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A copper-catalyzed sp3–sp3 cross-coupling for fragment coupling in a total synthesis is demonstrated. The diastereo- and enantioselective total synthesis of the 4,6,8,10,16,18-hexamethyldocosanes highlights the synthetic power of deoxypropionate construction based on an ortho-diphenylphosphanylbenzoyl (o-DPPB)-directed and copper-mediated allylic substitution with Grignard reagents (see scheme).
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Herber et al. (2005) studied this question.
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