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- W2011591036 endingPage "3597" @default.
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- W2011591036 abstract "In an effort to access biologically important scaffolds, a concise branch-selective synthesis of C3 tertiary oxindoles by Cu(I)-catalyzed aryl amidation and 2,2-dimethyl indene by Pd(0)-catalyzed Heck cyclization has been accomplished from acyclic reverse-prenylated intermediates. Oxindole C3-enolate generation using NaH followed by alkylation in the presence of appropriate electrophiles provides a novel route to quaternary C3 reverse-prenylated oxindoles." @default.
- W2011591036 created "2016-06-24" @default.
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- W2011591036 date "2010-07-27" @default.
- W2011591036 modified "2023-10-07" @default.
- W2011591036 title "Branch-Selective Synthesis of Oxindole and Indene Scaffolds: Transition Metal-Controlled Intramolecular Aryl Amidation Leading to C3 Reverse-Prenylated Oxindoles" @default.
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- W2011591036 doi "https://doi.org/10.1021/ol1012372" @default.
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