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Search for "oxidative difunctionalization" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Recent advances in oxidative radical difunctionalization of N-arylacrylamides enabled by carbon radical reagents

  • Jiangfei Chen,
  • Yi-Lin Qu,
  • Ming Yuan,
  • Xiang-Mei Wu,
  • Heng-Pei Jiang,
  • Ying Fu and
  • Shengrong Guo

Beilstein J. Org. Chem. 2025, 21, 1207–1271, doi:10.3762/bjoc.21.98

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  • been extensively investigated by researchers. Keywords: carbon radical reagents; intramolecular transformations; N-arylacrylamides; oxidative difunctionalization; radical reactions; Introduction Alkenes, as abundant and versatile feedstocks, have been widely employed in organic synthesis
  • to the formation of radical annulation species 59. Single-electron oxidation and deprotonation then take place, resulting in the final cyclized products 56a. N-Arylalkenes: α-carbonyl alkyl C(sp3)-centered radicals In 2014, Li’s group developed an oxidative difunctionalization of N-arylacrylamides
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Review
Published 24 Jun 2025

Tandem copper and photoredox catalysis in photocatalytic alkene difunctionalization reactions

  • Nicholas L. Reed,
  • Madeline I. Herman,
  • Vladimir P. Miltchev and
  • Tehshik P. Yoon

Beilstein J. Org. Chem. 2019, 15, 351–356, doi:10.3762/bjoc.15.30

Graphical Abstract
  • ) complex. We describe herein the results of this investigation, which has led to the identification of a tandem photoredox copper(II) catalytic system for the net-oxidative difunctionalization of alkenes. Results and Discussion A range of mild oxidants can oxidize copper(I) to copper(II), and the use of
  • oxidant in a stoichiometric fashion. Thus, it seems clear that the role of the Ag(I) additive in this reaction is to re-oxidize Cu(I) to Cu(II), and that the Cu(II) salt in this transformation is indeed a cocatalyst for the oxidative difunctionalization of styrenes. Efforts to render this transformation
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Letter
Published 05 Feb 2019
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