Partiell benzylierte Kohlenhydrate, 3: Gezielte Regioselektivität bei der Benzylierung eines Lactosids
Author:
Affiliation:
1. Organisch‐Chemisches Institut der Universität Münster, D‐4400 Münster, Orléans‐Ring 23
Publisher
Wiley
Subject
Inorganic Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/cber.19761090406
Reference15 articles.
1. Partiell benzylierte Kohlenhydrate, 2. Synthese aller Methyl-mono-, Methyl-di- und Methyl-tri-O-benzyl-α-D-glucopyranoside.
2. J. M.Küster I.DyongundG.Huhn unveröffentl.
3. Selective benzylation of some D-galactopyranosides. Unusual relative reactivity of the hydroxyl group at C-4
4. Über synthesen von sphingolipiden. I. einfache synthese des phenyl-2,3,6-tri-O-benzyl-β-D-galaktopyranosids
5. 3,6-Di-O-methyl-D-galactosamine Hydrochloride (2-Amino-2-deoxy-3,6-di-O-methyl-D-galactose Hydrochloride)1
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1. SYNTHESIS OF 2,3-DIDEOXY-d-arabino-HEPTONO-1,4-LACTONEviaA WITTIG REACTION ON UNPROTECTED d-ARABINOSE;Organic Preparations and Procedures International;1992-02
2. Glycosyl imidates. 49. Synthesis of the octasaccharide moiety of the dimeric Lex antigen;Liebigs Annalen der Chemie;1991-05-16
3. Glycosyl Imidates, 42 Selectively Protected Lactose and 2-Azido Lactose, Building Blocks for Glycolipid Synthesis;Liebigs Annalen der Chemie;1989-11-13
4. Synthesis of 3- and 2′-fucosyl-lactose and 3,2′-difucosyl-lactose from partially benzylated lactose derivatives;Carbohydrate Research;1986-10
5. Synthesis of O-(β-d-glucopyranosyluronic acid)-(1→3)-O-β-d-galactopyranosyl-(1→4)-d-glucopyranose;Carbohydrate Research;1986-01
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