Use of the 2,6-dimethoxybenzoyl group to prevent acyl migration during purdie methylation: A synthesis of 2-O-methyl-D-mannose
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference26 articles.
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1. Protecting Groups at the Secondary Positions of Carbohydrates;Protecting Groups;2018-11-19
2. The Alkylation of Mono- and Disaccharides Via an Initialising Electrochemical Step;Journal of Carbohydrate Chemistry;1993-03
3. The use of aldonolactones for the synthesis of 2-O-methyl-l-rhamnose and 2-O-methyl-d-mannose;Carbohydrate Research;1989-08
4. An improved method for selective substitution on O-3 of D-mannose. Application to the synthesis of methyl 3-O-methyl-and 2-O-α-Dmannopyranosides;Carbohydrate Research;1978-01
5. Use of the benzyl group during purdie methylation: a synthesis of 2-O-methyl-D-mannose;Carbohydrate Research;1977-09
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