2014
DOI: 10.1007/s10600-014-1067-9
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Electrochemical Synthesis of Amino Derivatives of Biflavonoids

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Cited by 7 publications
(9 citation statements)
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“…Once the electrolysis was completed, about 90% of the acetonitrile was distilled from the anode compartment. Further purification using chromatography column was applied and followed by recrystallization to obtain the biflavonoid product with a good yield (60–70%) [82] .…”
Section: Synthetic Sourcesmentioning
confidence: 99%
“…Once the electrolysis was completed, about 90% of the acetonitrile was distilled from the anode compartment. Further purification using chromatography column was applied and followed by recrystallization to obtain the biflavonoid product with a good yield (60–70%) [82] .…”
Section: Synthetic Sourcesmentioning
confidence: 99%
“…The lack of high speeds inside the screw pumps makes them promising for use as dredging pumps that drain rainwater into the collection network [11][12][13][14]. However, these pumps have not been widely used in the sewer industry [15][16][17][18][19]. This is due to the fact that traditional designs of screw pumps have a number of disadvantages that hinder their widespread adoption [20].…”
mentioning
confidence: 99%
“…The installation will make possible to change the angle of inclination of the screw a, its rotation frequency n, water level in the channel in front of the screw, as well as the gap between the screw and the tray in which it rotates . It is known that the total pump efficiency η povn consists of its mechanical η mex , hydraulic η gidr and volumetric efficiency η obemn and is determined by the equation ( 16) (16) Mechanical efficiency depends on the design of the pump. In the experimental setup, an electric drive with a single-stage reduction unit is used.…”
mentioning
confidence: 99%
“…However, known methods for synthesizing flavopiridol analogs [2, 3] are complicated and multi-step. Therefore, the successful electrochemical synthesis of biflavonoids and their N-containing analogs [4,5] allowed us to propose that it can be used to synthesize new flavopiridol analogs.Chrysine (0.254 g, 1 mmol, Aldrich) was dissolved in MeCN (250 mL), treated with LiClO 4 (0.110 g) and morpholine (0.520 mL), and electrolyzed in a diaphragm cell at a Pt anode with a working surface of 2 cm 2 and current 12 mA. KCl (0.5 g) was mixed with the anode liquor after 3 h of electrolysis, which then was continued for 2.5 h. When the electrolysis was finished, about 90% of the solvent was distilled from the anode liquor.…”
mentioning
confidence: 99%
“…However, known methods for synthesizing flavopiridol analogs [2,3] are complicated and multi-step. Therefore, the successful electrochemical synthesis of biflavonoids and their N-containing analogs [4,5] allowed us to propose that it can be used to synthesize new flavopiridol analogs.…”
mentioning
confidence: 99%