Dimeric or Mononuclear Cyclopalladated (Pre)catalysts: Which is More Active in the Suzuki–Miyaura Reaction?

The high catalytic activity of commercially available dimeric C,N-palladacycle based on N,N-dimethylbenzylamine in the Suzuki–Miyaura cross-coupling between aryl bromides and phenylboronic acid under mild reaction conditions is demonstrated.

Authors

Publication Details

Journal
INEOS OPEN
Published
2025-04-29
DOI
https://doi.org/10.32931/io2517a
Citations
1
Primary Topic
Catalytic Cross-Coupling Reactions
Type
article
Field-Weighted Citation Impact
0.94
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article

Dimeric or Mononuclear Cyclopalladated (Pre)catalysts: Which is More Active in the Suzuki–Miyaura Reaction?

Olga N. Gorunova, К. А. Кочетков, M. P. Timerkaeva
1 citations
INEOS OPEN
Catalytic Cross-Coupling Reactions
0.94
article

Dimeric or Mononuclear Cyclopalladated (Pre)catalysts: Which is More Active in the Suzuki–Miyaura Reaction?

Olga N. Gorunova, К. А. Кочетков, M. P. Timerkaeva
article en
1 citations

Abstract

The high catalytic activity of commercially available dimeric C,N-palladacycle based on N,N-dimethylbenzylamine in the Suzuki–Miyaura cross-coupling between aryl bromides and phenylboronic acid under mild reaction conditions is demonstrated.

INEOS OPENVol. 8(1-3)
Openalex Percentile: Top 23%
Catalytic Cross-Coupling Reactions
0.94
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Dimeric or Mononuclear Cyclopalladated (Pre)catalysts: Which is More Active in the Suzuki–Miyaura Reaction? — Olga N. Gorunova, К. А. Кочетков, et al. · INEOS OPEN (2025) | TGRS Research Map | TGRS