Decandrinin (1), an unprecedented C9-spiro-fused 7,8-seco-ent-abietane, was obtained from the bark of an Indian mangrove, Ceriops decandra, collected in the estuary of Godavari, Andhra Pradesh. The constitution and the relative configuration of 1 were determined by HRMS (ESI) and extensive NMR investigations, and the absolute configuration by circular dichroism (CD) and optical-rotatory dispersion (ORD) spectroscopy in combination with quantum-chemical calculations. Decandrinin is the first 7,8- seco-ent-abietane. © 2014 Wang et al; licensee Beilstein-Institut.
CITATION STYLE
Wang, H., Li, M. Y., Katele, F. Z., Satyanandamurty, T., Wu, J., & Bringmann, G. (2014). Decandrinin, an unprecedented C9-spiro-fused 7,8-seco-ent-abietane from the Godavari mangrove Ceriops decandra. Beilstein Journal of Organic Chemistry, 10, 276–281. https://doi.org/10.3762/bjoc.10.23
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