Abstract
Bulking up: The thermal barrier to rearrangement of a vicdisulfoxide is significantly increased through steric buttressing about the (O)S-S(O) bond. Whereas the title compounds represent the most thermally stable vicdisulfoxides known to date, they also undergo a novel photomediated epimerization at room temperature (see scheme). © 2009 Wiley-VCH Verlag GmbH & Co. KGaA.
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Grainger, R. S., Patel, B., & Kariuki, B. M. (2009). 2,7-Di-tert-butylnaphtho[1,8-cd][1,2]dithiole 1,2-dioxides: thermally stable, photochemically active vic-disulfoxides. Angewandte Chemie - International Edition, 48(26), 4832–4835. https://doi.org/10.1002/anie.200901788
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