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- W2947461877 abstract "Synthesis of the C2-symmetric, non-adjacent bis(tetrahydrofuran) core of squamostanin C in seven steps and 24% overall yield from (R,R)-1,5-hexadiene-3,4-diol is reported. Silicon-tethered, size-selective triple ring-closing metathesis of an acyclic hexaene is employed for assembly of the central 1,4-diol unit and concurrent chain extension via lactone formation. Stereoselective construction of both tetrahydrofuran rings is achieved in one step through the use of two-directional Mukaiyama aerobic alkenol cyclization." @default.
- W2947461877 created "2019-06-07" @default.
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- W2947461877 date "2019-07-01" @default.
- W2947461877 modified "2023-09-27" @default.
- W2947461877 title "Synthesis of the non-adjacent bis(tetrahydrofuran) core of squamostanin C by silicon-tethered, size-selective triple ring-closing metathesis" @default.
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- W2947461877 doi "https://doi.org/10.1016/j.tetlet.2019.05.064" @default.
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