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Racemization and Deracemization through Intermolecular Redox Behaviour.
- Source :
- Chemistry - A European Journal; 7/22/2019, Vol. 25 Issue 41, p9639-9642, 4p
- Publication Year :
- 2019
-
Abstract
- Chiral molecules exhibiting a quinone and/or hydroquinone moiety are ubiquitous in natural products and small molecule drugs. Herein, we describe a chiral quinone‐hydroquinone molecule that racemizes through a reversible redox reaction. Using a combined computational and experimental approach, we show that this racemization proceeds via an intermolecular reaction mechanism. Starting from two achiral reactants, this molecule could be obtained in enantiopure form using Viedma ripening. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 09476539
- Volume :
- 25
- Issue :
- 41
- Database :
- Complementary Index
- Journal :
- Chemistry - A European Journal
- Publication Type :
- Academic Journal
- Accession number :
- 137774460
- Full Text :
- https://doi.org/10.1002/chem.201902438