A formal [2π+2σ] cycloaddition between electron-rich allenes and bicyclobutanes (BCBs), under a gold-catalyzed regime, is reported. A dual gold activation mechanism was revealed through kinetic studies and further supported by detailed DFT analysis, introducing intriguing paradigms into the dual activation strategy of homogeneous Au catalysis. This protocol enables the synthesis of a broad array of densely functionalized bicyclohexanes (32 examples) in high yields (up to 93%) with complete regioselectivity and stereoselectivity.
Giovanelli, R., Gallorini, G., Huang, Y., Brunetti, A., Nikopoulos, K.D., Monari, M., et al. (2025). Dual [Au(I)]-Catalysis in Regioselective Cycloaddition of Bicy-clo[1.1.0]butanes with Allenes. ACS CATALYSIS, 17(15), 15698-15705 [10.1021/acscatal.5c03898].
Dual [Au(I)]-Catalysis in Regioselective Cycloaddition of Bicy-clo[1.1.0]butanes with Allenes
Riccardo Giovanelli;Giulio Gallorini;Yuhao Huang;Andrea Brunetti;Magda Monari;Giulio Bertuzzi
;Marco Bandini
2025
Abstract
A formal [2π+2σ] cycloaddition between electron-rich allenes and bicyclobutanes (BCBs), under a gold-catalyzed regime, is reported. A dual gold activation mechanism was revealed through kinetic studies and further supported by detailed DFT analysis, introducing intriguing paradigms into the dual activation strategy of homogeneous Au catalysis. This protocol enables the synthesis of a broad array of densely functionalized bicyclohexanes (32 examples) in high yields (up to 93%) with complete regioselectivity and stereoselectivity.| File | Dimensione | Formato | |
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ACS_catalysis-25 (Au-BCB).pdf
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Gold catalyzed [1.1.0] BCB Supp Info (revision).docx
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