The NaY zeolite catalysed hydrolysis of nitriles to primary amides is reported. It is found that aryl nitriles with strong electron-withdrawing substituents and cyanopyridines are readily hydrolysed in the water suspension, while aliphatic nitriles do not react.
TY - JOUR
AU - Milić, Dragana
AU - Opsenica, Dejan
AU - Adnađević, Borivoj
AU - Šolaja, Bogdan
PY - 2000
UR - https://cer.ihtm.bg.ac.rs/handle/123456789/2833
AB - The NaY zeolite catalysed hydrolysis of nitriles to primary amides is reported. It is found that aryl nitriles with strong electron-withdrawing substituents and cyanopyridines are readily hydrolysed in the water suspension, while aliphatic nitriles do not react.
PB - Molecular Diversity Preservation International, Basel
T2 - Molecules
T1 - NaY zeolite: A useful catalyst for nitrile hydrolysis
VL - 5
IS - 2
SP - 118
EP - 126
DO - 10.3390/50200118
ER -
@article{
author = "Milić, Dragana and Opsenica, Dejan and Adnađević, Borivoj and Šolaja, Bogdan",
year = "2000",
abstract = "The NaY zeolite catalysed hydrolysis of nitriles to primary amides is reported. It is found that aryl nitriles with strong electron-withdrawing substituents and cyanopyridines are readily hydrolysed in the water suspension, while aliphatic nitriles do not react.",
publisher = "Molecular Diversity Preservation International, Basel",
journal = "Molecules",
title = "NaY zeolite: A useful catalyst for nitrile hydrolysis",
volume = "5",
number = "2",
pages = "118-126",
doi = "10.3390/50200118"
}
Milić, D., Opsenica, D., Adnađević, B.,& Šolaja, B.. (2000). NaY zeolite: A useful catalyst for nitrile hydrolysis. in Molecules
Molecular Diversity Preservation International, Basel., 5(2), 118-126.
https://doi.org/10.3390/50200118
Milić D, Opsenica D, Adnađević B, Šolaja B. NaY zeolite: A useful catalyst for nitrile hydrolysis. in Molecules. 2000;5(2):118-126.
doi:10.3390/50200118 .
Milić, Dragana, Opsenica, Dejan, Adnađević, Borivoj, Šolaja, Bogdan, "NaY zeolite: A useful catalyst for nitrile hydrolysis" in Molecules, 5, no. 2 (2000):118-126,
https://doi.org/10.3390/50200118 . .
