141077-56-7Relevant academic research and scientific papers
Iron-catalyzed asymmetric aerobic oxidative dearomatizing spirocyclization of methylenebis(arenol)s
Kim, Chungsik,Oguma, Takuya,Fujitomo, Chisaki,Uchida, Tatsuya,Katsuki, Tsutomu
, p. 1262 - 1264 (2016)
Iron-catalyzed asymmetric oxidative dearomatization of methylenebis(arenol)s, readily prepared from salicyl alcohol and naphthol derivatives under microwave irradiation, was developed using dioxygen in air as an oxidant. Various enantioenriched spirocyclic compounds were obtained with up to 89% chemical yield and 87% ee.
Oxidation of 1-(2-hydroxybenzyl)-2-naphthols
Kasturi, T R,Charyulu, P V P Pragna,Ganeshprasad, K B
, p. 1108 - 1111 (2007/10/02)
Condensation of salicyl alcohol with 2-naphthols (9a-d) furnishes 1-(2-hydroxybenzyl)-2-naphthols (6a-d).Methylation of 6a gives the dimethyl ester 11, which has also been prepared by Grignard reaction of 2-methoxyphenylmagnesium bromide with 2-methoxy-1-
