One-pot catalytic enantioselective synthesis of tetrahydropyridines via a nitro-Mannich/hydroamination cascade.

Org Lett

Department of Chemistry, Chemistry Research Laboratory, University of Oxford, Mansfield Road, Oxford, OX1 3TA, UK.

Published: October 2012

The highly enantioselective preparation of synthetically useful tetrahydropyridine derivatives employing a one-pot nitro-Mannich/hydroamination cascade is reported. This approach utilizes an asymmetric organocatalytic nitro-Mannich reaction followed by a gold-catalyzed alkyne hydroamination/isomerization sequence that yields the desired tetrahydropyridines in good yields and high diastereo- and enantioselectivities.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ol302459cDOI Listing

Publication Analysis

Top Keywords

nitro-mannich/hydroamination cascade
8
one-pot catalytic
4
catalytic enantioselective
4
enantioselective synthesis
4
synthesis tetrahydropyridines
4
tetrahydropyridines nitro-mannich/hydroamination
4
cascade highly
4
highly enantioselective
4
enantioselective preparation
4
preparation synthetically
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!