Abstract
Background: The dihydroazulene (DHA)/vinylheptafulvene (VHF) system (with two cyano groups at C1) functions as a photo-/thermoswitch. Direct ionic bromination of DHA has previously furnished a regioselective route to a 7,8-dibromide, which by elimination was converted to a 7-bromo-substituted DHA. This compound has served as a central building block for functionalization of the DHA by palladium-catalyzed cross-coupling reactions. The current work explores another bromination protocol for achieving the isomeric 3-bromo-DHA and also explores the outcome of additional bromination of this compound as well as of the known 7-bromo-DHA. © 2012 Mazzanti et al.
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Mazzanti, V., Cacciarini, M., Broman, S. L., Parker, C. R., Schau-Magnussen, M., Bond, A. D., & Nielsen, M. B. (2012). On the bromination of the dihydroazulene/vinylheptafulvene photo-/thermoswitch. Beilstein Journal of Organic Chemistry, 8, 958–966. https://doi.org/10.3762/bjoc.8.108
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