2010
DOI: 10.1002/chir.20917
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Enantiomer self‐disproportionation and chiral stationary phase based selective chiral separation of organic compounds

Abstract: In modern chromatography, chiral stationary phase (CSP) and enantiomer selfdisproportionation (ESD) are new inventions of packing material offer a guarantee for a successful enantiomeric separation. All CSPs were synthesized by chemical bonding of the relevant organic moieties onto a porous parent silica material for the separation of various racemic mixtures whereas achiral silica matrix was used for separation of non-racemic mixtures in ESD. Our present study provides to establish an understanding on the ent… Show more

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Cited by 5 publications
(5 citation statements)
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References 27 publications
(44 reference statements)
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“…The sporadic reports till 1992 on such separations by liquid chromatography with both achiral phases were presented as a short review by Martens and Bhushan. 2 Since then there appeared a few more reports on enantioresolution of certain non racemic mixtures in achiral environment, these included some antihistamines, 3 binaphthol, 4,5 certain heterocyclic compounds 6 mandelic acid, 7,8 different uoro derivatives [9][10][11] and amine derivatives. 12 Martens and Bhushan 13 addressed the basic question and the concept 'why separation of one particular enantiomer (i.e., enantiomeric enrichment) should take place under achiral phase chromatography from the non-racemic mixture', discussed briey the technical terms used in literature and application of scientic terminology in the bounds of IUPAC while focusing on overlooked errors and scientic basis of separation in achiral environment during purication of enantiomeric mixtures in enantioselective synthesis.…”
Section: Introductionmentioning
confidence: 99%
“…The sporadic reports till 1992 on such separations by liquid chromatography with both achiral phases were presented as a short review by Martens and Bhushan. 2 Since then there appeared a few more reports on enantioresolution of certain non racemic mixtures in achiral environment, these included some antihistamines, 3 binaphthol, 4,5 certain heterocyclic compounds 6 mandelic acid, 7,8 different uoro derivatives [9][10][11] and amine derivatives. 12 Martens and Bhushan 13 addressed the basic question and the concept 'why separation of one particular enantiomer (i.e., enantiomeric enrichment) should take place under achiral phase chromatography from the non-racemic mixture', discussed briey the technical terms used in literature and application of scientic terminology in the bounds of IUPAC while focusing on overlooked errors and scientic basis of separation in achiral environment during purication of enantiomeric mixtures in enantioselective synthesis.…”
Section: Introductionmentioning
confidence: 99%
“…[27][28][29][30] However, the confinement effects have not been understood. This work could provide some fundamental insights.…”
Section: Confinement Effect Of Nanoporesmentioning
confidence: 99%
“…As is known, the confinement effect of nanopores can contribute to a superior catalytic behavior from catalyst confined in nanopores. [27][28][29][30] However, the confinement effects have not been understood. This work could provide some fundamental insights.…”
Section: Confinement Effect Of Nanoporesmentioning
confidence: 99%
“…(xiii) Enrichment of ( R )‐(−)‐mandelic acid with 28 % ee to 89.8 % ee using mesoporous silica M41S column (ground and sieved using 170 mesh size test sieves);, and…”
Section: Separation Of Enantiomers In the Absence Of Any External Somentioning
confidence: 99%