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- W2024365087 abstract "(6R,7S,8aR)- and (6S,7R,8aR)-8a-tert-butyldimethylsilyloxymethyl-6,7-dihydroxy-indolizidin-3-ones 14 and 15 were synthesized from bicyclic silyloxypyrrole 2 by the selective formation of a quaternary stereogenic centre and a ring-closing metathesis as the main steps. They were converted into new polyhydroxyindolizidines 20 and 21 with high diastereoselectivity." @default.
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- W2024365087 date "2006-01-01" @default.
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- W2024365087 title "Creation of quaternary stereocentres: synthesis of new polyhydroxylated indolizidines" @default.
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- W2024365087 doi "https://doi.org/10.1016/j.tetasy.2005.11.017" @default.
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