Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step

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Abstract

(Chemical Equation Presented) The combined approach of C-H activation and a Cope rearrangement catalyzed by a rhodium catalyst [Rh2(R-dosp) 4] (dosp = (N-dodecylbenzenesulfonyl)prolinate) is shown to be a very effective method for the construction of the three stereogenic centers (marked in red, see scheme) present in the diterpene erogorgiaene (1). © 2005 Wiley-VCH Verlag GmbH & Co. KGaA.

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Davies, H. M. L., & Walji, A. M. (2005). Direct synthesis of (+)-erogorgiaene through a kinetic enantiodifferentiating step. Angewandte Chemie - International Edition, 44(11), 1733–1735. https://doi.org/10.1002/anie.200462227

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