MONOXLORSIRKA KISLOTANING ETIL EFIRI VA AMIDINING UCHLAMCHI AMINLAR BILAN REAKSIYASINI O‘RGANISH
##submission.downloads##
Monoxlorsirka kislotaning R-C2 H5 , -C4 H9 va monoxlorsirka kislotaning amidi sintez qilindi. Olingan monoxlorsirka kislotaning efirlari va amidini xromotografik usullarda tozalandi. Uchlamchi aminlar sifatida trimetilamin, trietilaminlar bilan reaksiyalar olib borildi. Reaksiya mexanizmi nukleofil birikish mexnizmida boradi va to’rtlamchi ammoniy tuzlari sintez qilindi. Olib borilgan reaksiyalarning muqobil sharoitlari o’rganildi. Sintez qilingan to’rtlamchi ammoniy tuzlarini biologik faollilklari o’rganildi va o’simliklarni o’sishini boshqaruvchi stimulyatorlik xossalari mavjud ekanligi aniqlandi. Olingan to’rtlamchi ammoniy tuzlarini fizik-kimyoviy tahlillar (IQ, PMR) spektrlari olindi va tahlill qilindi
Xoliqov TURSINALI. (2025). MONOXLORSIRKA KISLOTANING ETIL EFIRI VA AMIDINING UCHLAMCHI AMINLAR BILAN REAKSIYASINI O‘RGANISH. «O‘zMU XABARLARI», 3(3.2.1), 342–344. https://doi.org/10.69617/nuuz.v3i3.2.1.5746
F. Bureš, Top. Curr. Chem., 2019, 377, 14; (b) C. W. Weston, J. R. Papcun and M. Dery, Ammonium compounds, in Kirk–Othmer encyclopedia of chemical technology, Wiley, NY, 2003, vol. 2, pp. 711–762.
2. S. Mehan, V. K. Aswal and J. Kohlbrecher, Langmuir, 2014, 30, 9941–9950; (b) S. Mishra and V. K. Tyagi, J. Oleo Sci., 2007, 56, 269–276.
3. M. Watanabe, M. L. Thomas, S. Zhang, U. Kazuhide, Y. Tomohiro and D. Kaoru, Chem. Rev., 2017, 117, 7190–7239; (b) V. Selvamani, V. Suryanarayanan, D. Velayutham and S. Gopukumar, J. Solid State Electrochem., 2016, 20, 2283–2293.
4. J.Přech, P. Pizarro, D. P. Serrano and J. Čejka, Chem. Soc. Rev., 2018, 47, 8263–8830; (b) R. Bai, Q. Sun, N. Wang, Y. Zou, G. Guo, S. Iborra, A. Corma and J. Yu, Chem. Mater., 2016, 28, 6455–6458.
5. For recent reviews see: (a) T. Nakamura, K. Okuno, R. Nishiyori and S. Shirakawa, Chem. – Asian J., 2020, 15, 463–472; (b) D. Kristofikova, V. Modrock, M. Meciarova and R. Sebesta, ChemSusChem, 2020, 13, 2828–2858; (c) L. Roiser, K. Zielke and M. Waser, Asian J. Org. Chem., 2018, 7, 852–864; (d) D. Qian and J. Sun, Chem. – Eur. J., 2018, 25, 3740–3751; (e) K. C. Lethesh, W. Dehaen and K. Binnemans, RSC Adv., 2014, 4, 4472–4477.
6. M. Pateiro-Moure, M. Arias-Estevez and J. Simal- Gandara, Environ. Sci. Technol., 2013, 47, 4984–4998; (b) T. Nardin, C. Barnaba, F. Abballe, G. Trenti, M. Malacarne and R. Larcher, J. Sep. Sci., 2017, 40, 3928–3937.
7. For selected articles see: (a) P. I. Hora, S. G. Pati, P. J. McNamara and W. A. Arnold, Environ. Sci. Technol. Lett., 2020, 7, 622–631; (b) P. Makvandi, R. Jamaledin, M. Jabbari, N. Nikfarjam and A. Borzacchiello, Dent. Mater., 2018, 34, 851–867; (c) M. C. Jennings, K. P. C. Minbiole and W. M. Wuest, ACS Infect. Dis., 2015, 1, 288–303; d) J. Pernak, Przemysł Chem., 2013, 92, 1653–1656.
8. Jee Sun Yang, Doona Song, Boah Lee, Won Jin Ko, Song-Kyu Park, Misun Won, Kiho Lee, Hwan Mook Kim, Gyoonhee Hana. Synthesis and biological evaluation of novel aliphatic amido-quaternary ammonium salts for anticancer chemotherapy: Part I. European Journal of Medicinal Chemistry 46 (2011) 2861-2866
2. S. Mehan, V. K. Aswal and J. Kohlbrecher, Langmuir, 2014, 30, 9941–9950; (b) S. Mishra and V. K. Tyagi, J. Oleo Sci., 2007, 56, 269–276.
3. M. Watanabe, M. L. Thomas, S. Zhang, U. Kazuhide, Y. Tomohiro and D. Kaoru, Chem. Rev., 2017, 117, 7190–7239; (b) V. Selvamani, V. Suryanarayanan, D. Velayutham and S. Gopukumar, J. Solid State Electrochem., 2016, 20, 2283–2293.
4. J.Přech, P. Pizarro, D. P. Serrano and J. Čejka, Chem. Soc. Rev., 2018, 47, 8263–8830; (b) R. Bai, Q. Sun, N. Wang, Y. Zou, G. Guo, S. Iborra, A. Corma and J. Yu, Chem. Mater., 2016, 28, 6455–6458.
5. For recent reviews see: (a) T. Nakamura, K. Okuno, R. Nishiyori and S. Shirakawa, Chem. – Asian J., 2020, 15, 463–472; (b) D. Kristofikova, V. Modrock, M. Meciarova and R. Sebesta, ChemSusChem, 2020, 13, 2828–2858; (c) L. Roiser, K. Zielke and M. Waser, Asian J. Org. Chem., 2018, 7, 852–864; (d) D. Qian and J. Sun, Chem. – Eur. J., 2018, 25, 3740–3751; (e) K. C. Lethesh, W. Dehaen and K. Binnemans, RSC Adv., 2014, 4, 4472–4477.
6. M. Pateiro-Moure, M. Arias-Estevez and J. Simal- Gandara, Environ. Sci. Technol., 2013, 47, 4984–4998; (b) T. Nardin, C. Barnaba, F. Abballe, G. Trenti, M. Malacarne and R. Larcher, J. Sep. Sci., 2017, 40, 3928–3937.
7. For selected articles see: (a) P. I. Hora, S. G. Pati, P. J. McNamara and W. A. Arnold, Environ. Sci. Technol. Lett., 2020, 7, 622–631; (b) P. Makvandi, R. Jamaledin, M. Jabbari, N. Nikfarjam and A. Borzacchiello, Dent. Mater., 2018, 34, 851–867; (c) M. C. Jennings, K. P. C. Minbiole and W. M. Wuest, ACS Infect. Dis., 2015, 1, 288–303; d) J. Pernak, Przemysł Chem., 2013, 92, 1653–1656.
8. Jee Sun Yang, Doona Song, Boah Lee, Won Jin Ko, Song-Kyu Park, Misun Won, Kiho Lee, Hwan Mook Kim, Gyoonhee Hana. Synthesis and biological evaluation of novel aliphatic amido-quaternary ammonium salts for anticancer chemotherapy: Part I. European Journal of Medicinal Chemistry 46 (2011) 2861-2866
.jpg)
.png)
