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April 18, 2026Organic Letters2 citations

Photoactivation of Electron Donor–Acceptor Complexes via Quinolinium Salts and 4-Carboxamide-1,4-dihydropyridines: Synthesis of N -Heteroaryl-2-carboxamides

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PYPengpeng YinKMKay Thwe MoeYLYun-Xuan Luo

Key Points

  • The research aims to synthesize N-heteroaryl-2-carboxamides using electron donor-acceptor complexes with quinolinium salts.
  • Utilized Lewis acid coordination to enhance the reduction potential of quinoline.
  • Established electron donor-acceptor complex with Hantzsch ester donors.
  • Conducted the reaction under mild aerobic conditions without external oxidants.
  • Achieved target C–H amidation through initial single-electron transfer.
  • Generated singlet oxygen to mediate the subsequent oxygenation process.
  • Eliminated the need for photosensitizers and metal catalysts.

Abstract

By leveraging Lewis acid coordination to increase the reduction potential of quinoline to facilitate the formation of an electron donor–acceptor (EDA) complex with Hantzsch ester donors, this work establishes a dual function of the quinolinium salts. This dual function involves the initial single-electron transfer (SET) triggering the target C–H amidation and energy transfer for the generation of singlet oxygen to mediate the subsequent oxygenation process. Consequently, this protocol achieves the transformation under mild aerobic conditions, eliminating the requirement for external photosensitizers, metal catalysts, or strong oxidants.

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Cite This Study

Yin et al. (2026) studied this question.

synapsesocial.com/papers/69e320e740886becb654008bhttps://doi.org/10.1021/acs.orglett.6c00635
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