An article Reductive Etherification of Aldehydes and Ketones with Alcohols and Triethylsilane Catalysed by Yb(OTf)(3): an Efficient One-Pot Benzylation of Alcohols WOS:000481396200001 published article about CARBONYL-COMPOUNDS; SYMMETRICAL ETHERS; SILANE REDUCTIONS; ACIDIC MEDIA; STEREOSELECTIVE-SYNTHESIS; COUPLING REACTIONS; GENERAL-SYNTHESIS; ESSENTIAL OILS; ARYL; PRODUCTS in [Pelosi, Azzurra; Lanari, Daniela; Temperini, Andrea; Curini, Massimo; Rosati, Ornelio] Univ Perugia, Dipartimento Sci Farmaceut, Via Liceo 1, I-06123 Perugia, Italy in 2019.0, Cited 64.0. Product Details of 100-51-6. The Name is Benzyl Alcohol. Through research, I have a further understanding and discovery of 100-51-6
The one-pot synthesis of symmetrical and unsymmetrical ethers from aldehydes and ketones can be conveniently performed using Yb(OTf)(3) as catalyst and triethylsilane as reducing agent in presence of alcohols. This methodology leads to the synthesis of ether derivatives with good yields. Notably, this process resulted a useful tool to protect alcohols as benzyl ether derivatives using differently substituted benzaldehydes as protecting agents under mild conditions. A plausible mechanism was also proposed.
Product Details of 100-51-6. About Benzyl Alcohol, If you have any questions, you can contact Pelosi, A; Lanari, D; Temperini, A; Curini, M; Rosati, O or concate me.
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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