anti-Selective, Catallytic Asymmetric Vinylogous Mukaiyama Mannich Reactions of Pyrrole-Based Sillyl Dienolates with N-Aryl Aldimines

作者:Curti Claudio*; Battistini Lucia; Ranieri Beatrice; Pelosi Giorgio; Rassu Gloria; Casiraghi Giovanni; Zanardi Franca
来源:Journal of Organic Chemistry, 2011, 76(7): 2248-2252.
DOI:10.1021/jo1021234

摘要

Pyrrole-based silyl dienolates undergo asymmetric vinylogous Mukaiyama Mannich reactions with a series of N-aryl aldimines in the presence of the Hoveyda-Snapper amino acid-derived silver(I) catalysts. The Manrdch products alpha,beta-unsaturated delta-ammo-gamma-butyrolactams-are typically obtained in high yields, excellent gamma-site selectivities and anti-diastereoselectivities, and up to 80% enantioselectivity.

  • 出版日期2011-4-1