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- W3100588207 abstract "Substances containing a spirooxindole framework display important biological activities. Natural alkaloid capparine A [(S)-(−)-1] has an anti-inflammatory effect. In the present study, attention has been paid to the first total synthesis of natural capparine A [(S)-(−)-1]. Racemic capparine A [(±)-1] was synthesized by bromospirocyclization of 6-methoxy-1-Boc-brassinin with water, followed by oxidation of obtained spirobrassinol derivatives and removal of the Boc group. Synthesized racemic capparine A [(±)-1] was enantioresolved by derivatization with (1R,2S,5R)-menthyl chloroformate, chromatographic separation of diastereoisomers and the cleavage of the chiral auxiliary using sodium methoxide. Screening of anti-proliferative activity against human cancer cells revealed no anti-proliferative activity of the capparine A [(S)-(−)-1]." @default.
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- W3100588207 date "2021-01-01" @default.
- W3100588207 modified "2023-09-26" @default.
- W3100588207 title "The first synthesis of natural alkaloid capparine A" @default.
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- W3100588207 doi "https://doi.org/10.1016/j.tet.2020.131772" @default.
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