1235-22-9Relevant academic research and scientific papers
Boron Trifluoride?Diethyl Ether-Catalyzed Etherification of Alcohols: A Metal-Free Pathway to Diphenylmethyl Ethers
Li, Jiaqiang,Zhang, Xiaohui,Shen, Hang,Liu, Qing,Pan, Jing,Hu, Wen,Xiong, Yan,Chen, Changguo
supporting information, p. 3115 - 3120 (2015/11/03)
A novel boron trifluoride?diethyl ether (BF3?OEt2)-catalyzed etherification procedure has been developed in which primary and secondary alcohols are easily converted into diphenylmethyl ethers with yields of up to 99%.
Enantioselective allyltitanations. Synthesis of optically active 1,2- diol units: Useful intermediates for the preparation of biologically active compounds
Cossy, Janine,Bouzbouz, Samir,Caille, Jean Claude
, p. 3859 - 3862 (2007/10/03)
1,2-Diol units were synthesized with excellent enantiomeric excess by using an enantioselective allyltitanation of α-alkoxy-substituted aldehydes.
Cerium(IV), as a selective and efficient catalyst for alcoholyses of allylic and tertiary benzylic alcohols
Iranpoor, Nasser,Mothaghineghad, Enayatholah
, p. 1859 - 1870 (2007/10/02)
An efficient and selective method is described for the catalytic conversion of allylic, and tertiary benzylic alcohols into their corresponding ethers in the presence of Ce(IV) under solvolytic and non- solvolytic conditions.
Regioselective N- or O-Tritylation of 2(1H)-Pyridone - (Triphenylmethyl)pyridones as Tritylation Agents
Effenberger, Franz,Brodt, Werner,Zinczuk, Juan
, p. 3011 - 3026 (2007/10/02)
Tritylation of 2(1H)-pyridone (1) with triphenylmethyl chloride (4) in acetonitrile leads exclusively to N-trityl-2(1H)-pyridone (3a) via the lithium salt 1', whereas 2-pyridyl trityl ether (3b) is the only product from the reaction with the sodium salt 1
