitroazetidines
Authors:Rai Ankita  Yadav Lal Dhar S
Institution:Green Synthesis Lab, Department of Chemistry, University of Allahabad, Allahabad, 211002, India.
Abstract:A novel one-pot highly diastereoselective synthesis of substituted 3-nitroazetidines via an anionic domino process is described. The synthesis involves a high yielding annulation of Baylis-Hillman alcohols and their aldehydes with either N-aryl/tosylphosphoramidates or N-aryl/tosylphosphoramidates in combination with a task-specific ionic liquid bmim]X-Y] to afford the corresponding 1,2,3-tri- and 1,2,3,4-tetrasubstituted azetidines, respectively. Plausible mechanisms for the formation of various 3-nitroazetidines have been suggested.
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