Article ID Journal Published Year Pages File Type
5279130 Tetrahedron Letters 2011 4 Pages PDF
Abstract

A chiral acid-base organocatalyst was found to promote an aza-MBH domino process between α,β-unsaturated carbonyl compounds and N-tosylimines to afford tetrahydropyridine derivatives with high enantioselectivity.

Graphical abstractDownload full-size image

Keywords
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
An enantioselective organocatalyzed aza-MBH domino process: application to the facile synthesis of tetrahydropyridines
Authors
, , ,