134236-15-0Relevant articles and documents
PREPARATION OF CYCLIC ETHER ACETALS FROM 2-BENZENESULPHONYL DERIVATIVES: A NEW MILD GLYCOSIDATION PROCEDURE
Brown, Dearg S.,Ley, Steven V.,Vile, Sadie
, p. 4873 - 4876 (1988)
Several alcohols ranging from hindered to those containing chemically sensitive groups react with 2-benzenesulphonyl cyclic ethers in the presence of magnesium bromide etherate and sodium bicarbonate to give good yields of the corresponding acetals.
Use of 2-phenylsulphonyl cyclic ethers in the preparation of tetrahydropyran and tetrahydrofuran acetals and in some glycosidation reactions
Brown, Dearg S.,Ley, Steven V.,Vile, Sadie,Thompson, Mervyn
, p. 1329 - 1342 (2007/10/02)
2-Phenylsulphonyl cyclic ethers undergo facile displacement of the sulphonyl group by alcohols, in the presence of magnesium bromide etherate and sodium bicarbonate in tetrahydrofuran, to give goodyields of the corresponding acetals.