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Glucofuranurono-6,3-lactones syntheses with

An improved synthesis based on the same strategy was devised by Driguez and Henrissat [52]. These workers took advantage of the regiospecifically available position C-5 in 1,2-0-iso-propylidene-a-D-glucofuranurono-6,3-lactone (28). This easily accessible starting material was 0-sulfonylated with tosyl chloride followed by reduction of the lactone moiety and... [Pg.2005]

See other pages where Glucofuranurono-6,3-lactones syntheses with is mentioned: [Pg.201]    [Pg.98]    [Pg.231]    [Pg.133]    [Pg.59]    [Pg.163]    [Pg.117]    [Pg.21]   
See also in sourсe #XX -- [ Pg.231 , Pg.232 , Pg.233 ]

See also in sourсe #XX -- [ Pg.33 , Pg.231 , Pg.232 , Pg.233 ]



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