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- W2288474037 endingPage "1250" @default.
- W2288474037 startingPage "1241" @default.
- W2288474037 abstract "Potassium hydroxide-catalyzed hydrosilylation exhibits excellent activity and chemoselectivity for the reduction of cyclic imides under mild reaction conditions. The chemoselectivity of the reduction system may be readily tuned by changing the identity and stoichiometry of the hydrosilanes: a polymethylhydrosiloxane (PMHS)/potassium hydroxide reduction system resulted in the reduction of various cyclic imides to the corresponding ω-hydroxylactams in 70–94% yield, while the diphenylsilane (Ph2SiH2)/potassium hydroxide reduction system selectively afforded the aryl lactams in 33–95% yield. These catalytic protocols tolerate diverse functional groups and are easy to scale up." @default.
- W2288474037 created "2016-06-24" @default.
- W2288474037 creator A5026125673 @default.
- W2288474037 creator A5031510233 @default.
- W2288474037 creator A5039066496 @default.
- W2288474037 creator A5048649643 @default.
- W2288474037 creator A5063288717 @default.
- W2288474037 creator A5085959519 @default.
- W2288474037 date "2016-03-03" @default.
- W2288474037 modified "2023-10-14" @default.
- W2288474037 title "Potassium Hydroxide-Catalyzed Chemoselective Reduction of Cyclic Imides with Hydrosilanes: Synthesis of ω-Hydroxylactams and Lactams" @default.
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