The regioselectivity of the reductive ring-cleavage of the acetal ring of 4,6-O-benzylidenehexopyranosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference35 articles.
1. Stereoselective ring-cleavage of 3-O-benzyl- and 2,3-di-O-benzyl-4,6-O-benzylidenehexopyranoside derivatives with the LiAlH4AlCl3, reagent
2. Hydrogenolysis of benzylidene acetals: synthesis of benzyl 2,3,6,2′,3′,4′-hexa-O-benzyl-β-cellobioside, -maltoside, and -lactoside, benzyl 2,3,4,2′,3′,4′-hexa-O-benzyl-β-allolactiside, and benzyl 2,3,6,2′,3′,6′-hexa-O-benzyl-β-lactoside
3. A simple method for the synthesis of benzyl 4-O-benzylhexopyranosides
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