𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of the methyl thioglycosides of four stereoisomers and the 2-methoxy derivative of l-fucose

✍ Scribed by Akira Hasegawa; Mitsutoshi Kato; Takashi Ando; Hideharu Ishida; Makoto Kiso


Publisher
Elsevier Science
Year
1995
Tongue
English
Weight
519 KB
Volume
274
Category
Article
ISSN
0008-6215

No coin nor oath required. For personal study only.

✦ Synopsis


The methyl 1-thioglycoside derivative of 2-epi-, 2,4-di-epi-, 3-epi-, 4-epi, and 2-O-methyl-Lfucopyranose have been prepared as glycosyl donors for the synthesis of sialyl Le x ganglioside analogues containing modified Ot-L-fucopyranose residues.


πŸ“œ SIMILAR VOLUMES


Synthesis of the methyl thioglycosides o
✍ Akira Hasegawa; Takashio Ando; Mitsutoshi Kato; Hideharu Ishida; Makoto Kiso πŸ“‚ Article πŸ“… 1994 πŸ› Elsevier Science 🌐 English βš– 883 KB

Methyl thioglycoside derivatives of 2-, 3-, and 4-deoxy-L-fucopyranose have been prepared as glycosyl donors for the synthesis of sialyl IA? ganglioside analogues containing modified a-L-fucopyranose residues. Reductive dethioacylation of 2-(trimethylsilyl)ethyl 3,4-di-O-benzoyl-2-O-(phenoxy)thiocar

The stereospecific synthesis of all four
✍ Edouard Lier; Richard Berthold; Franz Troxler πŸ“‚ Article πŸ“… 1979 πŸ› John Wiley and Sons 🌐 German βš– 534 KB

## Abstract Epoxidation of 3‐phenoxycyclohexene **5** with __m__‐chloro‐perbenzoic acid gave **6** and **7** in a ratio of 9:1. These two epoxides were heated with a series of amines to give the aminophenoxycyclohexanol derivatives **1** and **2** respectively; in all cases the reaction was regio‐

Asymmetric Synthesis and Structure-Activ
✍ Sun-Young Sung; Manfred Kist; August W. Frahm πŸ“‚ Article πŸ“… 1997 πŸ› John Wiley and Sons 🌐 English βš– 291 KB

The stereoisomers of amidinomycin 7 and their intermediates 1-6, which are produced from homochiral 3-oxocyclopentanecarboxylic acids by asymmetric synthesis, are tested for their antimicrobial effects by agar diffusion test and by Bouillon serial dilution assay. Their antibiotic activities against

Pheromone synthesis, CIX. Synthesis of t
✍ Mori, Kenji ;Igarashi, Yasuhiro πŸ“‚ Article πŸ“… 1988 πŸ› John Wiley and Sons 🌐 English βš– 406 KB

The synthesis or thc Tour stereoisomers or 6,12-dimethyl-2-penladecanone (I), the sex pheromone of the banded cucumber beetle IDicihrorico hulfaato LeConte), was achieved employing the rnaniiomcrs aT citroncllol (2) as the starting materials.