2017
DOI: 10.1016/j.chroma.2017.07.051
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Stereoselective separation of β-adrenergic blocking agents containing two chiral centers by countercurrent chromatography

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Cited by 8 publications
(7 citation statements)
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“…Compounds 1 and 2 are ionizable organic base according to their chemical structures. It was found that they could be well enantioseparated by conventional countercurrent chromatography using di-n-hexyl L-tartrate and boric acid as chiral selector, as reported in our recent work [25]. A two-phase solvent system composed of chloroform/0.05 mol/L of acetate buffer containing 0.10 mol/L of boric acid (1:1, v/v) was used, in which 0.10 mol/L of di-n-hexyl L-tartrate was added in the organic phase as a chiral selector.…”
Section: Optimization Of Separation Conditionssupporting
confidence: 80%
See 1 more Smart Citation
“…Compounds 1 and 2 are ionizable organic base according to their chemical structures. It was found that they could be well enantioseparated by conventional countercurrent chromatography using di-n-hexyl L-tartrate and boric acid as chiral selector, as reported in our recent work [25]. A two-phase solvent system composed of chloroform/0.05 mol/L of acetate buffer containing 0.10 mol/L of boric acid (1:1, v/v) was used, in which 0.10 mol/L of di-n-hexyl L-tartrate was added in the organic phase as a chiral selector.…”
Section: Optimization Of Separation Conditionssupporting
confidence: 80%
“…Compared with traditional liquid chromatographic techniques, much smaller number of literatures about chiral separation by countercurrent chromatography was available due to its relatively low theoretical plates of separation column [20][21][22][23]. However, in the recent two years, increasing number of papers has been published on preparative enantioseparation by countercurrent chromatography [24][25][26][27][28][29][30][31][32][33]. Unfortunately, only five papers reporting successful chiral separations could be found in the literature when it comes to pH-zone-refining countercurrent chromatography since 1990s [34][35][36][37][38].…”
Section: Introductionmentioning
confidence: 99%
“…It is well-known that in many countries, these medicines are being sold as a racemic mixture, while the racemic form may be toxic or ballast to the patients. [6][7][8][9] These β-blockers have been separated by using various highperformance liquid chromatography (HPLC) methods, [10][11][12][13][14][15][16] but the methods reported in these papers are not eco-friendly, especially the use of toxic chemicals, high run time and a lot of use of manpower consumption. On the other hand, supercritical fluid chromatography (SFC) is a technique of low cost, less run time, higher column efficiency, and eco-friendly mobile phases that are the initial requirement of pharmaceutical industries.…”
Section: Introductionmentioning
confidence: 99%
“…Recycling elution mode was usually employed to improve enantioseparation in various chromatographic methods . In our very recent work, CCC was successfully applied for stereoselective separation of drugs and intermediates containing two chiral centers for the first time . In the present work, we want to report our recent work on stereoselective separation of four isomeric sertraline by an analytical countercurrent chromatographic apparatus designed in our lab, ( 1S, 4S ), ( 1R, 4R ), ( 1S, 4R ), and ( 1R, 4S )‐isomer, from the medicinal reaction mixture obtained during the synthesis of the antidepressant drug ( 1S, 4S )‐sertraline hydrochloride.…”
Section: Introductionmentioning
confidence: 99%