Highly Enantioselective Three-Component Direct Mannich Reactions of Unfunctionalized Ketones Catalyzed by Bifunctional Organocatalysts
摘要：
A highly stereoselective three-component direct Mannich reaction between aromatic aldehydes, p-toluenesulfonamide, and unfunctionalized ketones was achieved through an enolate mechanism for the first time with a bifunctional quinidine thiourea catalyst. The corresponding N-tosylated beta-aminoketones were obtained in high yields and excellent diastereo- and enantioselectivities (up to >99:1 dr and >99% ee).
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关键词：
BETA-AMINO KETONES ONE-POT EFFICIENT SYNTHESIS ADDITION-REACTIONS ACID-DERIVATIVES BENZYL CARBAMATE HENRY REACTION ALPHA-AMINO ALDEHYDES THIOUREA
DOI：
10.1021/ol303315c
被引量：
年份：
2013
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