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• W2057385918 endingPage "3217" @default.
• W2057385918 startingPage "3214" @default.
• W2057385918 abstract "Regiocontrolled oxidative cyclizations of 3-substituted indoles are described herein. Specifically, it is shown that the installation of a chloride at C2 alters the inherent propensity for cyclization at the 2-position of indole so as to favor the 4-position, enabling the construction of the unique framework found in most welwitindolinone alkaloids. The chloride functions here as more than a blocking group, as it also provides ready access to the corresponding oxindole." @default.
• W2057385918 created "2016-06-24" @default.
• W2057385918 creator A5040734473 @default.
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• W2057385918 date "2011-05-26" @default.
• W2057385918 modified "2023-10-10" @default.
• W2057385918 title "Directed Oxidative Cyclizations to C2- or C4-Positions of Indole: Efficient Construction of the Bicyclo[4.3.1]Decane Core of Welwitindolinones" @default.
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• W2057385918 doi "https://doi.org/10.1021/ol201122f" @default.
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