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Unfortunately 29, which is formed in roughly similar amount in the acetalization, could not be employed for the purpose. Although methods for the selective cleavage of benzylidene acetals at either the primary or the secondary oxygen are available (see: Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 3rd ed.; Wiley-Interscience: New York, 1999), our efforts failed with the benzyl ether of 29, which consistently gave the undesired bis-primary dibenzyl ether, therefore preventing the use of the whole isomeric mixture of acetals for the convergent synthesis of 32.
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