| Literature DB >> 30079984 |
Kazuya Honda1, Koichi Mikami1.
Abstract
Highly enantioselective [3+2] cycloaddition of ynones and nitrones has been developed. Very bulky ligand, DTBM-SEGPHOS, was used for an effective asymmetric induction over distal reaction centers on the linear ynone dipolarophile and for prevention of PdII catalyst deactivation by coordination of the nitrones. The reaction has wide scope of substrates in both ynones and nitrones.Entities:
Keywords: alkynes; computational chemistry; cycloaddition; palladium; synthetic methods
Year: 2018 PMID: 30079984 DOI: 10.1002/asia.201801016
Source DB: PubMed Journal: Chem Asian J ISSN: 1861-471X