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Chloroacetate protecting groups

This ester was designed as a protective group for the 2-position in glycosyl donors. It has the stability of the benzoate during glycosylation, but has the ease of removal of the chloroacetate. It is readily introduced through the acid chloride... [Pg.191]

There is a very large number of different ester protecting groups available and only the more common representatives in carbohydrate chemistry will be treated here. This includes acetate and substituted acetates such as chloroacetate, pivaloate, and levulinate groups. Aroyl groups are frequently used, such as benzoyl and substituted benzoyl e. g. p-phenylbenzoyl and 2,4,6-trimethylbenzoyl groups. [Pg.130]

See other pages where Chloroacetate protecting groups is mentioned: [Pg.130]    [Pg.433]    [Pg.63]    [Pg.12]    [Pg.113]    [Pg.130]    [Pg.433]    [Pg.63]    [Pg.12]    [Pg.113]    [Pg.100]    [Pg.5]    [Pg.367]    [Pg.118]    [Pg.1149]    [Pg.5]    [Pg.367]    [Pg.214]    [Pg.42]    [Pg.10]    [Pg.10]    [Pg.437]    [Pg.177]    [Pg.222]    [Pg.325]    [Pg.77]    [Pg.88]    [Pg.137]    [Pg.608]    [Pg.84]    [Pg.269]    [Pg.325]    [Pg.57]    [Pg.68]    [Pg.24]    [Pg.3]    [Pg.475]    [Pg.118]    [Pg.239]    [Pg.346]    [Pg.198]    [Pg.907]    [Pg.243]    [Pg.89]    [Pg.198]    [Pg.356]    [Pg.357]    [Pg.198]    [Pg.224]    [Pg.263]    [Pg.15]    [Pg.65]    [Pg.207]   
See also in sourсe #XX -- [ Pg.11 ]



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Chloroacetate

Chloroacetate group

Chloroacetates

Chloroacetic

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