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- W2951166105 abstract "Radical-mediated opening of a trisubstituted epoxy alcohol using cp2TiCl was followed by diastereoselective reduction of the resulting product with a centrally located methylene group, flanked on both sides by two chiral hydroxyl-bearing carbons, to build all the three chiral centers of (+)-prelactone B 1 in their desired stereochemistries leading to the total synthesis of the molecule." @default.
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- W2951166105 date "2003-03-01" @default.
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- W2951166105 title "Synthesis of (+)-prelactone B" @default.
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- W2951166105 doi "https://doi.org/10.1016/s0040-4039(03)00326-5" @default.
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