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- W2986435102 abstract "The total synthesis of endolides A and B has been achieved in a concise and highly stereoselective fashion (12 steps; 16.2 and 16.0% overall yield, respectively). Key features of the route include a modified Negishi coupling between 3-bromofuran and an organozinc reagent derived from an iodoalanine derivative for the synthesis of a 3-(3-furyl)alanine derivative, and a judicious choice of reaction conditions to overcome the conformational constraints placed by converting a linear peptide into the corresponding macrocycle." @default.
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- W2986435102 date "2019-11-14" @default.
- W2986435102 modified "2023-09-26" @default.
- W2986435102 title "Total Synthesis of Endolides A and B" @default.
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- W2986435102 doi "https://doi.org/10.1055/s-0037-1610736" @default.
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