π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin
Synthesis of an enantiomerically pure beta -lactam intermediate used in the preparation of the antibiotic (+)-thienamycin is described, by suitable elaboration of a functionalised pi -allytricarbonyliron complex.
Gespeichert in:
| Veröffentlicht in: | Journal of the Chemical Society. Chemical communications 1984 (8), p.494-496 |
|---|---|
| Hauptverfasser: | , , |
| Format: | Artikel |
| Sprache: | eng |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
| container_end_page | 496 |
|---|---|
| container_issue | 8 |
| container_start_page | 494 |
| container_title | Journal of the Chemical Society. Chemical communications |
| container_volume | |
| creator | HODGSON, S. T HOLLINSHEAD, D. M LEY, S. V |
| description | Synthesis of an enantiomerically pure beta -lactam intermediate used in the preparation of the antibiotic (+)-thienamycin is described, by suitable elaboration of a functionalised pi -allytricarbonyliron complex. |
| doi_str_mv | 10.1039/C39840000494 |
| format | Article |
| fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_13959619</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>13959619</sourcerecordid><originalsourceid>FETCH-LOGICAL-c317t-3c0ee87de5126f7287ce9dd9095105fe49796bbc3c6dd364704fd678dc8542d13</originalsourceid><addsrcrecordid>eNpNkEtOwzAYhL0AifLYcQAvEAJBwI6dOGZXVbykSmxgHTm2oxo5drBdiex6Jg4CVyKlFfBvfmnmm1kMAMcYXWFE-PWM8Iqi8SinO2CCUJ5nlJNyD-zH-DrqGFf5BKy-VtnU2sGmYKQIjXeDNcE7aIVM3mkofddb_a4jNA7GwaWFjibeQNH3dkwkM7LJw1H-c6Fvf4TPj2xdIzooXDKN8clIeHZxnqWF0U50gzTuEOy2wkZ9tP0H4OXu9nn2kM2f7h9n03kmCWYpIxJpXTGlC5yXLcsrJjVXiiNeYFS0mnLGy6aRRJZKkZIyRFtVskrJqqC5wuQAnG56--DfljqmujNRamuF034Za0x4wUvMR_ByA8rgYwy6rftgOhGGGqN6PW39f9oRP9n2iiiFbYNw0sTfDC8IqQpMvgFiIn25</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>13959619</pqid></control><display><type>article</type><title>π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin</title><source>Royal Society of Chemistry Journals Archive (1841-2007)</source><creator>HODGSON, S. T ; HOLLINSHEAD, D. M ; LEY, S. V</creator><creatorcontrib>HODGSON, S. T ; HOLLINSHEAD, D. M ; LEY, S. V</creatorcontrib><description>Synthesis of an enantiomerically pure beta -lactam intermediate used in the preparation of the antibiotic (+)-thienamycin is described, by suitable elaboration of a functionalised pi -allytricarbonyliron complex.</description><identifier>ISSN: 0022-4936</identifier><identifier>DOI: 10.1039/C39840000494</identifier><identifier>CODEN: JCCCAT</identifier><language>eng</language><publisher>Cambridge: Royal Society of Chemistry</publisher><subject>Chemistry ; Exact sciences and technology ; Heterocyclic compounds ; Heterocyclic compounds with only one n hetero atom and condensed derivatives ; Organic chemistry ; peptide synthesis ; Preparations and properties ; thienamycin</subject><ispartof>Journal of the Chemical Society. Chemical communications, 1984 (8), p.494-496</ispartof><rights>1984 INIST-CNRS</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c317t-3c0ee87de5126f7287ce9dd9095105fe49796bbc3c6dd364704fd678dc8542d13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,2831,4024,27923,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=9533851$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>HODGSON, S. T</creatorcontrib><creatorcontrib>HOLLINSHEAD, D. M</creatorcontrib><creatorcontrib>LEY, S. V</creatorcontrib><title>π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin</title><title>Journal of the Chemical Society. Chemical communications</title><description>Synthesis of an enantiomerically pure beta -lactam intermediate used in the preparation of the antibiotic (+)-thienamycin is described, by suitable elaboration of a functionalised pi -allytricarbonyliron complex.