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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Sprache: | eng |
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Zusammenfassung: | 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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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c2cc38534a |