Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Reduction, of glycosyl azides

Fig. 11. Synthesis of glycosyl amine by reduction of glycosyl azide (88,95). Fig. 11. Synthesis of glycosyl amine by reduction of glycosyl azide (88,95).
The use of Pd/C (87,89), neutral Raney Ni (W-2) (91,95), and Lyndlar s catalyst (90) have been reported in literature. Conditions used for the reduction of glycosyl azide have to be carefully optimized in order to suppress anomerization and the formation of undesired a-glycosides. Use of basic conditions and procedures that avoid noble metals leads to decreased a-glycosides formation (94). [Pg.202]

Scheme 1 (a) Synthesis of glycosyl azide, (b) Reduction of glycosyl azide to the corresponding glycosylamine followed... [Pg.59]

Thiem et al. have described [75,76] the synthesis of hexopyranosyl imides of gluco and manno configuration starting from 0-protected glycosylamines available by reduction of glycosyl azides. Reaction of 52, 53 with succinic anhydride followed by a cycHzation reaction of the corresponding... [Pg.42]

Figure 2. /V-linked glycopeptides can be obtained by acylation of glycosyl amines, prepared either by reduction of glycosyl azides or directly from reducing sugars. Figure 2. /V-linked glycopeptides can be obtained by acylation of glycosyl amines, prepared either by reduction of glycosyl azides or directly from reducing sugars.
Glycosyl azides are an important family of carbohydrate derivatives. They have been used as precursors of glycopeptides and heterocyclic M-glycosides. The corresponding glycosylamines, which can be obtained by reduction of the azide group, can be used as precursors to glycopolymers or hyper-branched dendrimers, after A-acryloylation. Furthermore, azide functionalities can be easily converted into... [Pg.257]

Warren and associates (18) have prepared a glycosyl azide derivative (15) of a heptasaccharide. This glycosyl azide was obtained from O-a-D-manno-pyranosyl-( 1 — 6)-0-[a-D-mannopyranosyl-( 1 — 3)-(9-a-D-mannopyrano syl-(l— 6)-0-a-D - mannopyranosyl - (1 — 3)] - O-fi- d - mannopyranosyl -(1 — 4) - O - (2 - acetamido - 2 - deoxy-/ -d-glucopyranosyl) - (1 — 4) - 2 -acetamido-2-deoxy-D-glucopyranose (12) by treatment of its peracetylated derivative 13 with trimethylsilyl trifuoromethanesulfonate, followed by reaction of the intermediary oxazoline 14 with trimethylsilyl azide. Reduction of the glycosyl azide 15 in the presence of Lindlar catalyst gave the glycosyla-mine derivative 16. The condensation of 16 with 1-tert-butyl N-(9-fluoren-... [Pg.279]


See other pages where Reduction, of glycosyl azides is mentioned: [Pg.285]    [Pg.199]    [Pg.792]    [Pg.493]    [Pg.782]    [Pg.103]    [Pg.134]    [Pg.141]    [Pg.198]    [Pg.476]    [Pg.285]    [Pg.199]    [Pg.792]    [Pg.493]    [Pg.782]    [Pg.103]    [Pg.134]    [Pg.141]    [Pg.198]    [Pg.476]    [Pg.84]    [Pg.232]    [Pg.301]    [Pg.87]    [Pg.164]    [Pg.273]    [Pg.300]    [Pg.122]    [Pg.793]    [Pg.1638]    [Pg.1643]    [Pg.179]    [Pg.445]    [Pg.783]    [Pg.304]    [Pg.58]    [Pg.466]    [Pg.250]    [Pg.41]    [Pg.201]    [Pg.321]    [Pg.57]    [Pg.131]    [Pg.248]    [Pg.83]    [Pg.77]    [Pg.318]    [Pg.278]    [Pg.166]    [Pg.261]    [Pg.268]    [Pg.286]    [Pg.293]   
See also in sourсe #XX -- [ Pg.134 , Pg.135 , Pg.136 , Pg.137 , Pg.138 , Pg.139 , Pg.140 , Pg.141 ]




SEARCH



Azides, reduction

Glycosyl azides

Reduction of azides

© 2024 chempedia.info