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- W2032275823 abstract "Saturated and unsaturated seven- and eight-membered cyclic ethers of the type found in the brevetoxins and ciguatoxins have been prepared in enantiomerically pure form in 10 steps from a readily available chiral pool material. The key steps in this sequence are ring-closing metathesis of allylic ethers, and subsequent elaboration of the cyclic allylic ether products by stereoselective epoxide formation and ring-opening." @default.
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- W2032275823 date "1998-11-01" @default.
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- W2032275823 title "Synthesis of medium-sized cyclic allylic ethers by ring-closing metathesis and subsequent elaboration to sub-units found in the brevetoxins and ciguatoxins" @default.
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- W2032275823 doi "https://doi.org/10.1016/s0040-4039(98)01825-5" @default.
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