Palladium-tetraphosphine complex catalysed heck reaction of vinyl bromides with alkenes: A powerful access to conjugated dienes
M Lemhadri, A Battace, F Berthiol, T Zair, H Doucet…
Index: Lemhadri, Mhamed; Battace, Ahmed; Berthiol, Florian; Zair, Touriya; Doucet, Henri; Santelli, Maurice Synthesis, 2008 , # 7 p. 1142 - 1152
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Citation Number: 14
Abstract
Abstract A wide variety of 1, 3-dienes have been prepared by the Heck vinylation of vinyl bromides using [Pd (η 3-C 3 H 5) Cl] 2/cis, cis, cis-1, 2, 3, 4-tetrakis [(diphenylphosphino) methyl] cyclopentane (Tedicyp) as the catalyst precursor. Both α-and β-substituted vinyl bromides undergo the Heck reaction with functionalised alkenes such as acrylates, enones, styrenes or a vinyl sulfone, and also with nonfunctionalised alkenes such as dec-1-ene, ...
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