Asymmetric Access to the Smallest Enolate Intermediate via Organocatalytic Activation of Acetic Ester

2013 ◽  
Vol 15 (22) ◽  
pp. 5822-5825 ◽  
Author(s):  
Shaojin Chen ◽  
Lin Hao ◽  
Yuexia Zhang ◽  
Bhoopendra Tiwari ◽  
Yonggui Robin Chi
Keyword(s):  
1990 ◽  
Vol 31 (35) ◽  
pp. 5089-5092 ◽  
Author(s):  
Mercades Alvarez ◽  
Marisa Salas ◽  
Anna de Veciana ◽  
Rodolfo Lavilla ◽  
Joan Bosch

2018 ◽  
Vol 2018 ◽  
pp. 1-8
Author(s):  
Fangfang Cheng ◽  
Bingbing Wang ◽  
Yanzhi Xia

A novel amphipathic chitosan derivative, O-acetyl-chitosan acetic ester (ACHA), was synthesized by the reaction of chitosan with acetic acid in the presence of thionyl chloride. The physicochemical properties of ACHA were characterized by FTIR, 1H NMR, TGA, and XRD. The yield (Y) of ACHA was 79.4%, and the degree of acetylation (DA) of ACHA was 1.04. Compared to CS, ACHA could be dissolved in many organic solvents, deionized water, and aqueous solution. Our results showed that ACHA exhibited a superior antibacterial activity against Escherichia coli, Pseudomonas aeruginosa, and Staphylococcus aureus. These findings indicated that ACHA was preferable for use as antimicrobial agents in wound healing, food preservative, and tissue engineering.


1938 ◽  
Vol 34 ◽  
pp. 351 ◽  
Author(s):  
Ph. Gross ◽  
H. Steiner ◽  
F. Krauss
Keyword(s):  

1908 ◽  
Vol 93 (0) ◽  
pp. 1070-1074 ◽  
Author(s):  
Martin Onslow Forster ◽  
Hans Eduard Fierz ◽  
Walter Philip Joshua

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