2018
DOI: 10.1016/j.molstruc.2018.03.121
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The synthesis and investigation of different cobaloximines by spectroscopic methods

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Cited by 11 publications
(7 citation statements)
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“…In the presence of catalytic AcOH, nootkatone reacted with different hydrazides to obtain acylhydrazone derivatives N1 – N7 [34] . Then, in the presence of NaHCO 3 , nootkatone and NH 2 OH⋅HCl were refluxed at 85 °C with EtOH as the reaction solvent to obtain the oxime derivative N3 [35] . In the last, oximide derivatives N8 – N53 were prepared by the reaction of intermediate N3 with different acids and acyl chloride [36] …”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…In the presence of catalytic AcOH, nootkatone reacted with different hydrazides to obtain acylhydrazone derivatives N1 – N7 [34] . Then, in the presence of NaHCO 3 , nootkatone and NH 2 OH⋅HCl were refluxed at 85 °C with EtOH as the reaction solvent to obtain the oxime derivative N3 [35] . In the last, oximide derivatives N8 – N53 were prepared by the reaction of intermediate N3 with different acids and acyl chloride [36] …”
Section: Resultsmentioning
confidence: 99%
“…[34] Then, in the presence of NaHCO 3 , nootkatone and NH 2 OH•HCl were refluxed at 85 °C with EtOH as the reaction solvent to obtain the oxime derivative N3. [35] In the last, oximide derivatives N8-N53 were prepared by the reaction of intermediate N3 with different acids and acyl chloride. [36] Figure 3.…”
Section: Synthesis Of Target Compounds N1-n53mentioning
confidence: 99%
“…Monoxime was prepared as described in our previous study by making some modifications. [19] First, the temperature of the cryostat was adjusted to < À 5 °C, and 8.4 g of sodium metal was dissolved in ethanol (200 mL) at À 5 °C, then n-butyl nitrite (12.7 g, 0.123 mol) was added drop by drop for 30 min to the solution. After this process, (25 g, 0.123 mol) of 4'piperidinoacetophenone was taken and added gradually with a spatula within 40-50 min.…”
Section: Synthesis Synthesis Of Monoximementioning
confidence: 99%
“…In this study, monoxime and vic-dioxime ligand (LH 2 ) (1) were obtained according to the method specified in the literature. [19,20] Synthesis of the target compound (1) was achieved using 1 : 1 molar ratios (Scheme 1). The monoxime and vic-dioxime ligand (1) were characterized by NMR ( 1 H and 13 C), LC/MS/MS spectrometer, FT-IR and UV/VIS spectra, elemental analysis, and melting point.…”
Section: Synthesis and Characterizationmentioning
confidence: 99%
“…Several recent papers have presented various topics, including synthetic pathways leading to oxime complexes and structural and different coordination modes (Figure 2). The binding mode of the oxime function depends not only on the coordinative ability of the oxime group but also on the presence of atom donors in the same molecule [6][7][8][9]. For example, imidazole oximes present several donor atoms in their structures.…”
Section: Introductionmentioning
confidence: 99%