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Royal Society of Chemistry, Organic and Biomolecular Chemistry, 25(21), p. 5245-5253, 2023

DOI: 10.1039/d3ob00545c

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Accessing spiropiperidines from dihydropyridones through tandem triflation–allylation and ring-closing metathesis (RCM)

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

We report an approach to build 2-spiropiperidine moieties starting from dihydropyridones through a tandem triflation–allylation reaction followed by ring-closing metathesis and then Pd-catalyzed functionalization.