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Tricyclohexylphosphonium tetrafluoroborate is used with ruthenium (1,5-cyclooctadiene)ruthenium dimer to catalyze the dehydrogenative coupling of alcohols and amines to form amide bonds. It is also used in suzuki reaction.
Air-stable replacement for tricyclohexylphosphine in various Pd-catalyzed coupling reactions. Used in conjunction with Bis(1,5-cyclooctadiene)nickel(0), 39234 in Ni(0)-catalyzed Suzuki-Miyaura-type coupling of alkenyl phosphates with arylboronic acids and esters to give 1,1-diarylalkenes: Chem. Commun., 4137 (2006). See also Tri-tert-butylphosphonium tetrafluoroborate, L19752.
Hayashi, S.; Kojima, Y.; Koizumi, T. Highly regioselective Pd/C-catalyzed direct arylation toward thiophene-based π-conjugated polymers. Polym. Chem. 2015, 6 (6), 881-885.
Ueda, Y.; Tsuji, H.; Tanaka, H.; Nakamura, E. Synthesis, Crystal Packing, and Ambipolar Carrier Transport Property of Twisted Dibenzo [g, p] chrysenes. Chem. Asian J. 2014, 9 (6), 1623-1628.
Hazard Statements: H315-H319-H335
Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
Precautionary Statements: P280g-P305+P351+P338
Wear protective gloves. IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing.