The demand for better medicines, advances in technology, and protecting the food we consume all have one tool in common that has overwhelmingly improved the ability of chemists to placate these demands: Heck, Negishi, and Suzuki coupling reactions. This issue covers TCI’s chemistry expertise in palladium catalysts for cross-coupling, trifluoroborate salts for Suzuki-Miyaura reactions, oxidative cross-coupling trifluoromethylation reagents via oxidative cross coupling, and how enol tosylate for cross-coupling reaction can help your research.
Palladium Catalysts for Cross-coupling Reaction
Organopalladium complexes generally show lower reactivity compared to those of organonickel complexes. However, their chemical stability against oxidation make organopalladium complexes easier to handle and are the preferred reagents for cross-coupling reactions. See how TCI’s tetrakis(triphenylphosphine)palladium(0) [T1350], widely used as a catalyst for palladium-catalyzed coupling reactions, can help make your reactions more stable and safe.
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