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- W2172918888 abstract "Following our recent total synthesis of the biologically potent natural products otteliones A and B in racemic form, we have now accomplished the total synthesis of both the enantiomers of otteliones A and B through an enantiodivergent strategy emanating from the readily available Diels-Alder adduct of cyclopentadiene and p-benzoquinone. These endeavors have led to the elucidation of the absolute configuration of naturally occurring otteliones A and B." @default.
- W2172918888 created "2016-06-24" @default.
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- W2172918888 date "2003-08-01" @default.
- W2172918888 modified "2023-10-18" @default.
- W2172918888 title "Enantioselective total syntheses of (+)- and (−)-ottelione A and (+)- and (−)-ottelione B. Absolute configuration of the novel, biologically active natural products" @default.
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- W2172918888 doi "https://doi.org/10.1016/s0040-4039(03)01643-5" @default.
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