| Literature DB >> 32081000 |
Suva Paria1, Edoardo Carletti1, Michela Marcon1, Alessio Cherubini-Celli1, Andrea Mazzanti2, Marzio Rancan3, Luca Dell'Amico1, Marcella Bonchio1, Xavier Companyó1.
Abstract
Herein is reported the asymmetric allylic benzylation of Morita-Baylis-Hillman (MBH) carbonates with 2-methylbenzophenone (MBP) derivatives as nonstabilized photogenerated C-nucleophiles. The dual activation of both reaction partners, chiral Lewis-base activation of the electrophile and light activation of the nucleophile, enables the stereoselective installation of benzyl groups at the allylic position to forge tertiary and quaternary carbon centers.Entities:
Year: 2020 PMID: 32081000 DOI: 10.1021/acs.joc.0c00175
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354