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- W2078114311 endingPage "7419" @default.
- W2078114311 startingPage "7392" @default.
- W2078114311 abstract "Aiming at a convergent total synthesis of ciguatoxin CTX1B, its EF-ring segment has been synthesized. During the synthesis, a novel method for the construction of branched ethers, based on regioselective reduction of γ-alkoxy β,γ-unsaturated α-silyloxy nitriles with borontrifluoride etherate and trialkyl silane or tributyltin hydride, has been developed. Combination use of the method and ring-closing olefin metathesis successfully provided medium-sized cyclic ethers. Efficient site-selective reduction of vinyl epoxides into homoallyl alcohols has also been developed." @default.
- W2078114311 created "2016-06-24" @default.
- W2078114311 creator A5037908115 @default.
- W2078114311 creator A5043346174 @default.
- W2078114311 creator A5048014569 @default.
- W2078114311 creator A5050382042 @default.
- W2078114311 creator A5062840062 @default.
- W2078114311 creator A5082994068 @default.
- W2078114311 date "2005-08-01" @default.
- W2078114311 modified "2023-10-09" @default.
- W2078114311 title "Synthesis of the EF-ring segment of ciguatoxin CTX1B based on novel regioselective reduction of unsaturated cyanohydrins and ring-closing olefin metathesis" @default.
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