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- W2950012306 abstract "Abstract Indoles undergo conjugate addition with α,β‐unsaturated ketones in the presence of a catalytic amount of antimony trichloride under refluxing condition to afford the corresponding Michael adduct in excellent yields. The substitution on the indole ring occurred exclusively at 3‐position without a trace of any N‐alkylated products." @default.
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- W2950012306 date "2007-07-01" @default.
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- W2950012306 title "Antimony Trichloride–Catalyzed Michael Addition of Indoles to the α,β‐Unsaturated Ketones" @default.
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- W2950012306 doi "https://doi.org/10.1080/00397910701410749" @default.
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