Formula: C7H8O2. Utsumi, T; Noda, K; Kawauchi, D; Ueda, H; Tokuyama, H in [Utsumi, Tatsuki; Noda, Kenta; Kawauchi, Daichi; Ueda, Hirofumi; Tokuyama, Hidetoshi] Tohoku Univ, Grad Sch Pharmaceut Sci, Aoba Ku, Aoba 6-3 Aramaki, Sendai, Miyagi 9808578, Japan published Nitrile Synthesis by Aerobic Oxidation of Primary Amines and in situ Generated Imines from Aldehydes and Ammonium Salt with Grubbs Catalyst in 2020, Cited 64. The Name is m-Methoxyphenol. Through research, I have a further understanding and discovery of 150-19-6.
Herein, a Grubbs-catalyzed route for the synthesis of nitriles via the aerobic oxidation of primary amines is reported. This reaction accommodates a variety of substrates, including simple primary amines, sterically hindered beta,beta-disubstituted amines, allylamine, benzylamines, and alpha-amino esters. Reaction compatibility with various functionalities is also noted, particularly with alkenes, alkynes, halogens, esters, silyl ethers, and free hydroxyl groups. The nitriles were also synthesized via the oxidation of imines generated from aldehydes and NH4OAc in situ.
About m-Methoxyphenol, If you have any questions, you can contact Utsumi, T; Noda, K; Kawauchi, D; Ueda, H; Tokuyama, H or concate me.. Formula: C7H8O2
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