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Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy.

European journal of organic chemistry (2014-05-16)
Jai K Chavda, Panayiotis A Procopiou, Peter N Horton, Simon J Coles, Michael J Porter
RESUMEN

The tricyclic BCD substructure of the marine natural product nakadomarin A has been synthesised. The strategy utilised a key carbon-carbon bond-forming reaction between a furan and an

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Furan-3-methanol, 99%