Synthesis of Amidophosphates Based on 1-Ethynyl-1-Aminocyclohexane Upon Microwave Activation and their Biological Activity

(1). B.Zh. Dzhiembaev, α-oxy- and α-aminophos¬phonates hexagonal (Ν, O, S, Se) heterocycles, Almaty, Kompleks, 2003, 234 p. [in Russian].

(2). E.E. Nifant’ev, Soros Educational Journal 7 (1996) 39‒46 [in Russian]. URL

(3). J. Romanowska, K. Kolodziej, M. Sobkowski, M. Rachwalak, et a., Eur. J. Med. Chem. 164 (2019) 47‒58. Crossref

(4). R. Bahadi, M. Berredjem, R. Redjemia, S. Bouacida, et al., Phosphorus, Sulfur, Silicon Relat. Elem. 197 (2022) 1248‒1254. Crossref

(5). A.V. Smolobochkin, A.S. Gazizov, K.A. Doszhanova, A.B. Kuandykova, et al., Russ. J. Gen. Chem. 90 (2020) 1100–1103. Crossref

(6). I. Romero-Estudillo, J.L. Viveros-Ceballos, O. Cazares-Carreño, A. González-Morales, et al., Bioorg. Med. Chem. 27 (2019) 2376‒2386. Crossref

(7). Patent KZ 35444. Application of N-(1- ethylcyclohexyl)amide O,O-diethyl phosphoric acid as a growth stimulator of vegetable crops. B.Zh. Dzhiembaev, A.B. Kuandykova, K.A. Doszhanova, A.A. Tleubaeva et al. Bull. #52, 2021.

(8). I.H. Kim, Y.K. Park, H. Nishiwaki, B.D. Hammock, et al., Med. Chem. 23 (2015) 7199‒7210. Crossref

(9). F.M. Harassova, D.Sh. Safina, N-Amine Phosphorylation by Todd-Atterton. Review (N-Fosforilirovanie aminov po Toddu- Attertonu. Obzor. F.M. Harrasova, D.Sh. Safina, Dep. rukopisi. № 250. – HP 92 ot 5.08.92. RZhHim. 1993. 8 Zh 357 Dep.) [in Russian].

(10). R. Bahadi, R. Boughoula, M. Berredjem, K. Bachari, et al., Phosphorus, Sulfur, Silicon Relat. Elem. 197 (2022) 1150‒1156. Crossref

(11). R. Aissa, S. Guezane-Lakoud, L. Gali, M. Toffano, et al., J. Mol. Struct. 1247 (2022) 131336. Crossref

(12). L.A. Kosykhova, Yu.V.K. Pikshilingaite, A.S. Zaks, Yu.M. Rabotnikov, Pharm. Chem. J. 30 (1996) 330‒331. Crossref

(13). V.A. Glushkov, O.S. P’yankova, L.V. Anikina, Yu.B. Vikharev, et al., Pharm. Chem. J. 40 (2006) 298‒302. Crossref

(14). H.R. Hudson, Á. Tajti, E. Bálint, M. Czugler, et al., Synth. Commun. 50 (2020) 1446‒1455. Crossref

(15). S. Poola, S. Nagaripati, S. Tellamekala, V. Chintha, et al., Synth. Commun 50 (2020) 2655‒2672. Crossref

(16). S.K. Tukanova, B.Zh. Dzhiembaev, B.M. Butin, Fosforilirovanie 1-jetinil-1-aminociklogeksana dialkilfosforistymi kislotami, Zh. obshh. himii. 59 (1989) 2633–2634 (in Russian).

(17). Patent KZ 35532. Application of 0,0-dieth¬yl-1-(3,4-dimethoxyphenyl)-(1-ethynylcyclo-hexylaminomethyl) phosphonate as a growth stimulator of vegetable crops. B.Zh. Dzhiem-baev, A.B. Kuandykova, K.A. Doszhanova, A.A. Tleubaeva et al. Bull. #8, 2022.

(18). A.B. Kuandykova, B.Zh. Dzhiembaev, K.A. Doszhanova, Bulletin of the National Engineering Academy of the Republic of Kazakhstan 4 (2019) 66‒72 [in Russian].

(19). L.I. Minaeva, L.S. Patrikeeva, M.M. Kabachnik, I.P. Beletskaya, Russ. J. Org. Chem. 46 (2010) 1579–1580. Crossref

(20). V.I. Krutikov, A.V. Erkin, V.V. Krutikova, Russ. J. Gen. Chem. 82 (2012) 822–826. Crossref

(21). Z. Rádai, N.Z. Kiss, Z. Mucsi, G. Keglevich, Phosphorus, Sulfur, Silicon Relat. Elem. 191 (2016) 1564‒1565. Crossref

(22). A. Adhikari, S. Bhakta, T. Ghosh, Tetrahedron 126 (2022) 133085. Crossref

(23). G.M. Sheldrick, T.R. Schneider, Methods Enzymol. 277 (1997) 319–343. PMID: 18488315

(24). A. Altomare, G. Cascarano, C. Giacovazzo, D. Viterbo, Acta Cryst. 47 (1991) 744‒748. Crossref

(25). G.M. Sheldrick, (1997) SHELXS97 and SHELXL97. Program for Crystal Structure Solution and Refinement. University of Göttingen, Göttingen. URL

(26). L.J. Farrugia J. Appl. Crystallogr. 32 (1999) 837‒838. Crossref

(27). APEX2 (Version 2.1) (2006). SAINTPlus. Data Reduction and Correction Program (Version 7.31A), Bruker Advanced X-ray Solutions, Bruker AXS Inc., Madison. Wisconsin. USA URL

(28). A.L. Spek, Acta Cryst. 65 (2009) 148‒155. Crossref

留言 (0)

沒有登入
gif