Naturally occurring indole-3-carbinol and 3,3-diindolylmethane show bioactivity in a number of disparate disease areas, including cancer, prompting substantial synthetic analogue activity. We describe a new approach to highly functionalised derivatives that starts from allene gas and proceeds via the combination of a three-component Pd0-catalysed cascade with a one-pot, three-component carbophilic PtII cascade linked to a stereoselective acid-catalysed Mannich-Michael reaction that generates complex cyclopropyl diindolylmethanes which show selective activity against prostate cancer cell lines. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
CITATION STYLE
Groome, N. M., Elboray, E. E., Inman, M. W., Dondas, H. A., Phillips, R. M., Kilner, C., & Grigg, R. (2013). Carbophilic 3-component cascades: Access to complex bioactive cyclopropyl diindolylmethanes. Chemistry - A European Journal, 19(6), 2180–2184. https://doi.org/10.1002/chem.201202647
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