Literature DB >> 25070407

Oxidative catalysis using the stoichiometric oxidant as a reagent: an efficient strategy for single-electron-transfer-induced tandem anion-radical reactions.

František Kafka1, Martin Holan, Denisa Hidasová, Radek Pohl, Ivana Císařová, Blanka Klepetářová, Ullrich Jahn.   

Abstract

Oxidative single-electron transfer-catalyzed tandem reactions consisting of a conjugate addition and a radical cyclization are reported, which incorporate the mandatory terminal oxidant as a functionality into the product.
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Keywords:  Michael addition; cyclization; domino reactions; electron transfer; radical reactions

Year:  2014        PMID: 25070407     DOI: 10.1002/anie.201403776

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  2 in total

Review 1.  Isolation and synthesis of cryptosanguinolentine (isocryptolepine), a naturally-occurring bioactive indoloquinoline alkaloid.

Authors:  Elida N Thobokholt; Enrique L Larghi; Andrea B J Bracca; Teodoro S Kaufman
Journal:  RSC Adv       Date:  2020-05-19       Impact factor: 4.036

2.  Chemoselective γ-Oxidation of β,γ-Unsaturated Amides with TEMPO.

Authors:  Sebastian Heindl; Margaux Riomet; Ján Matyasovsky; Miran Lemmerer; Nicolas Malzer; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2021-07-20       Impact factor: 15.336

  2 in total

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