Tetritols anhydro

However, saponification of 2-O-p-tolylsulfonyl-L-erythritol or of 2-O-p-tolylsulfonyl-D-threitol did not furnish any 1,4-anhydro compounds, but only the respective tetritol. 

With the aid of these rules, we have predicted the structures of the acetals which would be expected to result from the benzylidenation, ethylidenation and methylenation of all the tetritols, pentitols and hexi-tols. As will be seen from Table IV, the predicted structures agree very well with the accepted structures of the compounds. The rules explain, too, the syntheses of 3,5-benzylidene- and 3,5-methylene-gluco-[Pg.180]

Anhydro-alditols. - The solvent-free thermal dehydration of tetritols on zeolites has been studied. At temperatures in excess of 250 C a mixture of products is obtained arising predominantly from intramolecular dehydra-... 

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