Oxone-sodium nitrite mediatedN-nitrosamines formation under mild conditions from secondary amines

2019 ◽  
Vol 49 (17) ◽  
pp. 2270-2279 ◽  
Author(s):  
Pinki Gaur ◽  
Shaibal Banerjee
2012 ◽  
Vol 550-553 ◽  
pp. 1590-1594 ◽  
Author(s):  
Hua Yang ◽  
Pei Pei Meng ◽  
Rui Wang ◽  
Pei Ran Li ◽  
Peng Li ◽  
...  

N-nitrosamine is a kind of carcinogenic substance, which is possibly formed in the reaction of nitrites with amino acids or secondary amines. Two in vitro model systems were designed to evaluate the influence of oxidized myofibrils protein subjected to repeated freeze-thaw cycles (0, 1, 2, 3, 4, 7, 10 times) on N-nitrosamine formation. Model system I contains diethylamine and sodium nitrite, while model system II contains only sodium nitrite as reaction solution. Oxidized myofibrils protein were added to both systems. The results revealed that as the number of freeze-thaw cycles increased, cross-linking of myosin heavy chains and the content of protein carbonyl increased, but the content of protein sulfydryl decreased, which indicates oxidization of protein occurred. The concentration of N-nitrosodiethylamine increased as the number of freeze-thaw cycles increased, especially after four cycles. Oxidized myofibrils protein promoted the formation of N-nitrosodiethylamine. The more the times of freeze-thaw cycles were subjected, the more oxidization of myofibrils protein occurred and the higher yield of the N-nitrosodiethylamine.


2007 ◽  
Vol 11 (07) ◽  
pp. 537-546 ◽  
Author(s):  
Clifford C. Leznoff ◽  
Annette Hiebert ◽  
Sibel Ok

Primary amines, secondary amines and tertiary butyl esters of amino acids are used as nucleophiles with zinc(II) hexadecafluorophthalocyanine to provide mixtures of mono and disubstituted fluorinated phthalocyanines under mild conditions, or polyaminosubstituted phthalocyanines when using the amines as solvents. Diamines give cyclic substituted phthalocyanines, binuclear or trinuclear phthalocyanines or mixtures of both types, depending on the chain length or structure of the diamine.


RSC Advances ◽  
2016 ◽  
Vol 6 (92) ◽  
pp. 89979-89983 ◽  
Author(s):  
Xiaolei Zhu ◽  
Li Qiao ◽  
Pingping Ye ◽  
Beibei Ying ◽  
Jun Xu ◽  
...  

We report the first example of copper(ii) catalyzed remote C–H nitration of 8-aminoquinoline amides by using sodium nitrite as nitration reagent under mild conditions in 1 minute which undergoes single electron process.


2020 ◽  
Vol 22 (6) ◽  
pp. 1832-1836
Author(s):  
Shi Jiang ◽  
Eric Muller ◽  
François Jerôme ◽  
Marc Pera-Titus ◽  
Karine De Oliveira Vigier

Catalytic conversion of furfural to secondary tetrafurfurylamine under mild conditions of temperature and hydrogen pressure.


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