</description><subject>Chemistry</subject><subject>Exact sciences and technology</subject><subject>Heterocyclic compounds</subject><subject>Heterocyclic compounds with only one n hetero atom and condensed derivatives</subject><subject>Organic chemistry</subject><subject>peptide synthesis</subject><subject>Preparations and properties</subject><subject>thienamycin</subject><issn>0022-4936</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1984</creationdate><recordtype>article</recordtype><recordid>eNpNkEtOwzAYhL0AifLYcQAvEAJBwI6dOGZXVbykSmxgHTm2oxo5drBdiex6Jg4CVyKlFfBvfmnmm1kMAMcYXWFE-PWM8Iqi8SinO2CCUJ5nlJNyD-zH-DrqGFf5BKy-VtnU2sGmYKQIjXeDNcE7aIVM3mkofddb_a4jNA7GwaWFjibeQNH3dkwkM7LJw1H-c6Fvf4TPj2xdIzooXDKN8clIeHZxnqWF0U50gzTuEOy2wkZ9tP0H4OXu9nn2kM2f7h9n03kmCWYpIxJpXTGlC5yXLcsrJjVXiiNeYFS0mnLGy6aRRJZKkZIyRFtVskrJqqC5wuQAnG56--DfljqmujNRamuF034Za0x4wUvMR_ByA8rgYwy6rftgOhGGGqN6PW39f9oRP9n2iiiFbYNw0sTfDC8IqQpMvgFiIn25</recordid><startdate>1984</startdate><enddate>1984</enddate><creator>HODGSON, S. T</creator><creator>HOLLINSHEAD, D. M</creator><creator>LEY, S. V</creator><general>Royal Society of Chemistry</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>1984</creationdate><title>π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin</title><author>HODGSON, S. T ; HOLLINSHEAD, D. M ; LEY, S. V</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c317t-3c0ee87de5126f7287ce9dd9095105fe49796bbc3c6dd364704fd678dc8542d13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1984</creationdate><topic>Chemistry</topic><topic>Exact sciences and technology</topic><topic>Heterocyclic compounds</topic><topic>Heterocyclic compounds with only one n hetero atom and condensed derivatives</topic><topic>Organic chemistry</topic><topic>peptide synthesis</topic><topic>Preparations and properties</topic><topic>thienamycin</topic><toplevel>online_resources</toplevel><creatorcontrib>HODGSON, S. T</creatorcontrib><creatorcontrib>HOLLINSHEAD, D. M</creatorcontrib><creatorcontrib>LEY, S. V</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>Journal of the Chemical Society. Chemical communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>HODGSON, S. T</au><au>HOLLINSHEAD, D. M</au><au>LEY, S. V</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin</atitle><jtitle>Journal of the Chemical Society. Chemical communications</jtitle><date>1984</date><risdate>1984</risdate><issue>8</issue><spage>494</spage><epage>496</epage><pages>494-496</pages><issn>0022-4936</issn><coden>JCCCAT</coden><abstract>Synthesis of an enantiomerically pure beta -lactam intermediate used in the preparation of the antibiotic (+)-thienamycin is described, by suitable elaboration of a functionalised pi -allytricarbonyliron complex.</abstract><cop>Cambridge</cop><pub>Royal Society of Chemistry</pub><doi>10.1039/C39840000494</doi><tpages>3</tpages></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0022-4936 |
| ispartof | Journal of the Chemical Society. Chemical communications, 1984 (8), p.494-496 |
| issn | 0022-4936 |
| language | eng |
| recordid | cdi_proquest_miscellaneous_13959619 |
| source | Royal Society of Chemistry Journals Archive (1841-2007) |
| subjects | Chemistry Exact sciences and technology Heterocyclic compounds Heterocyclic compounds with only one n hetero atom and condensed derivatives Organic chemistry peptide synthesis Preparations and properties thienamycin |
| title | π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin |
| url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-19T10%3A10%3A01IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=%CF%80-Allyltricarbonyliron%20lactone%20complexes%20in%20synthesis:%20application%20to%20the%20synthesis%20of%20the%20%CE%B2-lactam%20antibiotic%20(+)-thienamycin&rft.jtitle=Journal%20of%20the%20Chemical%20Society.%20Chemical%20communications&rft.au=HODGSON,%20S.%20T&rft.date=1984&rft.issue=8&rft.spage=494&rft.epage=496&rft.pages=494-496&rft.issn=0022-4936&rft.coden=JCCCAT&rft_id=info:doi/10.1039/C39840000494&rft_dat=%3Cproquest_cross%3E13959619%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=13959619&rft_id=info:pmid/&rfr_iscdi=true |