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Enantioselective Synthesis of (-)-(6R,7S)-Nitramine

  • Tehrani K
  • Boelens M
  • Yu V
  • et al.
Springer Netherlands, (2002), 407-413
DOI: 10.1007/978-94-015-9876-7_40
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Abstract

The spirocyclic (-)-(6R,7S)-nitramine was prepared in a straightforward way from an appropriately substituted chiral alpha-allylaldimine precursor involving an electrophile-induced cyclization as the key step.

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APA

Tehrani, K. A., Boelens, M., Yu, V., & De Kimpe, N. (2002). Enantioselective Synthesis of (-)-(6R,7S)-Nitramine. In Natural Products in the New Millennium: Prospects and Industrial Application (pp. 407–413). Springer Netherlands. https://doi.org/10.1007/978-94-015-9876-7_40

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