The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]

The reaction of DL-phenylalanine and [Cr(L-phe) 2 (NCS)-(OH 2 )](phe = phenylalaninato) in ethanolic solution led to the selective formation of [Cr(L-phe) 2 (D-phe-N)(OH 2 )] and fac-(-) 5 4 8 [Cr(L-phe) 3 ], that is, [Cr(L-phe) 2 (D-phe - N)(OH 2 )] was obtained during the heating and [Cr(L-phe) 3...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Synthesis and reactivity in inorganic and metal-organic chemistry 1989-12, Vol.19 (10), p.1085-1091
Hauptverfasser: Oki, Hisaya, Enomae, Masami, Yoshimura, Yoshitake
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1091
container_issue 10
container_start_page 1085
container_title Synthesis and reactivity in inorganic and metal-organic chemistry
container_volume 19
creator Oki, Hisaya
Enomae, Masami
Yoshimura, Yoshitake
description The reaction of DL-phenylalanine and [Cr(L-phe) 2 (NCS)-(OH 2 )](phe = phenylalaninato) in ethanolic solution led to the selective formation of [Cr(L-phe) 2 (D-phe-N)(OH 2 )] and fac-(-) 5 4 8 [Cr(L-phe) 3 ], that is, [Cr(L-phe) 2 (D-phe - N)(OH 2 )] was obtained during the heating and [Cr(L-phe) 3 ] was yielded from the filtrate. In the case of L- or D-phenylalanine, fac-(-) 5 4 6 [Cr(L-phe) 3 ] and [Cr(L-phe) 2 (D-phe-N)(OH 2 )] were only obtained, respectively. By using this procedure, the possibility of the optical resolution of DL-phenylalanine was confirmed.
doi_str_mv 10.1080/00945718908048118
format Article
fullrecord <record><control><sourceid>crossref_infor</sourceid><recordid>TN_cdi_crossref_primary_10_1080_00945718908048118</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>10_1080_00945718908048118</sourcerecordid><originalsourceid>FETCH-LOGICAL-c296t-dbe93ffe516745afdcbd1602c1ddeef2bbc570efc27fbabebeedb930670b13873</originalsourceid><addsrcrecordid>eNp1kEtLAzEUhYMoWKs_wN0s20U0j3mCGxkfFQZbtOJCZMjjhkbipCQjMv_eKXUnri7nnvsduAehc0ouKCnJJSFVmhW0rEaRlpSWB2hCM84wS1NyiCY7H48H6TE6ifGDEFpSzibodb2BZOVjtNI62w-JN0k_rpbb3irhkieI3n311nc756bBqw10gxNOdLaDRA7JWx1mDd5uYM5mj_XzfLZcsPn7KToywkU4-51T9HJ3u64XuFneP9TXDVasynusJVTcGMhoXqSZMFpJTXPCFNUawDApVVYQMIoVRgoJEkDLipO8IJLysuBTRPe5KoxPBDDtNthPEYaWknbXTPunmZG52jO2Mz58im8fnG57MTgfTBCdsrHl_-M_fh9ovQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]</title><source>Taylor &amp; Francis E-Journals</source><creator>Oki, Hisaya ; Enomae, Masami ; Yoshimura, Yoshitake</creator><creatorcontrib>Oki, Hisaya ; Enomae, Masami ; Yoshimura, Yoshitake</creatorcontrib><description>The reaction of DL-phenylalanine and [Cr(L-phe) 2 (NCS)-(OH 2 )](phe = phenylalaninato) in ethanolic solution led to the selective formation of [Cr(L-phe) 2 (D-phe-N)(OH 2 )] and fac-(-) 5 4 8 [Cr(L-phe) 3 ], that is, [Cr(L-phe) 2 (D-phe - N)(OH 2 )] was obtained during the heating and [Cr(L-phe) 3 ] was yielded from the filtrate. In the case of L- or D-phenylalanine, fac-(-) 5 4 6 [Cr(L-phe) 3 ] and [Cr(L-phe) 2 (D-phe-N)(OH 2 )] were only obtained, respectively. By using this procedure, the possibility of the optical resolution of DL-phenylalanine was confirmed.</description><identifier>ISSN: 0094-5714</identifier><identifier>EISSN: 1532-2440</identifier><identifier>DOI: 10.1080/00945718908048118</identifier><language>eng</language><publisher>Taylor &amp; Francis Group</publisher><ispartof>Synthesis and reactivity in inorganic and metal-organic chemistry, 1989-12, Vol.19 (10), p.1085-1091</ispartof><rights>Copyright Taylor &amp; Francis Group, LLC 1989</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c296t-dbe93ffe516745afdcbd1602c1ddeef2bbc570efc27fbabebeedb930670b13873</citedby><cites>FETCH-LOGICAL-c296t-dbe93ffe516745afdcbd1602c1ddeef2bbc570efc27fbabebeedb930670b13873</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00945718908048118$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00945718908048118$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27903,27904,59623,60412</link.rule.ids></links><search><creatorcontrib>Oki, Hisaya</creatorcontrib><creatorcontrib>Enomae, Masami</creatorcontrib><creatorcontrib>Yoshimura, Yoshitake</creatorcontrib><title>The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]</title><title>Synthesis and reactivity in inorganic and metal-organic chemistry</title><description>The reaction of DL-phenylalanine and [Cr(L-phe) 2 (NCS)-(OH 2 )](phe = phenylalaninato) in ethanolic solution led to the selective formation of [Cr(L-phe) 2 (D-phe-N)(OH 2 )] and fac-(-) 5 4 8 [Cr(L-phe) 3 ], that is, [Cr(L-phe) 2 (D-phe - N)(OH 2 )] was obtained during the heating and [Cr(L-phe) 3 ] was yielded from the filtrate. In the case of L- or D-phenylalanine, fac-(-) 5 4 6 [Cr(L-phe) 3 ] and [Cr(L-phe) 2 (D-phe-N)(OH 2 )] were only obtained, respectively. By using this procedure, the possibility of the optical resolution of DL-phenylalanine was confirmed.