Abstract
Synthetic investigations towards the structurally complex and highly decorated framework of B-seco limonoid natural products by means of a [3,3]-sigmatropic rearrangement are described. Detailed model studies reveal, that an Ireland-Claisen rearrangement can be employed to construct the central C9-C10 bond thereby giving access to the B-seco limonoid scaffold. However, application of the developed strategy ended up failing in more complex and sterically demanding systems. © 2014 Bruss et al; licensee Beilstein-Institut.
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Bruss, H., Schuster, H., Martinez, R., Kaiser, M., Antonchick, A. P., & Waldmann, H. (2014). Synthesis of the B-seco limonoid core scaffold. Beilstein Journal of Organic Chemistry, 10, 194–208. https://doi.org/10.3762/bjoc.10.15
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