4.8 Article

Dual Gold/Silver Catalysis: Indolizines from 2-Substituted Pyridine Derivatives via a Tandem C(sp(3))-H Alkynylation/Iminoauration

Journal

ORGANIC LETTERS
Volume 23, Issue 24, Pages 9480-9484

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.1c03667

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Funding

  1. CSC (China Scholarship Council)

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A dual gold/silver-catalyzed cascade reaction was described for the synthesis of indolizines, yielding compounds with diverse functionalities in good to excellent yield. Furthermore, a gram-scale reaction was efficiently conducted in this study.
A dual gold/silver-catalyzed cascade C(sp(3))-H alkynylation/iminoauration of 2-substituted pyridines with hyper-valent iodine(III) reagents for the synthesis of indolizines is described. This novel reaction involves the formation of an alkynyl Au(III) species, a dual gold/silver-catalyzed C(sp(3))-H functionalization, and a subsequent iminoauration process. A number of indolizines bearing diverse functionalities were prepared in good to excellent yield. Furthermore, a gram-scale reaction was efficiently conducted.

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