Asymmetric counteranion-directed Lewis acid organocatalysis for the scalable cyanosilylation of aldehydes
Asymmetric cyanosilyation is a powerful method to convert carbonyls to chiral, configurationally stable cyanohydrins. Here, the authors report a catalyst capable of carrying out this reaction on large scales with extremely low catalyst loading, and also identify and explain a dormant period in the c...
Main Authors: | Zhipeng Zhang, Han Yong Bae, Joyram Guin, Constantinos Rabalakos, Manuel van Gemmeren, Markus Leutzsch, Martin Klussmann, Benjamin List |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2016-08-01
|
Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/ncomms12478 |
Similar Items
-
STEREO- AND REGIOSPECIFIC CATIONIC POLYMERIZATIONS VIA DESIGNED LEWIS ACIDS AND COUNTERANIONS
by: Ouchi, Makoto
Published: (2009) -
Organocatalysis
by: Benjamin List
Published: (2012-08-01) -
Organocatalysis : hydrazine and sulfonimide as new functionalities in asymmetric organocatalysis
by: He, Hao
Published: (2009) -
Asymmetric organocatalysis in flow
by: Jin, X.
Published: (2010) -
Pyrene Carboxylate Ligand Based Coordination Polymers for Microwave-Assisted Solvent-Free Cyanosilylation of Aldehydes
by: Anirban Karmakar, et al.
Published: (2021-02-01)