Use of the benzyl group during purdie methylation: a synthesis of 2-O-methyl-D-mannose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference7 articles.
1. Methylation of carbohydrates bearing base-labile substituents, with diazomethane-boron trifluoride etherate
2. Use of the 2,6-dimethoxybenzoyl group to prevent acyl migration during purdie methylation: A synthesis of 2-O-methyl-D-mannose
3. 933. Methyl 2,3-anhydro-α-D-mannoside and 3,4-anhydro-α-D-altroside and their derivatives. Part I
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1. Relative Reactivity of Hydroxyl Groups in Monosaccharides;Carbohydrates;2009-08-03
2. M;Dictionary of Carbohydrates;1998
3. The Alkylation of Mono- and Disaccharides Via an Initialising Electrochemical Step;Journal of Carbohydrate Chemistry;1993-03
4. Studies of model compounds for the analysis of ester-containing polysaccharides by the reductive-cleavage method;Carbohydrate Research;1992-07
5. The use of aldonolactones for the synthesis of 2-O-methyl-l-rhamnose and 2-O-methyl-d-mannose;Carbohydrate Research;1989-08
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