Studies of Tritylated Pentoses and 6-Deoxyhexoses. II. Trityl Ethers of Methyla- and β-L-Rhamnopyranoside and Their Derivatives
Author:
Publisher
The Chemical Society of Japan
Subject
General Chemistry
Link
https://www.jstage.jst.go.jp/article/bcsj1926/52/10/52_10_3109/_pdf
Reference8 articles.
1. Studies of Tritylated Pentoses and Methyl Pentoses. I. TheO-Tritylation of Methyl α-D-Fucopyranoside
2. Relative Reactivities of Hydroxyl Groups in Carbohydrates
3. Spectroscopic Properties of Methyl Triacetyl-alpha- and beta-L-Rhamnosides.
4. Studies of Tritylated Sucrose. I. Mono-O-tritylsucroses
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1. Synthesis ofβ-D-Ribofuranosyl-(1→3)-α-L-rhamnopyranosyl-(1→3)-L-rhamnopyranose by in situ Activating Glycosylation Using 1-OH Sugar Derivative and Me3SiBr–CoBr2–Bu4NBr–Molecular Sieves 4A System;Bulletin of the Chemical Society of Japan;2001-09
2. Tris(4-bromophenyl)aminium hexachloroantimonate-mediated glycosylations of selenoglycosides and thioglycosides. Evidence for single electron transfer?11This paper is dedicated, with respect and gratitude, to the memory of Margaret A. Clark.;Carbohydrate Research;1998-08
3. Linear dependence of the glycosylation stereoselectivity ofO-trityl ethers by carbohydrate 1,2-O-cyanoalkylidene derivatives on anion concentrations. Effect of substituents in the glycosyl acceptor and a new mechanism of 1,2-cis-glycosides formation;Russian Chemical Bulletin;1995-06
4. Reactivity of sugar trityl ethers in trityl?cyanoalkylidene condensation;Russian Chemical Bulletin;1993-11
5. Studies of Tritylated Pentoses and 6-Deoxyhexoses. III. TheO-Tritylation of Methyl α- and β-D-Xylopyranoside;Bulletin of the Chemical Society of Japan;1983-10
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