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- W4385855863 abstract "Abstract This article describes an effective and atom‐economical protocol to access a wide range of synthetically important functionalized indolizine derivatives. This transformation basically takes place through a Cu(II) catalyzed formal [3+2] annulation of 2‐pyridinyl substituted p ‐quinone methides with enaminones. This method displayed a good functional group tolerance and, was found to be effective for most of the enaminones and p ‐QMs, and the corresponding indolizines were obtained in moderate to good yields." @default.
- W4385855863 created "2023-08-17" @default.
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- W4385855863 date "2023-08-29" @default.
- W4385855863 modified "2023-10-18" @default.
- W4385855863 title "Cu(II)‐Catalyzed [3+2]‐Annulation of 2‐Pyridinyl‐substituted <i>p</i>‐Quinone Methides with Enaminones: Access to Functionalized Indolizine Derivatives" @default.
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- W4385855863 doi "https://doi.org/10.1002/adsc.202300634" @default.
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