Posts tagged: Shauna Paradine

Shauna Paradine, ’08

Altermann, S. M., Richardson, R. D., Paradine, S. M., French, A. N., Page, T. K., Schmidt, R. K., et al. (2008). Catalytic Enantioselective Alpha-Oxysulfonylation of Ketones Mediated by Iodoarenes. European Journal of Organic Chemistry(31), 5315-5328.

Abstract: The alpha-oxysulfonylation of ketones catalysed by enantio enriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity. We believe this to be the first report of an enantioselective organocatalytic reaction involving hypervalent iodine reagents which should open up a new field for enantioselective organocatalysis of oxidation reactions. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008)

Shauna Paradine, ’08

Richardson, R. D., Page, T. K., Altermann, S., Paradine, S. M., French, A. N., & Wirth, T. (2007). Enantioselective Alpha-Oxytosylation of Ketones Catalysed by Iodoarenes. Synlett(4), 538-542.

Abstract: The alpha-oxytosylation of ketones catalysed by enantioenriched iodoarenes using mCPBA as stoichiometric oxidant is reported to give useful synthetic intermediates in good yield and modest enantioselectivity. We believe this to be the first report of an enantioselective catalytic reaction involving hypervalent iodine reagents which should open up a new field for enantioselective organocatalysis of oxidation reactions.

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