Crystal Structures of L -(R)-Cysteine-Mandelic Acid Diastereomers
The crystal structures of the title compounds, L -(R)-cysteine- D -(R)-mandelic acid, (I), and L -(R)-cysteine- L -(S)-mandelic acid, (II), have been determined. The structures show a common fashion in molecular recognition in hydrophilic layers, except for the arrangement of phenyl rings against me...
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Veröffentlicht in: | Analytical Sciences ; X-ray Structure and Analysis Online 2005, Vol.21, pp.x175-x176 |
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creator | FUJII, Isao BABA, Hiroyuki TAKAHASHI, Yukio |
description | The crystal structures of the title compounds, L -(R)-cysteine- D -(R)-mandelic acid, (I), and L -(R)-cysteine- L -(S)-mandelic acid, (II), have been determined. The structures show a common fashion in molecular recognition in hydrophilic layers, except for the arrangement of phenyl rings against mercapto groups. Crystallographic and physicochemical experiments have clarified the entropic and enthalpic advantage of (II) than (I). It plays a key role in the optical separation of mandelic acid with chiral L -cysteine. |
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The structures show a common fashion in molecular recognition in hydrophilic layers, except for the arrangement of phenyl rings against mercapto groups. Crystallographic and physicochemical experiments have clarified the entropic and enthalpic advantage of (II) than (I). It plays a key role in the optical separation of mandelic acid with chiral L -cysteine.</description><identifier>ISSN: 1348-2238</identifier><identifier>EISSN: 1348-2238</identifier><identifier>EISSN: 1883-3578</identifier><identifier>DOI: 10.2116/analscix.21.x175</identifier><language>eng</language><publisher>Tokyo: The Japan Society for Analytical Chemistry</publisher><ispartof>Analytical Sciences: X-ray Structure Analysis Online, 2005, Vol.21, pp.x175-x176</ispartof><rights>2005 by The Japan Society for Analytical Chemistry</rights><rights>Copyright Japan Science and Technology Agency 2005</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4575-6fd185061a386208a654b1be1a9c710f37df86021c19ccd7ee1b88070670b3733</citedby><cites>FETCH-LOGICAL-c4575-6fd185061a386208a654b1be1a9c710f37df86021c19ccd7ee1b88070670b3733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,1884,4025,27928,27929,27930</link.rule.ids></links><search><creatorcontrib>FUJII, Isao</creatorcontrib><creatorcontrib>BABA, Hiroyuki</creatorcontrib><creatorcontrib>TAKAHASHI, Yukio</creatorcontrib><title>Crystal Structures of L -(R)-Cysteine-Mandelic Acid Diastereomers</title><title>Analytical Sciences ; X-ray Structure and Analysis Online</title><description>The crystal structures of the title compounds, L -(R)-cysteine- D -(R)-mandelic acid, (I), and L -(R)-cysteine- L -(S)-mandelic acid, (II), have been determined. 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The structures show a common fashion in molecular recognition in hydrophilic layers, except for the arrangement of phenyl rings against mercapto groups. Crystallographic and physicochemical experiments have clarified the entropic and enthalpic advantage of (II) than (I). It plays a key role in the optical separation of mandelic acid with chiral L -cysteine.</abstract><cop>Tokyo</cop><pub>The Japan Society for Analytical Chemistry</pub><doi>10.2116/analscix.21.x175</doi><oa>free_for_read</oa></addata></record> |
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title | Crystal Structures of L -(R)-Cysteine-Mandelic Acid Diastereomers |
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