Multicomponent Reactions of Pyridines To Give Ring‐Fused Pyridiniums: In Situ Activation Strategy Using 1, 2‐Dichloroethane as a Vinyl Equivalent. (30th November 2018)

• Record Type: Journal Article
• Authors: Wang, Zhishuo; Yin, Jiangliang; Zhou, Fulin; Liu, Yunqi; You, Jingsong
• Is Part Of: Angewandte Chemie. Volume 131:Number 1(2019)
• Page Start: 260
• Page End: 264
• Publication Date: 2018-11-30
• Subjects: C-H-Aktivierung -- Heterocyclen -- Mehrkomponenten-Reaktionen -- Rhodium -- Synthesemethoden; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.201812167
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Reported herein is a rhodium(III)‐catalyzed three‐component annulation reaction of simple pyridines, alkynes, and 1, 2‐dichloroethane (DCE), affording a streamlined pathway to diverse ring‐fused pyridiniums. DCE not only serves as a vinyl equivalent but also as an in situ activating agent for pyridine C2−H activation. A cationic five‐membered rhodacycle complex has been isolated and proposed as a possible intermediate. This strategy can be extended to other N‐containing heteroarenes for the synthesis of multiring‐fused pyridiniums. These multicomponent reactions exhibit excellent regioselectivity for 1, 3‐diynes, paving a path to the cascade cyclization of 3‐fluoropyridine or N ‐methylpyridin‐3‐amine with 1, 3‐diynes for the construction of brand‐new tricyclic‐fused pyrano‐ or hydropyridoquinolizinium salts. These ionic fluorophores have been investigated as potential biomarkers.