| Literature DB >> 33492152 |
Spencer P Pitre1, Tyler K Allred2, Larry E Overman2.
Abstract
The addition of tertiary carbon radicals generated from N-(acyloxy)phthalimide esters to cyclic α,β-unsaturated ketones and lactones is markedly enhanced by the addition of substoichiometric amounts of a Ln(OTf)3. The reaction is accomplished by irradiation with visible light in the absence of a photosensitizer and is suggested to proceed by excitation of a ternary electron donor-acceptor complex between the NHPI ester, Hantzsch ester, and a Ln(OTf)3.Entities:
Year: 2021 PMID: 33492152 DOI: 10.1021/acs.orglett.1c00023
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005