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- W2069489025 endingPage "8058" @default.
- W2069489025 startingPage "8052" @default.
- W2069489025 abstract "An enantiomerically and diastereomerically pure route has been developed for the first asymmetric synthesis of (1S,2R,3R,5R,7aR)- and (1S,2R,3R,5S,7aR)-1,2-dihydroxy-3,5-dihydroxymethylpyrrolizidine, hyacinthacine B1 and B2, featuring efficient and stereodefined elaboration via the asymmetric dihydroxylation (AD) of the functionalized homochiral pyrrolidine derivative prepared from (S)-(−)-2-pyrrolidone-5-carboxylic acid." @default.
- W2069489025 created "2016-06-24" @default.
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- W2069489025 date "2008-08-01" @default.
- W2069489025 modified "2023-09-27" @default.
- W2069489025 title "First asymmetric synthesis of pyrrolizidine alkaloids, (+)-hyacinthacine B1 and (+)-B2" @default.
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- W2069489025 doi "https://doi.org/10.1016/j.tet.2008.06.078" @default.
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