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Sugars protection

Walsh, A. and Chapman, S.J., Sugars protect desmosome and corneosome glycoproteins from proteolysis, Arch. Dermatol. Res., 283, 174, 1991. [Pg.80]

OPArs, N(R)PAr2, OP(OAr)2, OAsArj, Prj variable configuring the sugar protecting group... [Pg.478]

Nevertheless, even polyalcoholates are obtained following the reaction scheme above, if sugars protected at their anomeric center solved in aprotic media are fed into the decomposer [32]. [Pg.290]

Construction of the oxazine ring of 783 was achieved by cyanation of the 4-amino-4-ethoxycarbonyl-pyrrol-3-yl C-nucleoside 337 with cyanogen bromide, followed by hydrolysis and cyclization of the ester cyanamide 782 with methanolic potassium hydroxide. Removal of the sugar-protective ketal group gave 783, which possessed immunostimulant properties [85TL5785 86JAP(K)86/260094] (Scheme 205). [Pg.293]

See other pages where Sugars protection is mentioned: [Pg.29]    [Pg.56]    [Pg.61]    [Pg.315]    [Pg.222]    [Pg.152]    [Pg.157]    [Pg.127]    [Pg.229]    [Pg.139]    [Pg.140]    [Pg.241]    [Pg.117]    [Pg.15]    [Pg.68]    [Pg.105]    [Pg.703]    [Pg.201]    [Pg.53]    [Pg.91]    [Pg.128]    [Pg.1429]    [Pg.14]    [Pg.2638]    [Pg.35]    [Pg.155]    [Pg.181]    [Pg.209]    [Pg.656]    [Pg.110]    [Pg.342]    [Pg.299]    [Pg.218]    [Pg.220]    [Pg.220]    [Pg.236]    [Pg.253]   
See also in sourсe #XX -- [ Pg.808 ]



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Protecting group for sugars

Sugar derivatives, protected

Sugar protecting groups

Sugars protected

Sugars protection strategies

Wittig reaction with protected sugars

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