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- W2295801657 abstract "The asymmetric 1,6-conjugate addition of arylboronic acids to natural securinine under rhodium(I) catalysis displays a very high regioselectivity, along with a remarkable diastereoselectivity (>99:1) and high yields. The in vitro cytotoxicity of the resulting securinine analogues was assayed against HCT-116 colon cancer cells, giving a new insight into the structure–activity relationship of securinine." @default.
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- W2295801657 date "2016-01-21" @default.
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- W2295801657 title "Highly Diastereoselective 1,6-Conjugate Addition of Arylboronic Acids to Securinine" @default.
- W2295801657 doi "https://doi.org/10.1055/s-0035-1561340" @default.
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