Abstract
The choice is yours: The first total synthesis of the antioxidant carotenoid synechoxanthin was achieved through a novel iterative cross-coupling approach in which the polarity of the bifunctional building blocks is reversed to match the preferred polarity for C-C bond formation (see scheme). The convergent, stereocontrolled, and flexible nature of this synthesis enables systematic studies of the biological activities of this natural product. © 2011 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.
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Fujii, S., Chang, S. Y., & Burke, M. D. (2011). Total synthesis of synechoxanthin through iterative cross-coupling. Angewandte Chemie - International Edition, 50(34), 7862–7864. https://doi.org/10.1002/anie.201102688
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