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2000
Volume 19, Issue 8
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

The isosteviol derived bifunctional primary amine-squaramide organocatalysts were applied in the Michael addition between nitroalkenes and acetophenone. The conjugate addition isomers of two configurations were observed with high yields (up to 93% yield) and good enantioselectivity (up to 91% ee) at room temperature.

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/content/journals/loc/10.2174/1570178619666220112124054
2022-08-01
2025-09-09
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/content/journals/loc/10.2174/1570178619666220112124054
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  • Article Type:
    Research Article
Keyword(s): asymmetric catalysis; Isosteviol; michael reaction; nitroalkenes; organocatalyst; squaramide
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