Abstract
Molecular flasks of self-assembled M6L4 nanocages promote the [2+2] photodimerization of olefins in a surprisingly efficient fashion. Thus, the dimerization of acenaphthylenes and naphthoquinones quantitatively proceeded in the cavity with remarkable rate acceleration and perfect regio- and stereo-control (> 98%, see scheme).
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Yoshizawa, M., Takeyama, Y., Kusukawa, T., & Fujita, M. (2002). Cavity-directed, highly stereoselective [2+2] photodimerization of olefins within self-assembled coordination cages. Angewandte Chemie - International Edition, 41(8), 1347–1349. https://doi.org/10.1002/1521-3773(20020415)41:8<1347::AID-ANIE1347>3.0.CO;2-X
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