Catalytic Synthesis of N-Unprotected Piperazines, Morpholines, and Thiomorpholines from Aldehydes and SnAP Reagents.

Angew Chem Int Ed Engl

Laboratory of Organic Chemistry, Department of Chemistry and Applied Biosciences, ETH Zurich, Vladimir-Prelog-Weg 3, 8093 Zurich (Switzerland) http://www.bode.ethz.ch.

Published: September 2015

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.201505167DOI Listing

Publication Analysis

Top Keywords

catalytic synthesis
4
synthesis n-unprotected
4
n-unprotected piperazines
4
piperazines morpholines
4
morpholines thiomorpholines
4
thiomorpholines aldehydes
4
aldehydes snap
4
snap reagents
4
reagents commercially
4
commercially snap
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!