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Entrainer effect on photochirogenesis in near-and supercritical carbon dioxide: Dramatic enhancement of enantioselectivity

  • Yasuhiro Nishiyama
  • , Takehiko Wada
  • , Sadayuki Asaoka
  • , Tadashi Mori
  • , Taylor A. McCarty
  • , Nadine D. Kraut
  • , Frank V. Bright
  • , Yoshihisa Inoue
  • The University of Osaka
  • SUNY Buffalo

Research output: Contribution to journalArticlepeer-review

22 Scopus citations

Abstract

Diethyl ether added as an entrainer (cosolvent) to near- and supercritical CO2 significantly enhanced the enantioselectivity of photocyclization of 5,5-diphenyl-4-penten-1-ol sensitized by saccharide naphthalenedicarboxylate to give a cyclization product in enantiomeric excesses much larger than those obtained in conventional organic solvents, revealing the unique features of nc- and sc-CO2 as well as the critical role of entrainer clustering to the intervening diastereomeric exciplex pair.

Original languageEnglish
Pages (from-to)7526-7527
Number of pages2
JournalJournal of the American Chemical Society
Volume130
Issue number24
DOIs
StatePublished - Jun 18 2008

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