</description><issn>0094-5714</issn><issn>1532-2440</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><recordid>eNp1kEtLAzEUhYMoWKs_wN0s20U0j3mCGxkfFQZbtOJCZMjjhkbipCQjMv_eKXUnri7nnvsduAehc0ouKCnJJSFVmhW0rEaRlpSWB2hCM84wS1NyiCY7H48H6TE6ifGDEFpSzibodb2BZOVjtNI62w-JN0k_rpbb3irhkieI3n311nc756bBqw10gxNOdLaDRA7JWx1mDd5uYM5mj_XzfLZcsPn7KToywkU4-51T9HJ3u64XuFneP9TXDVasynusJVTcGMhoXqSZMFpJTXPCFNUawDApVVYQMIoVRgoJEkDLipO8IJLysuBTRPe5KoxPBDDtNthPEYaWknbXTPunmZG52jO2Mz58im8fnG57MTgfTBCdsrHl_-M_fh9ovQ</recordid><startdate>19891201</startdate><enddate>19891201</enddate><creator>Oki, Hisaya</creator><creator>Enomae, Masami</creator><creator>Yoshimura, Yoshitake</creator><general>Taylor &amp; Francis Group</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>19891201</creationdate><title>The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]</title><author>Oki, Hisaya ; Enomae, Masami ; Yoshimura, Yoshitake</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c296t-dbe93ffe516745afdcbd1602c1ddeef2bbc570efc27fbabebeedb930670b13873</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><toplevel>online_resources</toplevel><creatorcontrib>Oki, Hisaya</creatorcontrib><creatorcontrib>Enomae, Masami</creatorcontrib><creatorcontrib>Yoshimura, Yoshitake</creatorcontrib><collection>CrossRef</collection><jtitle>Synthesis and reactivity in inorganic and metal-organic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oki, Hisaya</au><au>Enomae, Masami</au><au>Yoshimura, Yoshitake</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]</atitle><jtitle>Synthesis and reactivity in inorganic and metal-organic chemistry</jtitle><date>1989-12-01</date><risdate>1989</risdate><volume>19</volume><issue>10</issue><spage>1085</spage><epage>1091</epage><pages>1085-1091</pages><issn>0094-5714</issn><eissn>1532-2440</eissn><abstract>The reaction of DL-phenylalanine and [Cr(L-phe) 2 (NCS)-(OH 2 )](phe = phenylalaninato) in ethanolic solution led to the selective formation of [Cr(L-phe) 2 (D-phe-N)(OH 2 )] and fac-(-) 5 4 8 [Cr(L-phe) 3 ], that is, [Cr(L-phe) 2 (D-phe - N)(OH 2 )] was obtained during the heating and [Cr(L-phe) 3 ] was yielded from the filtrate. In the case of L- or D-phenylalanine, fac-(-) 5 4 6 [Cr(L-phe) 3 ] and [Cr(L-phe) 2 (D-phe-N)(OH 2 )] were only obtained, respectively. By using this procedure, the possibility of the optical resolution of DL-phenylalanine was confirmed.</abstract><pub>Taylor &amp; Francis Group</pub><doi>10.1080/00945718908048118</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0094-5714
ispartof Synthesis and reactivity in inorganic and metal-organic chemistry, 1989-12, Vol.19 (10), p.1085-1091
issn 0094-5714
1532-2440
language eng
recordid cdi_crossref_primary_10_1080_00945718908048118
source Taylor & Francis E-Journals
title The Possibility of the Optical Resolution of DL-Phenylalanine by [Cr(L-phe)2(NCS)(OH2)]
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T19%3A52%3A42IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-crossref_infor&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20Possibility%20of%20the%20Optical%20Resolution%20of%20DL-Phenylalanine%20by%20%5BCr(L-phe)2(NCS)(OH2)%5D&rft.jtitle=Synthesis%20and%20reactivity%20in%20inorganic%20and%20metal-organic%20chemistry&rft.au=Oki,%20Hisaya&rft.date=1989-12-01&rft.volume=19&rft.issue=10&rft.spage=1085&rft.epage=1091&rft.pages=1085-1091&rft.issn=0094-5714&rft.eissn=1532-2440&rft_id=info:doi/10.1080/00945718908048118&rft_dat=%3Ccrossref_infor%3E10_1080_00945718908048118%3C/crossref_infor%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true