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Compared to the ee, the er better and, importantly, more intuitively, reflects enantioselectivity. er Values of 3:1, 19:1, and 199:1 correspond, respectively, to ee values of 50.0, 90.0, and 99.0%. For an interesting discussion, see
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Compared to the ee, the er better and, importantly, more intuitively, reflects enantioselectivity. er Values of 3:1, 19:1, and 199:1 correspond, respectively, to ee values of 50.0, 90.0, and 99.0%. For an interesting discussion, see: B. C. Gibb, Nat. Chem. 2012, 4, 237-238.
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The presence of excess nitrosobenzene (2), the α-aminoxylation products usually undergo O-N bond cleavage to afford the corresponding α-hydroxylated products. None of the α-aminoxylation and α-hydroxylated products were detected.
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In the presence of excess nitrosobenzene (2), the α-aminoxylation products usually undergo O-N bond cleavage to afford the corresponding α-hydroxylated products. None of the α-aminoxylation and α-hydroxylated products were detected.
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CCDC904904, CCDC904905, and CCDC904903 contain the supplementary crystallographic data for compounds 3e, 3c, and 5b. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via. The absolute configuration of 3e could be determined unambiguously from its structural data [Flack parameter: -0.007(9)], and the absolute configurations of compounds 3a-m and 5b were assigned by analogy with 3e.
-
CCDC904904, CCDC904905, and CCDC904903 contain the supplementary crystallographic data for compounds 3e, 3c, and 5b. These data can be obtained free of charge from the Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif. The absolute configuration of 3e could be determined unambiguously from its structural data [Flack parameter: -0.007(9)], and the absolute configurations of compounds 3a-m and 5b were assigned by analogy with 3e.
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84877068831
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The proposed approach in the transition state is fully consistent with earlier proposals for related organocatalysts and reactions, some of which were examined theoretically:
-
The proposed approach in the transition state is fully consistent with earlier proposals for related organocatalysts and reactions, some of which were examined theoretically:.
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We define eco-compatible as both ecologically and economically compatible.
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