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Synlett 1995; 1995(4): 367-368
DOI: 10.1055/s-1995-4977
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An Enantioselective Synthesis of (-)-Pseudophrynaminol through Asymmetric Nitroolefination

Kaoru Fuji* , Takeo Kawabata, Toshiumi Ohmori, Manabu Node
  • *Institute for Chemical Research, Kyoto University, Uji, Kyoto 611, Japan
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Publication History

Publication Date:
31 December 2000 (online)

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Asymmetric nitroolefination of 3c afforded 2c in 97% ee, which was transformed into pseudophrynaminol (1).

pseudophrynaminol - asymmetric nitroolefination

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