- Haworth Methylation
-
Haworth Methylation
W. N. Haworth, J. Chem. Soc. 107, 13 (1915).
Formation of methylated methyl glycosides from monosaccharides with dimethyl sulfate and 30% sodium hydroxide. The glycosidic methyl group is hydrolyzed with acid to yield the free methylated sugar:

W. N. Haworth, H. Machemer, J. Chem. Soc. 1932, 2270; C. C. Barker et al., ibid. 1946, 783; E. J. Bourne, S. Peat, Advan. Carbohyd. Chem. 5, 146 (1950); W. Pigman, The Carbohydrates 1957, 369. Cf. Purdie Methylation.
Prev: Haworth Phenanthrene Synthesis
Next: Sommelet-Hauser Rearrangement - 【Back】【Close 】【Print】【Add to favorite 】
- Related information
-
Health and Chemical more >
-
Hot Products
- 527-35-5 2,3,5,6-TETRAMETHYL PHENOL
- 87616-84-0 L-Lysinamide,L-histidyl-D-tryptophyl-L-alanyl-L-tryptophyl-D-phenylalanyl-
- 828-01-3 DL-BETA-PHENYLLACTIC ACID
- 7446-34-6 Selenium sulfide
- 618102-16-2 1-(3-Chloro-4-fluorophenyl)-3-P-tolyl-1H-pyrazole-5-carboxylic acid
- 25487-66-5 3-Carboxyphenylboronic acid
- 596-51-0 Glycopyrrolate
- 363-22-4 13,14-dihydroprostaglandin E2
- 12217-79-7 Disperse Blue 56
- 2511-95-7 1,2-dimethylcyclopropane
- 2825-82-3 Tetrahydrocyclopentadiene
- 628-87-5 Iminodiacetonitrile


