A One-Step Conversion of p-Methoxybenzyl Ethers into Methoxymethyl Ethers by the Action of Dimethoxymethane in the Presence of Tin(II) Bromide and Bromomethyl Methyl Ether
- 1 March 1994
- journal article
- Published by Oxford University Press (OUP) in Bulletin of the Chemical Society of Japan
- Vol. 67 (3) , 885-887
- https://doi.org/10.1246/bcsj.67.885
Abstract
No abstract availableThis publication has 6 references indexed in Scilit:
- Chemical-enzymic synthesis of 5'-thio-N-acetyllactosamine: the first disaccharide with sulfur in the ring of the non-reducing sugarJournal of the American Chemical Society, 1992
- Stepwise Reduction of Acetals to the Corresponding Hydrocarbons. A Mild and Effective Transformation via Carbinyl BromidesBulletin of the Chemical Society of Japan, 1991
- Halogenative Allylation and Reduction of Aromatic Acetals by Double Substitution of Alkoxyl Groups in AcetalBulletin of the Chemical Society of Japan, 1991
- The Reaction of Acetals with Silyl Enol Ethers Promoted by the Combination of Tin(II) Chloride and Organic Halide. Novel and Convenient Synthesis of α,β-Unsaturated KetonesBulletin of the Chemical Society of Japan, 1990
- Synthesis of racemic tenellinThe Journal of Organic Chemistry, 1982
- Total syntheses of aflatoxins M1 and G1 and an improved synthesis of aflatoxin B1Journal of the American Chemical Society, 1971