American Chemical Society
ol901480s_si_001.pdf (1.23 MB)

Synthesis of Iriomoteolide-1a C13−C23 Fragment via Asymmetric Conjugate Addition and Julia−Kocienski Coupling Reaction

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journal contribution
posted on 2009-08-20, 00:00 authored by Yen-Jin Chin, Shun-Yi Wang, Teck-Peng Loh
The key C13−C23 fragment toward the total synthesis of iriomoteolide-1a (1) has been constructed from an 1,2-acetonide containing aldehyde 5 via a Julia−Kocienski olefination with the C16−C23 segment 6. The key step involves stereoselective introduction of the C29 methyl group by a highly efficient CuI-Tol-BINAP-catalyzed asymmetric conjugate addition of methylmagnesium bromide to an α,β-unsaturated ester.