Authors Aota, Y; Doko, Y; Kano, T; Maruoka, K in WILEY-V C H VERLAG GMBH published article about TRANSITION-METAL-FREE; ASYMMETRIC-SYNTHESIS; ENANTIOSELECTIVE CONSTRUCTION; FLUORINATED ALCOHOLS; CROSS-COUPLINGS; CYCLOADDITION REACTIONS; PRIVILEGED STRUCTURES; NAZAROV CYCLIZATION; QUATERNARY CENTER; NATURAL-PRODUCTS in [Aota, Yusuke; Doko, Yuki; Kano, Taichi; Maruoka, Keiji] Kyoto Univ, Grad Sch Sci, Dept Chem, Sakyo Ku, Kyoto 6068502, Japan; [Maruoka, Keiji] Kyoto Univ, Grad Sch Pharmaceut Sci, Sakyo Ku, Kyoto 6068501, Japan; [Maruoka, Keiji] Guangdong Univ Technol, Sch Chem Engn & Light Ind, Guangzhou 510006, Peoples R China in 2020, Cited 164. SDS of cas: 150-19-6. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6
Nucleophilic addition to the oxy-allyl cation intermediate has emerged as a promising methodology for functionalization of the alpha-position of carbonyl compounds in an umpolung fashion. However, a structure of available carbon nucleophiles to trap the catalytically generated oxy-allyl cation has been limited to highly nucleophilic ones. Herein, we report the Bronsted acid-catalyzed alpha-arylation of ketones employing less explored phenolic nucleophiles as carbon nucleophiles in the oxy-allyl cation catalysis, affording ketones bearing an all carbon quaternary center at the alpha-position.
SDS of cas: 150-19-6. About m-Methoxyphenol, If you have any questions, you can contact Aota, Y; Doko, Y; Kano, T; Maruoka, K or concate me.
Reference:
Indole alkaloid derivatives as building blocks of natural products from Bacillus thuringiensis and Bacillus velezensis and their antibacterial and antifungal activity study,
,Preparation of Indole Containing Building Blocks for the Regiospecific Construction of Indole Appended Pyrazoles and Pyrroles