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- W2109175462 endingPage "758" @default.
- W2109175462 startingPage "737" @default.
- W2109175462 abstract "Recent progress in asymmetric catalysis has contributed to the development of a diverse range of chiral organocatalysts that differ in their origin, structure and mode of activation. The bifunctional organocatalysts bearing aromatic hydroxyl (or phenolic) groups have emerged as a privileged class of organocatalyst. In these bifunctional organocatalysts, the aromatic hydroxyl group functions as a weak Brønsted acid or hydrogen bonding site and a nucleophilic or basic moiety such as amine and phosphine serve as a base or hydrogen bond acceptor. The bifunctional organocatalysts having these moieties have not been reviewed. In this review we are presenting the asymmetric transformations catalyzed by the bifunctional organocatalyst bearing an aromatic hydroxyl group." @default.
- W2109175462 created "2016-06-24" @default.
- W2109175462 creator A5016285909 @default.
- W2109175462 creator A5045216986 @default.
- W2109175462 date "2012-01-01" @default.
- W2109175462 modified "2023-10-01" @default.
- W2109175462 title "Aromatic hydroxyl group—a hydrogen bonding activator in bifunctional asymmetric organocatalysis" @default.
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