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It is worth pointing out that the presence of a stoichiometric amount of water was necessary for successful cross-coupling reactions. This observation is consistent with studies previously reported by Johnson and Braun; see ref 45c.
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Although triol acid 42 was isolated as a side product during the deprotection of the benzylidene, the amount obtained was sufficient to attempt macrocyclization. When this material was subjected to the identical macrocyclization conditions used before, a complicated mixture of monolides and diolides was obtained.
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2O) proved unsuccessful as the C8 epoxide opening and/or decomposed products were obtained.
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