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Cobaltaelectro-Catalyzed C-H Activation for Central and Axial Double Enantio-Induction.
von Münchow, Tristan; Liu, Yi-Ru; Parmar, Rahul; Peters, Sven Erik; Trienes, Sven; Ackermann, Lutz.
Affiliation
  • von Münchow T; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
  • Liu YR; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
  • Parmar R; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
  • Peters SE; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
  • Trienes S; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
  • Ackermann L; Institut für Organische und Biomolekulare Chemie, Wöhler-Research Institute for Sustainable Chemistry (WISCh), Georg-August-Universität Göttingen, Tammannstraße 2, 37077, Göttingen, Germany.
Angew Chem Int Ed Engl ; 63(31): e202405423, 2024 Jul 29.
Article in En | MEDLINE | ID: mdl-38758011
ABSTRACT
In recent years, enantioselective electrocatalysis has surfaced as an increasingly-effective platform for sustainable molecular synthesis. Despite indisputable progress, strategies that allow the control of two distinct stereogenic elements with high selectivity remain elusive. In contrast, we, herein, describe electrochemical cobalt-catalyzed C-H activations that enable the installation of chiral stereogenic centers along with a chiral axis with high levels of enantio- and diastereoselectivities. The developed electrocatalysis strategy allowed for C-H/N-H activations/annulations with cyclic and non-cyclic alkenes providing expedient access to various central as well as atropo-chiral dihydroisoquinolinones paired to the valuable hydrogen evolution reaction. Studies on the atropo-stability of the obtained compounds demonstrated that the exceedingly mild conditions ensured by the electrocatalytic process were key for the achieved high stereoselectivities.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Alemania

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Angew Chem Int Ed Engl Year: 2024 Document type: Article Affiliation country: Alemania Country of publication: Alemania