scholarly journals Post-polymerization modification of polymethacrylates enabled by keto–enol tautomerization

2020 ◽  
Vol 11 (17) ◽  
pp. 2955-2958
Author(s):  
Charles P. Easterling ◽  
Guilhem Coste ◽  
Jose E. Sanchez ◽  
Gail E. Fanucci ◽  
Brent S. Sumerlin
Keyword(s):  

We report a post-polymerization modification strategy to functionalize methacrylic copolymers through enol-ester transesterification.

Catalysts ◽  
2020 ◽  
Vol 11 (1) ◽  
pp. 21
Author(s):  
Davide Rigo ◽  
Nadia Alessandra Carmo Dos Santos ◽  
Alvise Perosa ◽  
Maurizio Selva

An unprecedented two-step sequence was designed by combining batch and continuous flow (CF) protocols for the upgrading of two aminodiol regioisomers derived from glycerol, i.e., 3-amino-1,2-propanediol and 2-amino-1,3-propanediol (serinol). Under batch conditions, at 80–90 °C, both substrates were quantitatively converted into the corresponding amides through a catalyst-free N-acetylation reaction mediated by an innocuous enol ester as isopropenyl acetate (iPAc). Thereafter, at 30–100 °C and 1–10 atm, the amide derivatives underwent a selective CF-acetalisation in the presence of acetone and a solid acid catalyst, to afford the double-functionalized (amide-acetal) products.


1983 ◽  
Vol 24 (11) ◽  
pp. 1197-1200 ◽  
Author(s):  
Diego Armesto ◽  
Maria J. Ortiz ◽  
Rafael Pérez-Ossorio ◽  
William M. Horspool

RSC Advances ◽  
2018 ◽  
Vol 8 (35) ◽  
pp. 19883-19893 ◽  
Author(s):  
Fei Ye ◽  
Peng Ma ◽  
Yue Zhai ◽  
Fei Yang ◽  
Shuang Gao ◽  
...  

Based on the structure–activity relationship and active substructure combination, a novel class of substituted 2-phenyl-2-cyclohexanedione enol ester derivatives was designed for use as potential herbicide safeners.


1975 ◽  
Vol 6 (47) ◽  
pp. no-no
Author(s):  
T. MITSUDO ◽  
Y. WATANABE ◽  
T. SASAKI ◽  
H. NAKANISHI ◽  
M. YAMASHITA ◽  
...  
Keyword(s):  

1967 ◽  
Vol 32 (12) ◽  
pp. 3934-3937 ◽  
Author(s):  
Kenneth Lee Williamson ◽  
Judith I. Coburn ◽  
Margaret F. Herr
Keyword(s):  

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