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note
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Complementary strands of ODN6 containing natural bases (A, T, and G) were also examined to investigate the counter base effect. The DNA metalloenzymes by the combination of triethylene glycol and a counter base A, T, or G afforded lower enantioselectivities of product compared with a counter base C (entries 1-3 in Table S2).
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36
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84938732842
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note
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In the case of dienophile including a p-nitro group on the phenyl ring, a decrease in enantioselectivity was observed using a Cu(II)-DNA-triethylene glycol conjugate (99% conversion, endo/exo = 18/1, -59% ee).
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The control experiment using a Cu(II)-dmbpy/ODN6/ODN15 system afforded the Diels-Alder product with -87% ee, endo/exo ratio of 36:1 and 97% conversion.
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