Recommanded Product: 105-13-5. Authors Li, HF; Lupp, D; Das, PK; Yang, L; Goncalves, TP; Huang, MH; El Hajoui, M; Liang, LC; Huang, KW in AMER CHEMICAL SOC published article about in [Lupp, Daniel; Das, Pradip K.; Yang, Li; Goncalves, Theo P.; Huang, Mei-Hui; El Hajoui, Marwa; Huang, Kuo-Wei] King Abdullah Univ Sci & Tech, Div Phys Sci & Engn, Thuwal 239556900, Saudi Arabia; [Li, Huaifeng] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, State Key Lab Chem & Mol Engn Med Resources, Guilin 541004, Peoples R China; [Liang, Lan-Chang] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan; [Liang, Lan-Chang] Kaohsiung Med Univ, Dept Med & Appl Chem, Kaohsiung 80708, Taiwan; [Liang, Lan-Chang] Kaohsiung Med Univ, Sch Pharm, Kaohsiung 80708, Taiwan in 2021, Cited 37. The Name is (4-Methoxyphenyl)methanol. Through research, I have a further understanding and discovery of 105-13-5
The traditional Staudinger/aza-Wittig reaction represents one of the most powerful tools for imine formation. However, for this multistep procedure, the sacrificial phosphine has to be used, resulting in difficulties in the purification process and waste disposal at the same time. Here, we report a redox-neutral azide-alcohol imination methodology enabled by a base-metal nickel PN3 pincer catalyst. The one-step, waste-free, and high atom-economical features highlight its advantages further. Moreover, mechanistic insight suggests a non-metal-ligand cooperation pathway based on the observation of an intermediate and density functional theory calculations.
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Reference:
Alcohol – Wikipedia,
,Alcohols – Chemistry LibreTexts