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31
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Ref. 8b.
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Ref. 8b.
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34
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43
-
-
39249084256
-
-
note
-
To maximize the enantioselectivity of the product, the reaction was stopped upon 50-70% conversion.
-
-
-
-
44
-
-
39249083679
-
-
note
-
(E)-Cinnamaldehyde, (E)-cinnamic acid, (E)-ethyl cinnamate, and (E)-cinnamamide are all inert to our oxidation conditions.
-
-
-
-
45
-
-
39249084933
-
-
note
-
(E)-4,4-Dimethyl-1-phenylpent-1-en-3-one and (E)-4,4-dimethyl-1-phenylpent-2-en-1-one are inert to our oxidation conditions. For other unsuccessful α,β-unsaturated ketones we screened, see: Supplementary data.
-
-
-
-
46
-
-
39249084523
-
-
note
-
After work-up, brucine and BNO are isolated in >95% yield as a 9:1 mixture.
-
-
-
-
47
-
-
34447102708
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For a review on highly concentrated reactions, see:
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Walsh, P.J.1
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