Commercially available SnAP (stannyl amine protocol) reagents allow the transformation of aldehydes and ketones into a variety of N-unprotected heterocycles. By identifying new ligands and reaction conditions, a robust catalytic variant that expands the substrate scope to previously inaccessible heteroaromatic substrates and new substitution patterns was realized. It also establishes the basis for a catalytic enantioselective process through the use of chiral ligands.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/anie.201505167 | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!