Asymmetric synthesis of trans-dihydroarylfurans in a Friedel-Crafts/substitution domino reaction under squaramide catalysisElectronic supplementary information (ESI) available: Experimental procedure for synthesis of compounds 3 and X-ray data for compounds 3h and 3j. CCDC 902091 and 902092. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc38534a

Asymmetric synthesis of trans-dihydroarylfurans in a Friedel-Crafts/substitution domino reaction under squaramide catalysisElectronic supplementary information (ESI) available: Experimental procedure for synthesis of compounds 3 and X-ray data for compounds 3h and 3j. CCDC 902091 and 902092. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc38534a

Dihydroarylfuran skeletons are efficiently synthesized from ( Z )-bromonitroalkenes and naphthol derivatives in good yields and excellent enantioselectivities by using squaramide catalysis. Chiral trans -dihydroarylfuran derivatives can be efficiently synthesized from ( Z )-bromonitroalkenes and nap...

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Hauptverfasser: Jarava-Barrera, Carlos, Esteban, Francisco, Navarro-Ranninger, Carmen, Parra, Alejandro, Alemán, José
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Esteban, Francisco
Navarro-Ranninger, Carmen
Parra, Alejandro
Alemán, José
description Dihydroarylfuran skeletons are efficiently synthesized from ( Z )-bromonitroalkenes and naphthol derivatives in good yields and excellent enantioselectivities by using squaramide catalysis. Chiral trans -dihydroarylfuran derivatives can be efficiently synthesized from ( Z )-bromonitroalkenes and naphthol derivatives with good yields and excellent ee's by using squaramide catalysis.
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title Asymmetric synthesis of trans-dihydroarylfurans in a Friedel-Crafts/substitution domino reaction under squaramide catalysisElectronic supplementary information (ESI) available: Experimental procedure for synthesis of compounds 3 and X-ray data for compounds 3h and 3j. CCDC 902091 and 902092. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c2cc38534a
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