ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis
ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option....
Gespeichert in:
| Veröffentlicht in: | ChemInform 2001-03, Vol.32 (13), p.no-no |
|---|---|
| Hauptverfasser: | , , , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | no |
|---|---|
| container_issue | 13 |
| container_start_page | no |
| container_title | ChemInform |
| container_volume | 32 |
| creator | Kitamoto, Dai Dieth, Serge Burger, Alain Tritsch, Denis Biellmann, Jean-Francois |
| description | ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option. |
| doi_str_mv | 10.1002/chin.200113194 |
| format | Article |
| fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_chin_200113194</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>CHIN200113194</sourcerecordid><originalsourceid>FETCH-LOGICAL-c1274-3f88bacf6fcd7e59a4e03ad1f08052b9a94b159d9c4d814de46065ddc193d5913</originalsourceid><addsrcrecordid>eNqFkN9q2zAYxcXYYFm3213rcoMokyzLsnYX3DYJlBbGyqA3QpZkrM2WgqSweI_VF9gb9JnmkFF2t6vv3_kd-A4A7wleEYyLT7p3flVgTAglonwBFoQVBSqqir8ECywoQZwJ_hq8Sen7rKe8Lhbgd9Pbcee7EEe4blOOSufPcDuZGI7TADcxHPYJqgwbRKHy5twSDkMHc2_hvfcqH6Ia4JVXPrsw2riE1me09rNHygqxpfhAyEdknPUW0afHJeFPj_MYBriOFt4dnXG_rIHtBJs-DDZlG-fbaa-ShV0MI_zSBxN00PqQoI1T7mPYh8Glt-BVp4Zk3_2tF-D--uprs0U3d5tds75BmhS8RLSr61bpruq04ZYJVVpMlSEdrjErWqFE2RImjNClqUlpbFnhihmjiaCGCUIvwOrsq-enUrSd3Ec3qjhJguUpfnmKXz7HPwPiDPx0g53-o5bNdnf7L4vOrJujOD6zKv6QFaecyW-3G9k8VNf0YXMpS_oHaWKbYg</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis</title><source>Wiley Journals</source><creator>Kitamoto, Dai ; Dieth, Serge ; Burger, Alain ; Tritsch, Denis ; Biellmann, Jean-Francois</creator><creatorcontrib>Kitamoto, Dai ; Dieth, Serge ; Burger, Alain ; Tritsch, Denis ; Biellmann, Jean-Francois</creatorcontrib><description>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</description><identifier>ISSN: 0931-7597</identifier><identifier>EISSN: 1522-2667</identifier><identifier>DOI: 10.1002/chin.200113194</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>biochemical syntheses ; biochemical syntheses, microbiological syntheses ; microbiological syntheses ; steroids</subject><ispartof>ChemInform, 2001-03, Vol.32 (13), p.no-no</ispartof><rights>Copyright © 2001 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c1274-3f88bacf6fcd7e59a4e03ad1f08052b9a94b159d9c4d814de46065ddc193d5913</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fchin.200113194$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fchin.200113194$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Kitamoto, Dai</creatorcontrib><creatorcontrib>Dieth, Serge</creatorcontrib><creatorcontrib>Burger, Alain</creatorcontrib><creatorcontrib>Tritsch, Denis</creatorcontrib><creatorcontrib>Biellmann, Jean-Francois</creatorcontrib><title>ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis</title><title>ChemInform</title><addtitle>ChemInform</addtitle><description>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</description><subject>biochemical syntheses</subject><subject>biochemical syntheses, microbiological syntheses</subject><subject>microbiological