| Literature DB >> 26212589 |
Michael U Luescher1, Jeffrey W Bode2.
Abstract
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.Entities:
Keywords: SnAP reagents; aldehydes; cross-coupling; homogeneous catalysis; nitrogen heterocycles
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Year: 2015 PMID: 26212589 DOI: 10.1002/anie.201505167
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336