2015
DOI: 10.1016/j.molliq.2015.01.013
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Effective preparation of hexahydroquinolines under ambient and solvent-free conditions

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Cited by 13 publications
(8 citation statements)
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“…Afterwards, the 2-benzylidenedimedone (1) and enamine (2) 60 90 19 2 3 60 49 79 3 5 60 26 84 4 7 60 15 (continued on next page) to the activated carbonyl group. The mechanism is confirmed by the literatures [17,32,33].…”
Section: Catalyst Activitysupporting
confidence: 85%
“…Afterwards, the 2-benzylidenedimedone (1) and enamine (2) 60 90 19 2 3 60 49 79 3 5 60 26 84 4 7 60 15 (continued on next page) to the activated carbonyl group. The mechanism is confirmed by the literatures [17,32,33].…”
Section: Catalyst Activitysupporting
confidence: 85%
“…All of the desired product(s) were characterized by comparison of their physical and spectral data (melting points, IR, 1 H NMR) with those of known compounds. 15,27,28 2.1.9. Effect of impurity of water on the catalytic activity of 2-ethyl imidazolium hydrogen sulfate.…”
Section: Resultsmentioning
confidence: 99%
“…All of the desired product(s) were characterized by comparison of their physical and spectral data (melting points, IR, 1 H NMR) with those of known compounds. 15,[27][28] …”
Section: Catalyst Recyclingmentioning
confidence: 99%
“…In continuation of our previously reported methodologies for designing, synthesis and applications of task specific ionic liquids (TSILs) [32][33][34][35][36][37][38][39][40], herein, the synthesis of novel neutral media ionic liquid 2-ethyl imidazoliumacetate OAc from available and inexpensive starting materials (Scheme 1), and its full characterization by using FT-IR, 1 H NMR, 13 C NMR, UV, TG (thermal gravimetric), DTG (derivative thermal gravimetric), and pH controlling in aqueous media is reported. Afterward, the abovementioned ionic liquid was used as a highly efficient, homogeneous and recyclable catalyst for the preparation of 2-amino-4H-chromene derivatives via the one-pot multi-component condensation of various aldehydes, malononitrile, and resorcinol under thermal solvent-free conditions (Scheme 2).…”
Section: Introductionmentioning
confidence: 86%