Faculty Opinions recommendation of Development of highly diastereo- and enantioselective direct asymmetric aldol reaction of a glycinate Schiff base with aldehydes catalyzed by chiral quaternary ammonium salts.

Author(s):  
Carlos F Barbas
RSC Advances ◽  
2016 ◽  
Vol 6 (79) ◽  
pp. 75470-75477 ◽  
Author(s):  
Haifeng Wang ◽  
Linjie Yan ◽  
Fangjun Xiong ◽  
Yan Wu ◽  
Fener Chen

Several novel chiral Schiff base ligands were prepared from a commercially available chloramphenicol base and applied to the titanium-mediated asymmetric aldol reaction of diketene with various α,β-unsaturated aldehydes.


2011 ◽  
Vol 239-242 ◽  
pp. 496-500
Author(s):  
Li Ju Tan ◽  
He Dong Wang ◽  
Jiang Tao Wang

Schiff base of chitosan was obtained by the reaction of chitosan and aromatic aldehyde, and then Schiff base of chitosan reacted with methyl iodide to get soluble quaternary ammonium salts of chitosan which were N-metoxybenzenemethyl quaternary ammonium salt of chitosan (NM- Chitosan) and N-hydroxybenzenemethyl quaternary ammonium salt of chitosan(NH-Chitosan). The obtained chitosan derivatives were characterized by Infrared Spectra Analysis(FT-IR), Nuclear Magnetic Resonance Spectroscopy(1H NMR) and elemental analysis. Quantitative analysis showed that there was small difference between degrees of quaternization(DQ) and degrees of substitution(DS), and the solubility of chitosan derivatives was demonstrated to be better in the organic solvents.


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