Pyrrolidines bearing a quaternary α-stereogenic center. Part 2: Access to proline chimeras, stereoselective approach and mechanistic aspects

D Trancard, JB Tout, T Giard, I Chichaoui, D Cahard…

Index: Trancard, Delphine; Tout, Jean-Baptiste; Giard, Thierry; Chichaoui, Ilhame; Cahard, Dominique; Plaquevent, Jean-Christophe Tetrahedron Letters, 2000 , vol. 41, # 20 p. 3843 - 3847

Full Text: HTML

Citation Number: 20

Abstract

The present work describes the access to various proline chimeras bearing a quaternary α- stereogenic center, via the Duhamel ring contraction of heterocyclic enamines. Attempts to induce diastereoselectivity are reported. The 'chiral enamine'strategy afforded the required aminoaldehydes with diastereomeric ratios as high as 85: 15.