Rodrigues Fábio M S, Kucmierczyk Peter K, Pineiro Marta, Jackstell Ralf, Franke Robert, Pereira Mariette M, Beller Matthias
CQC, Departamento de Química, Universidade de Coimbra, Rua Larga, 3004-535, Coimbra, Portugal.
Leibniz-Institut für Katalyse e.V. an der, Universität Rostock, Albert-Einstein-Str. 29a, 18059, Rostock, Germany.
ChemSusChem. 2018 Jul 20;11(14):2310-2314. doi: 10.1002/cssc.201800488. Epub 2018 Jul 2.
An active and selective dual catalytic system to promote domino hydroformylation-reduction reactions is described. Apart from terminal, di- and trisubstituted olefins, for the first time the less active internal C-C double bond of tetrasubstituted alkenes can also be utilized. As an example, 2,3-dimethylbut-2-ene is converted into the corresponding n-alcohol with high yield (90 %) as well as regio- and chemoselectivity (>97 %). Key for this development is the use of a combination of Rh complexes with bulky monophosphite ligands and the Ru-based Shvo's complex. A variety of aromatic and aliphatic alkenes can be directly used to obtain mainly linear alcohols.
描述了一种用于促进多米诺骨牌式氢甲酰化-还原反应的活性和选择性双催化体系。除了末端、二取代和三取代烯烃外,首次还可以利用四取代烯烃活性较低的内部碳-碳双键。例如,2,3-二甲基-2-丁烯以高产率(90%)以及区域和化学选择性(>97%)转化为相应的正醇。这一进展的关键是使用铑配合物与大位阻单膦配体以及钌基什沃配合物的组合。多种芳香族和脂肪族烯烃可直接用于主要获得线性醇。