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. 2007 Jan 19;72(2):626-9.
doi: 10.1021/jo0616512.

One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl-protected amines from ketones

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One-pot asymmetric synthesis of either diastereomer of tert-butanesulfinyl-protected amines from ketones

Jessica Tanuwidjaja et al. J Org Chem. .

Abstract

A one-pot method for the asymmetric synthesis of tert-butanesulfinyl-protected amines is described. Condensation of aryl alkyl and dialkyl ketones with tert-butanesulfinamide followed by in situ reduction with the appropriate reagent provides either diastereomer of the sulfinamide products in good yields and with diastereomeric ratios of up to 99:1.

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