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Updated: Feb 15, 2026

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
Published on: April 19, 2019
Synthesis of Quinolizinium-Type Heteroaromatics via a Carbene Intermediate
Feng Li1, Jihee Cho1, Shenpeng Tan1
1College of Pharmacy, Seoul National University , 1 Gwanak-ro, Gwanak-gu, Seoul 08826, Korea.
Abstract:
An efficient synthesis of quinolizinium-type heteroaromatics by Pt(II)-catalyzed cyclization of 2-arylpyridine propargyl alcohol has been developed. The presence of a protic acid is crucial for the success of the reaction. Mechanistic studies disclosed that the reaction proceeds via a platinum-carbene intermediate. Additionally, the fluorescence properties of the synthesized heteroaromatics were investigated to provide perspectives for potential applications.
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