2022
DOI: 10.1039/d2ob00620k
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Total synthesis of (±)-mersicarpine following a 6-exo-trig radical cyclization

Abstract: Described is a total synthesis of racemic mersicarpine from diethyl 4-oxopimelate. The synthetic route takes advantage of a 2-indolyl radical cyclization to construct the pyrido[1,2-a]indole scaffold bearing the all-carbon quaternary...

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“…Our laboratory is currently investigating the potential of this promising intramolecular cyclization reaction to synthesize valuable scaffolds for Aspidosperma alkaloids. 19 …”
mentioning
confidence: 99%
“…Our laboratory is currently investigating the potential of this promising intramolecular cyclization reaction to synthesize valuable scaffolds for Aspidosperma alkaloids. 19 …”
mentioning
confidence: 99%