Back to Search Start Over

Racemization and Deracemization through Intermolecular Redox Behaviour.

Authors :
Engwerda, Anthonius H. J.
Meekes, Hugo
Bickelhaupt, F. Matthias
Rutjes, Floris P. J. T.
Vlieg, Elias
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