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1
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64349085069
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(ca. 20%) were observed. On the basis of the kinetic parameters, steric kinetic isotope effect, and 1H NMR spectra of the nondeuteriated and deuteriated rotaxanes, we propose a deslipping mechanism involving pre-equilibrium. © 2009 American Chemical Society.
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(ca. 20%) were observed. On the basis of the kinetic parameters, steric kinetic isotope effect, and 1H NMR spectra of the nondeuteriated and deuteriated rotaxanes, we propose a deslipping mechanism involving pre-equilibrium. © 2009 American Chemical Society.
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2
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64349096970
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3, which was prepared according to the reported procedure: Sawada, M.; Hagita, K.; Imamura, H.; Tabuchi, H.; Yododa, S.; Umeda, M.; Takai, Y.; Yamada, H.; Yamaoka, H.; Hirose, K.; Tobe, Y.; Tanaka, T.; Takahashi, S. J. Mass Spectrom. Soc. Jpn 2000, 48, 323-332. The degree of isotopic labeling (<98%) was determinined by 1H NMR and mass spectra, and the enantiomeric excess (<99%) was checked by HPLC using a chiral column.
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3, which was prepared according to the reported procedure: Sawada, M.; Hagita, K.; Imamura, H.; Tabuchi, H.; Yododa, S.; Umeda, M.; Takai, Y.; Yamada, H.; Yamaoka, H.; Hirose, K.; Tobe, Y.; Tanaka, T.; Takahashi, S. J. Mass Spectrom. Soc. Jpn 2000, 48, 323-332. The degree of isotopic labeling (<98%) was determinined by 1H NMR and mass spectra, and the enantiomeric excess (<99%) was checked by HPLC using a chiral column.
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