955124-58-0Relevant articles and documents
Model Reactions for the Enantioselective Synthesis of γ-Rubromycin: Stereospecific Intramolecular Photoredox Cyclization of an ortho-Quinone Ether to a Spiroacetal
Wakita, Fumihiro,Ando, Yoshio,Ohmori, Ken,Suzuki, Keisuke
, p. 3928 - 3932 (2018/07/25)
A model study for the enantioselective total synthesis of γ-rubromycin has revealed a promising approach for constructing the chiral, nonracemic bicyclic spiroacetal via the stereospecific photoredox reaction of 1,2-naphthoquinone ether.