| Literature DB >> 28813158 |
Moritz K Jackl1, Luca Legnani2, Bill Morandi2, Jeffrey W Bode1.
Abstract
Photocatalytic coupling of aldehydes and silicon amine protocol (SLAP) reagents enables the simple, scalable synthesis of substituted morpholines, oxazepanes, thiomorpholines, and thiazepanes under continuous flow conditions. Key to the success of this process is the combination of an inexpensive organic photocatalyst (TPP) and a Lewis acid additive, which form an amine radical cation that is easily reduced to complete the catalytic cycle. Di- and trisubstituted SLAP reagents are formed in one step by an iron-catalyzed aminoetherification of olefins.Entities:
Year: 2017 PMID: 28813158 DOI: 10.1021/acs.orglett.7b02395
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005