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Synthesis 2017; 49(07): 1538-1546
DOI: 10.1055/s-0036-1588113
DOI: 10.1055/s-0036-1588113
paper
Enantioselective Catalytic One-Pot Synthesis of Functionalized Methyleneindanes and Methylindenes via a Michael/Conia-Ene Sequence
Weitere Informationen
Publikationsverlauf
Received: 09. November 2016
Accepted after revision: 11. November 2016
Publikationsdatum:
06. Dezember 2016 (online)
Abstract
An enantioselective one-pot Michael addition/Conia-ene reaction sequence catalyzed by the combination of a squaramide and indium(III) triflate has been developed. Employing 2-ethynyl-β-nitrostyrenes and 1,3-dicarbonyl compounds as substrates, the functionalized methyleneindanes and methylindenes are obtained in good to excellent enantiomeric excesses. For the indane/indene conversion a concerted fragmentation is proposed.
Supporting Information
- Supporting information for this article is available online at http://dx.doi.org/10.1055/s-0036-1588113.
- Supporting Information
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For selected indane examples, see:
For selected indene examples, see:
For recent indane syntheses undertaken by our group, see: