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- W2950653218 abstract "An organophosphane catalyst derived from L-proline was shown to be a very effective catalyst for asymmetric Michael addition reactions of various chalcones to cyclic ketones including both cyclohexanone and cyclopentanone. The corresponding adducts could be obtained in high yields (up to 91 %) and with excellent enantioselectivities (up to 99 % ee) and diastereomeric ratios (up to >99:1). A possible catalytic mechanism, based on 31P NMR and ESI-MS observations, for this organophosphane-catalyzed Michael addition has been proposed." @default.
- W2950653218 created "2019-06-27" @default.
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- W2950653218 date "2013-08-30" @default.
- W2950653218 modified "2023-09-27" @default.
- W2950653218 title "ChemInform Abstract: Asymmetric Michael Addition of Cyclohexanone or Cyclopentanone to Chalcones Catalyzed by an L-Proline-Based Organic Phosphane." @default.
- W2950653218 cites W2130683558 @default.
- W2950653218 doi "https://doi.org/10.1002/chin.201338082" @default.
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