4.8 Article

Stereoselective Organocatalytic One-Pot α,α-Bifunctionalization of Acetaldehyde by a Tandem Mannich Reaction/Electrophilic Amination

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ORGANIC LETTERS
卷 13, 期 21, 页码 5778-5781

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AMER CHEMICAL SOC
DOI: 10.1021/ol202340p

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  1. CNRS
  2. University of Versailles-St-Quentin-en-Yvelines
  3. MENRT

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The first asymmetric organocatalyzed one-pot alpha,alpha-bifunctionalization of acetaldehyde with two different electrophiles is described. A diarylprolinol silyl ether-catalyzed reaction of acetaldehyde with an imine and di-tert-butyl azodicarboxylate affords syn-2,3-diaminoalcohols with excellent ee values of up to 98%. This methodology was successfully applied to the synthesis of a chiral alpha,beta-diaminocarboxylic acid.

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