A series of highly stereospecific reactions were used in the total synthesis of callipeltoside A (1), thus allowing the assignment of its absolute and relative configuration. a) Schmidt glycosylation, b) Ru Alder–ene coupling, c) Emmons–Wadsworth–Horner olefination, d) chiral auxiliary directed alkylation, e) asymmetric allylic Pd alkylation.
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Trost et al. (2002) studied this question.
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