Pivotal intermediates in the total synthesis of brevetoxin A are the BCDE and the GHIJ ring systems. Several of the previously developed methodologies such as hydroxy epoxide cyclizations, hydroxy dithioketal cyclizations, and Pd-catalyzed coupling with bis(cyclic ketene acetal phosphates) were employed to achieve these synthetic goals.
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Nicolaou et al. (1999) studied this question.
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