syntheses</subject><subject>steroids</subject><issn>0931-7597</issn><issn>1522-2667</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2001</creationdate><recordtype>article</recordtype><recordid>eNqFkN9q2zAYxcXYYFm3213rcoMokyzLsnYX3DYJlBbGyqA3QpZkrM2WgqSweI_VF9gb9JnmkFF2t6vv3_kd-A4A7wleEYyLT7p3flVgTAglonwBFoQVBSqqir8ECywoQZwJ_hq8Sen7rKe8Lhbgd9Pbcee7EEe4blOOSufPcDuZGI7TADcxHPYJqgwbRKHy5twSDkMHc2_hvfcqH6Ia4JVXPrsw2riE1me09rNHygqxpfhAyEdknPUW0afHJeFPj_MYBriOFt4dnXG_rIHtBJs-DDZlG-fbaa-ShV0MI_zSBxN00PqQoI1T7mPYh8Glt-BVp4Zk3_2tF-D--uprs0U3d5tds75BmhS8RLSr61bpruq04ZYJVVpMlSEdrjErWqFE2RImjNClqUlpbFnhihmjiaCGCUIvwOrsq-enUrSd3Ec3qjhJguUpfnmKXz7HPwPiDPx0g53-o5bNdnf7L4vOrJujOD6zKv6QFaecyW-3G9k8VNf0YXMpS_oHaWKbYg</recordid><startdate>20010327</startdate><enddate>20010327</enddate><creator>Kitamoto, Dai</creator><creator>Dieth, Serge</creator><creator>Burger, Alain</creator><creator>Tritsch, Denis</creator><creator>Biellmann, Jean-Francois</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20010327</creationdate><title>ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis</title><author>Kitamoto, Dai ; Dieth, Serge ; Burger, Alain ; Tritsch, Denis ; Biellmann, Jean-Francois</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1274-3f88bacf6fcd7e59a4e03ad1f08052b9a94b159d9c4d814de46065ddc193d5913</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2001</creationdate><topic>biochemical syntheses</topic><topic>biochemical syntheses, microbiological syntheses</topic><topic>microbiological syntheses</topic><topic>steroids</topic><toplevel>online_resources</toplevel><creatorcontrib>Kitamoto, Dai</creatorcontrib><creatorcontrib>Dieth, Serge</creatorcontrib><creatorcontrib>Burger, Alain</creatorcontrib><creatorcontrib>Tritsch, Denis</creatorcontrib><creatorcontrib>Biellmann, Jean-Francois</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>ChemInform</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kitamoto, Dai</au><au>Dieth, Serge</au><au>Burger, Alain</au><au>Tritsch, Denis</au><au>Biellmann, Jean-Francois</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis</atitle><jtitle>ChemInform</jtitle><addtitle>ChemInform</addtitle><date>2001-03-27</date><risdate>2001</risdate><volume>32</volume><issue>13</issue><spage>no</spage><epage>no</epage><pages>no-no</pages><issn>0931-7597</issn><eissn>1522-2667</eissn><abstract>ChemInform is a weekly ing Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable via the “References” option.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/chin.200113194</doi><tpages>1</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0931-7597 |
| ispartof | ChemInform, 2001-03, Vol.32 (13), p.no-no |
| issn | 0931-7597 1522-2667 |
| language | eng |
| recordid | cdi_crossref_primary_10_1002_chin_200113194 |
| source | Wiley Journals |
| subjects | biochemical syntheses biochemical syntheses, microbiological syntheses microbiological syntheses steroids |
| title | ChemInform Abstract: Hydroxyl Groups at C-3 and at C-17 of the Unnatural Enantiomer, ent-Androsta-5,9(11)-diene-3β,17β-diol Are Oxidized by Cholesterol Oxidase from Rhodococcus erythropolis |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-24T07%3A33%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ChemInform%20Abstract:%20Hydroxyl%20Groups%20at%20C-3%20and%20at%20C-17%20of%20the%20Unnatural%20Enantiomer,%20ent-Androsta-5,9(11)-diene-3%CE%B2,17%CE%B2-diol%20Are%20Oxidized%20by%20Cholesterol%20Oxidase%20from%20Rhodococcus%20erythropolis&rft.jtitle=ChemInform&rft.au=Kitamoto,%20Dai&rft.date=2001-03-27&rft.volume=32&rft.issue=13&rft.spage=no&rft.epage=no&rft.pages=no-no&rft.issn=0931-7597&rft.eissn=1522-2667&rft_id=info:doi/10.1002/chin.200113194&rft_dat=%3Cwiley_cross%3ECHIN200113194%3C/wiley_cross%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 |