Use of the benzyl group during purdie methylation: a synthesis of 2-O-methyl-D-mannose
- 30 September 1977
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 58 (1) , 227-229
- https://doi.org/10.1016/s0008-6215(00)83422-9
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Use of the 2,6-dimethoxybenzoyl group to prevent acyl migration during purdie methylation: A synthesis of 2-O-methyl-D-mannoseCarbohydrate Research, 1975
- Synthesis of Methyl 3-O-(3,6-Dideoxy-alpha-D-arabino-hexopyranosyl)-alpha-D-mannopyranoside.Acta Chemica Scandinavica, 1972
- Methylation of carbohydrates bearing base-labile substituents, with diazomethane-boron trifluoride etherate : II. A new synthesis of 2-O-methyl-D-mannoseCarbohydrate Research, 1967
- 933. Methyl 2,3-anhydro-α-D-mannoside and 3,4-anhydro-α-D-altroside and their derivatives. Part IJournal of the Chemical Society, 1962