Stereoselective Lewis Acid Mediated (3+2) Cycloadditions of N‐H‐ and N‐Sulfonylaziridines with Heterocumulenes |
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Authors: | Robert A Craig II Nicholas R O'Connor Dr Alexander F G Goldberg Prof Brian M Stoltz |
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Institution: | Warren and Katharine Schlinger Laboratory for Chemistry and Chemical Engineering, Division of Chemistry and Chemical Engineering, California Institute of Technology, 1200 E California Blvd, MC 101‐20, Pasadena, CA 91125 (USA) |
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Abstract: | Alkyl and aryl isothiocyanates and carbodiimides are effective substrates in (3+2) cycloadditions with N‐sulfonyl‐2‐substituted aziridines and 2‐phenylaziridine for the synthesis of iminothiazolidines and iminoimidazolidines. Additionally, the stereoselective (3+2) cycloaddition of N‐H‐ and N‐sulfonylaziridines with isothiocyanates can be accomplished, allowing for the synthesis of highly enantioenriched iminothiazolidines. Evidence for an intimate ion‐pair mechanism is presented herein in the context of these chemo‐, regio‐, and diastereoselective transformations. The demonstrated ability to remove the sulfonyl group from the heterocyclic products displays the utility of these compounds for further derivatization and application. |
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Keywords: | cycloadditions heterocumulenes heterocycles Lewis acids stereoselectivity |
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