The isopropylsulfinyl group: A useful chiral controller for the asymmetric aziridination of sulfinylimines and the organocatalytic allylation of hydrazones

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Abstract

(Chemical Equation Presented) A comparative study shows that the isopropylsulfinyl group for which an enantiodivergent and highly diastereoselective approach is reported behaves better than the tert-butylsulfinyl and p-tolylsulfinyl groups, both in terms of reactivity and stereoselectivity in the Corey-Chaykovsky reaction of chiral sulfinylimines and the organocatalytic allylation of acyl hydrazones. © 2005 American Chemical Society.

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Fernández, I., Valdivia, V., Gori, B., Alcudia, F., Álvarez, E., & Khiar, N. (2005). The isopropylsulfinyl group: A useful chiral controller for the asymmetric aziridination of sulfinylimines and the organocatalytic allylation of hydrazones. Organic Letters, 7(7), 1307–1310. https://doi.org/10.1021/ol050080h

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