JOURNAL ARTICLE

Metal-Free Synthesis of Functionalized Indolizines via a Cascade Michael/SN2/Aromatization Reaction of 2-Alkylazaarene Derivatives with Bromonitroolefins

Kangbiao ChenRui ZhouGaofeng ZhuLei TangLu HuangQing He

Year: 2024 Journal:   ACS Omega Vol: 9 (50)Pages: 49980-49985   Publisher: American Chemical Society

Abstract

A transition metal-free domino Michael/SN2/aromatization annulation of 2-pyridylacetates with bromonitroolefins has been developed. A wide range of substrates containing various substituted groups was compatible with the present methodology and afforded functionalized indolizines with moderate to excellent yield (up to 99% yield). In addition, the potential practicality of the method stood out through scale-up reactions and further transformations to other valuable compounds. In our view, this study is an essential complement for the rapid construction of indolizine derivatives through a metal-free strategy.

Keywords:
Aromatization Indolizine Michael reaction Yield (engineering) Cascade reaction Chemistry Annulation Domino Combinatorial chemistry SN2 reaction Organic chemistry Materials science Catalysis

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