The transformation is complete! The total synthesis of theopederin D (see structure), a potent cytotoxin, has been achieved through oxidative cleavage of a carbon–carbon bond. Other key transformations include an acid-mediated functionalization of a tetrahydrofuranol, a syn-selective glycal epoxide ring-opening, and an asymmetric aldehyde/acid chloride condensation.
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Green et al. (2008) studied this question.
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