Published in

American Association for the Advancement of Science, Science, 6463(366), p. 364-369, 2019

DOI: 10.1126/science.aay2204

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Light-driven deracemization enabled by excited-state electron transfer

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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Abstract

Charging through the looking glass Asymmetric catalysis is a commonly applied technique to prepare just one of two mirror-image products in a chemical reaction. But what if you already have the compound you want, stuck in a mixture of left- and right-handed enantiomers? Shin et al. now show that light-induced electron transfer can trigger a favorable succession of proton and hydrogen-atom transfer steps, both of which are susceptible to biasing by catalysts, to preferentially convert a mixture of cyclic urea enantiomers into just one (see the Perspective by Wendlandt). Science , this issue p. 364 ; see also p. 304