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Synthesis of a Deuterated Standard for the Quantification of 2-Arachidonoylglycerol in Caenorhabditis elegans
Published on: September 21, 2019
Total Synthesis of (+)-Strongylophorines 2 and 9
Dattatraya H Dethe1, Susanta Kumar Sau1
1Department of Chemistry , Indian Institute of Technology , Kanpur , Uttar Pradesh 208016 , India.
Abstract:
The first enantioselective total syntheses of highly complex hexacyclic meroterpenoids STR-2 and -9 (strongylophorine (STR)) are reported. Key elements of the synthetic route include the use of Robinson-type annulation reaction to construct the tricyclic terpenoid building block and a highly efficient PIDA-mediated 1,3-diaxial sp3 C-H activation to incorporate the requisite δ-lactone moiety. This route also enables the determination of absolute configuration of the synthesized natural products.
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