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/ol302459c | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!