Total Synthesis of the Potent HIF-1 Inhibitory Antitumor Natural Product, (8R)-Mycothiazole, via Baldwin–Lee CsF/CuI sp³–sp²-Stille Cross-Coupling. Confirmation of the Crews Reassignment

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A convenient asymmetric total synthesis of the potent HIF-1 inhibitory antitumor natural product, (-)- or (+)-(8R)-mycothiazole (1), is described. Not only does our synthesis confirm the 2006 structural reassignment made by Crews ( Crews , P. , et al. J. Nat. Prod. 2006 , 69 , 145 ), it revises the [α]D data previously reported for this molecule in MeOH from -13.7° to +42.3°. The newly developed route to (8R)-1 sets the C(8)-OH stereocenter via Sharpless AE/2,3-epoxy alcohol reductive ring opening and utilizes two Baldwin-Lee CsF/cat. CuI Stille cross-coupling reactions with vinylstannanes 8 and 3 to efficiently elaborate the C(1)-C(4) and C(14)-C(18) sectors.