Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5265406 | Tetrahedron Letters | 2013 | 7 Pages |
Abstract
A novel strategy has been developed for the syntheses of (â)-crispine, (â)-benzo[a]quinolizidine, and (â)-salsolidine using (R)-tert-butanesulfinamide as a source of chirality. The approach involves the stereoselective addition of Grignard reagent to chiral N-sulfinyl imine followed by cyclization of the secondary amide with a tethered halide as key steps.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
N. Siva Senkar Reddy, B. Jagan Mohan Reddy, B.V. Subba Reddy,