Highly symmetric all-metal aromatic Pd3+ complexes can catalyze the cycloisomerization of terminal 1,6-enynes and internal dienynes under mild conditions. Modification of substrates dictates the mechanism and steers the reaction toward different polycyclic frameworks, enabling the development of complex cascades. The reactivity of Pd(4/3) complexes is complementary to that of mononuclear Pd(0) and Pd(II) ones.
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes / Lanzi, Matteo; Cañeque, Tatiana; Marchiò, Luciano; Maggi, Raimondo; Bigi, Franca; Malacria, Max; Maestri, Giovanni. - In: ACS CATALYSIS. - ISSN 2155-5435. - 8:(2018), pp. 144-147. [10.1021/acscatal.7b03366]
Alternative Routes to Tricyclic Cyclohexenes with Trinuclear Palladium Complexes
LANZI, MATTEO;Marchiò, Luciano;Maggi, Raimondo;Bigi, Franca;Maestri, Giovanni
2018-01-01
Abstract
Highly symmetric all-metal aromatic Pd3+ complexes can catalyze the cycloisomerization of terminal 1,6-enynes and internal dienynes under mild conditions. Modification of substrates dictates the mechanism and steers the reaction toward different polycyclic frameworks, enabling the development of complex cascades. The reactivity of Pd(4/3) complexes is complementary to that of mononuclear Pd(0) and Pd(II) ones.| File | Dimensione | Formato | |
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