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Rapid and Atom-Economical De Novo Access to Polysubstituted Quinolines via Sequential C-C Bond Cleavage and Reassembly.

Created on 25 Jun 2026

Authors

Yahui Zhang, Chao Pi, Yangjie Wu, Xiuling Cui

Published in

Organic letters. Jun 25, 2026. Epub Jun 25, 2026.

Abstract

Herein, we report a Cu(II), Rh(III) relay-catalyzed multicomponent reaction of easily available arylformylacetonitriles and alkynes, enabling the efficient de novo synthesis of polysubstituted quinolines via two steps in a "one-pot" manner. Various polysubstituted quinolines could be provided in up to 88% yields for 23 examples. The title products exhibit favorable fluorescence emission. Mechanistic studies suggest that unique domino two-C-C bond cleavage and the formation of multiple new bonds (five C-C bonds and one C-N bond) are involved in this process. This protocol features mild reaction conditions and is extremely simple and scalable. The luminescence of the products enhances their promising applications in functional materials.

PMID:
42348310
Bibliographic data and abstract were imported from PubMed on 25 Jun 2026.

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