Carb-32. Radicals, Cations, and Anions

Naming procedures described in this section follow the recommendations given in [25], 

Names for radicals are formed in the same way as those for the corresponding substituent groups (see 2-Carb-31.2). 

6-Tetra-0-methyl-D-fructos-4-0-yl Tetra-O-benzyl-D-glucopyranosyl 

Carbenes are named analogously by use of the suffix -yUdene . Example  

Cations produced by formal loss of H from a carbon atom are denoted by replacing terminal e with the suffix -ylium , in conjunction with appropriate locants and a deoxy- prefix if necessary (cf. 2-Carb-31.2). 

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Bivalent and tervalent residues 2-Carb-32. Radicals, cations and anions 2-Carb-33. Glycosides and glycosyl compounds... 

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