Аннотация:
The basic ionic liquid (benzyl)(dimethyl)(N,N-dimethylaminoethyl)ammonium chloride was found to be an efficient and reusable catalyst for the synthesis of spiroacenaphthylenes via the multicomponent reaction between acenaphthenequinone, malononitrile and α-methylenecarbonyl compounds (β-diketones, pyrazolones) in water.
Образец цитирования:
J. Zheng, Y. Li, “Basic Ionic Liquid-Catalyzed One-Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium”, Mendeleev Commun., 22:3 (2012), 148–149
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2771
https://www.mathnet.ru/rus/mendc/v22/i3/p148
Эта публикация цитируется в следующих 14 статьяx:
Hassan Valizadeh, Mina Ahmadi, “Direct oxidative esterification of benzaldehydes and benzylalcohols using task-specific imidazolium based perchlorate ionic liquid”, J IRAN CHEM SOC, 21:12 (2024), 2955
Goutam Brahmachari, Green Synthetic Approaches for Biologically Relevant Heterocycles, 2021, 471
Hajar Hosseini, Mohammad Bayat, “Nano SiO2 Catalyzed Chemo‐Selective Synthesis of N′‐Benzylidene‐2‐cyano‐2‐(10‐oxophenanthren‐9(10H)‐ylidene) or (2‐Oxoindolin‐3‐ylidene)acetohydrazide Derivatives”, ChemistrySelect, 6:45 (2021), 12884
Farzaneh Mohamadpour, “New role for photoexcited organic dye, Na2 eosin Y via the direct hydrogen atom transfer (HAT) process in photochemical visible-light-induced synthesis of spiroacenaphthylenes and 1H-pyrazolo[1,2-b]phthalazine-5,10-diones under air atmosphere”, Dyes and Pigments, 194 (2021), 109628
Farzaneh Mohamadpour, “Catalyst-free, visible light irradiation promoted synthesis of spiroacenaphthylenes and 1H-pyrazolo[1,2-b]phthalazine-5,10-diones in aqueous ethyl lactate”, Journal of Photochemistry and Photobiology A: Chemistry, 407 (2021), 113041
Arya Kripalaya Ratheesh, Hazel A. Sparkes, Karnam Jayarampillai Rajendra Prasad, “A new strategy for the synthesis of diverse benzo[a]carbazoles via a divergent catalytic Michael reaction”, Org. Biomol. Chem., 16:14 (2018), 2527
Mohammad Bayat, Zeinab Amiri, “Recent Developments in Acenaphthoquinone-Based Multicomponent Reactions: Synthesis of Spiroacenaphthylene Compounds”, Top Curr Chem (Z), 376:3 (2018)
Rahele Zhiani, Seyed Mohsen Sadeghzadeh, Shokufe Emrani, “Synthesis of spiroindenopyridazine-4H-pyran derivatives using Cr-based catalyst complexes supported on KCC-1 in aqueous solution”, RSC Adv., 8:12 (2018), 6259
Mohammad Bayat, Hajar Hosseini, “An efficient synthesis of novel spiroindenopyridazine-4H-pyran derivatives”, New J. Chem., 41:24 (2017), 14954
Ruby Singh, Shakeel Ahmad Ganaie, “An eco-compatible synthesis of novel spiro[acenaphthylene-1,2′[1,3]-thiazolidine]-2,4′(1H)-diones using thiamine hydrochloride as efficient catalyst in aqueous medium”, Res Chem Intermed, 43:1 (2017), 45
Ramen Jamatia, Ajay Gupta, Amarta Kumar Pal, “Nano-FGT: a green and sustainable catalyst for the synthesis of spirooxindoles in aqueous medium”, RSC Adv., 6:25 (2016), 20994
Goutam Brahmachari, Green Synthetic Approaches for Biologically Relevant Heterocycles, 2015, 185
L. O. Khafizova, R. R. Gubaidullin, N. R. Popod'ko, E. S. Meshcheryakova, L. M. Khalilov, U. M. Dzhemilev, “Zirconium-catalyzed one-pot synthesis of ɛ-spirocyclopropyl-ɛ-caprolactones”, Mendeleev Commun., 24:4 (2014), 226–228
Jia Zheng, Yiqun Li, “ChemInform Abstract: Basic Ionic Liquid‐Catalyzed One‐Pot Synthesis of the Spiroacenaphthylene Derivatives in Water Medium.”, ChemInform, 43:41 (2012)
Обратная связь: