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Anion-Mediated, Stereospecific Synthesis of Secondary and Tertiary Cyclopropylboronates from Chiral Epoxides and gem-Diborylalkanes

  • Gwanggyun Kim
  • , Minjae Kim
  • , Changsu Ryu
  • , Juhyeok Choi
  • , Seung Hwan Cho*
  • *Corresponding author for this work
  • Pohang University of Science and Technology
  • Yonsei University

Research output: Contribution to journalJournal articlepeer-review

Abstract

We report a transition-metal-free deborylative cyclization approach to synthesize enantioenriched secondary and tertiary cyclopropylboronates using γ-phosphate-containing gem-diborylalkanes derived from chiral epoxides and gem-diborylalkanes. Our method enables the synthesis of a broad range of enantioenriched secondary and tertiary cyclopropylboronates in good yields with excellent stereospecificity. We demonstrate the versatility of our approach by performing a gram-scale reaction. We also show that the enantioenriched tertiary cyclopropylboronates can be transformed into a wide array of enantioenriched cyclopropane derivatives in a stereospecific boron-group transformation.

Original languageEnglish
Pages (from-to)4130-4134
Number of pages5
JournalOrganic Letters
Volume25
Issue number22
DOIs
StatePublished - 2023.06.9

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