| Literature DB >> 31984754 |
Jia-Lin Tu1, Jia-Li Liu1, Wan Tang1, Ma Su1, Feng Liu1.
Abstract
Nitrogen-containing heterocycles are prevalent in both naturally and synthetically bioactive molecules. We report herein an unprecedented protocol for radical aza-cyclization of α-imino-oxy acids with pendant alkenes via synergistic photoredox and cobaloxime catalysis. With or without alkenes as the intermolecular cross-coupling partners, the transformation provides a variety of corresponding alkene-containing dihydropyrrole products in satisfactory yields. In the presence of external alkenes, the tandem reaction generates E-selective coupling products with excellent chemo- and stereoselectivity.Entities:
Year: 2020 PMID: 31984754 DOI: 10.1021/acs.orglett.0c00224
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005