124324-94-3Relevant articles and documents
Environmentally friendly tetrahydrofuranylation of alcohols using NaHSO4SiO2 under solvent-free conditions
Kinfe, Henok H.,Terblanche, Sullivan,Tshivhase, Konanani D.,Ravhura, Livhuwani
, p. 272 - 273 (2012)
A simple, environmentally friendly, and efficient tetrahydrofuranylation of alcohols has been developed using NaHSO4SiO2 (0.5 mol%) as a catalyst under solvent-free conditions to yield corresponding THF ethers in good to excellent yi
An efficient and extremely mild method for protecting alcohols as 2-tetrahydrofuranyl ethers
Barks,Gilbert,Parsons,Upeandran
, p. 6249 - 6252 (2007/10/03)
Reaction of primary or secondary alcohols with BrCCl3 and tetrahydrofuran, usually in the presence of 2,4,6-collidine, leads to the formation of 2-tetrahydrofuranyl ethers in good to excellent yield (56-92%). The reaction mechanism is believed to involve a free-radical chain reaction. (C) 2000 Elsevier Science Ltd.
COBALT (II) CHLORIDE CATALYSED ADDITION OF ALCOHOLS ON VINYL ETHERS: A CONVENIENT SYNTHESIS OF MIXED ACETALS
Igbal, Javed,Srivastava, Rajeev Ranjan,Gupta, Kiran Bala,Khan, M. Amin
, p. 901 - 906 (2007/10/02)
Hydroxyl compounds readily add to Vinyl ethers in presence of a catalytic amount of Cobalt (II) Chloride, to give high yields of mixed acetals.