An article C-Glycosylation enabled by N-(glycosyloxy)acetamides WOS:000531337600010 published article about STEREOSELECTIVE-SYNTHESIS; STEREOCONTROLLED SYNTHESIS; ARYL GLYCOSIDES; O-GLYCOSIDE; DERIVATIVES; REARRANGEMENT; GLYCALS; STRATEGIES; CATALYST; DESIGN in [Liu, Miao; Li, Tian; Wu, Xia; Liu, Meng; Xiong, De-Cai; Ye, Xin-Shan] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100191, Peoples R China; [Li, Bo-Han] Peking Univ, Sch Basic Med Sci, Inst Syst Biomed, Beijing 100191, Peoples R China in 2020.0, Cited 47.0. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6. Safety of m-Methoxyphenol
The C-glycosylation of C-nucleophiles including allyltrimethylsilane, silyl enol ethers and phenols with N-(glycosyloxy)acetamides as glycosyl donors has been realized. This protocol provides a convenient and practical route for the synthesis of alkyl C-glycosides and aryl 2-deoxy-beta-C-glycosides under mild reaction conditions.
About m-Methoxyphenol, If you have any questions, you can contact Liu, M; Li, BH; Li, T; Wu, X; Liu, M; Xiong, DC; Ye, XS or concate me.. Safety of m-Methoxyphenol
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