Cyclopropane ring formation through enantioselective deprotonation of Cs-symmetric cyclohept-4-enone oxides

Hitoshi Abe, Takenori Tsujino, Daisuke Tsuchida, Setsuo Kashino, Yasuo Takeuchi, Takashi Harayama

Research output: Contribution to journalArticle

10 Citations (Scopus)

Abstract

Using a chiral lithium amide base, the asymmetric deprotonation reaction of Cs-symmetric cyciohept-4-enone oxides was examined to form an optically active cyclopropane compound.

Original languageEnglish
Pages (from-to)503-508
Number of pages6
JournalHeterocycles
Volume56
Issue number1-2
Publication statusPublished - Jan 1 2002

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ASJC Scopus subject areas

  • Analytical Chemistry
  • Pharmacology
  • Organic Chemistry

Cite this

Abe, H., Tsujino, T., Tsuchida, D., Kashino, S., Takeuchi, Y., & Harayama, T. (2002). Cyclopropane ring formation through enantioselective deprotonation of Cs-symmetric cyclohept-4-enone oxides. Heterocycles, 56(1-2), 503-508.