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Beilstein-Institut, Beilstein Journal of Organic Chemistry, (14), p. 2597-2601, 2018

DOI: 10.3762/bjoc.14.237

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Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation

This paper is made freely available by the publisher.
This paper is made freely available by the publisher.

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Abstract

A straightforward synthetic entry to functionalized hydrindane compounds based on a rapid assembly of the core nucleus by a Danheiser cycloaddition is reported. Valuable bicyclic building blocks containing the fused five and six-membered carbocyclic ring system can be achieved in only four steps from a simple acyclic β-keto ester.