MnFe2O4 Nanoparticles‐Catalyzed C3‐Alkylation of Indoles with Benzyl Alcohols under Solvent‐Free Conditions DOI Creative Commons
Ha V. Le, Huy X. Le, Vy T. Nguyen

et al.

ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(33)

Published: Aug. 28, 2024

Abstract Herein, we present an efficient, one‐pot reaction for accessing 3‐benzylated indoles via the coupling of benzyl alcohols with under heterogeneous catalysis by manganese ferrite (MnFe 2 O 4 ) nanoparticles. Notably, this reaction, first time, employs MnFe nanoparticles prepared using a simple grinding method. The high compatibility enables broad substrate scope and regioselectivity. Moreover, approach offers several attractive highlights including use recyclable oxide catalyst green cost‐effective alkylating reagents solvent‐free conditions.

Language: Английский

MnFe2O4 Nanoparticles‐Catalyzed C3‐Alkylation of Indoles with Benzyl Alcohols under Solvent‐Free Conditions DOI Creative Commons
Ha V. Le, Huy X. Le, Vy T. Nguyen

et al.

ChemistrySelect, Journal Year: 2024, Volume and Issue: 9(33)

Published: Aug. 28, 2024

Abstract Herein, we present an efficient, one‐pot reaction for accessing 3‐benzylated indoles via the coupling of benzyl alcohols with under heterogeneous catalysis by manganese ferrite (MnFe 2 O 4 ) nanoparticles. Notably, this reaction, first time, employs MnFe nanoparticles prepared using a simple grinding method. The high compatibility enables broad substrate scope and regioselectivity. Moreover, approach offers several attractive highlights including use recyclable oxide catalyst green cost‐effective alkylating reagents solvent‐free conditions.

Language: Английский

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