Synthesis of a Model for C7−C13 of Lankamycin

A convenient method is reported for construction of the C7−C13 segment of the macrolide antiobiotic lankamycin.

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Organic letters 2000-01, Vol.2 (1), p.27-28
Hauptverfasser: Raimundo, Brian C, Heathcock, Clayton H
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 28
container_issue 1
container_start_page 27
container_title Organic letters
container_volume 2
creator Raimundo, Brian C
Heathcock, Clayton H
description A convenient method is reported for construction of the C7−C13 segment of the macrolide antiobiotic lankamycin.
doi_str_mv 10.1021/ol990376l
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_71147027</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>71147027</sourcerecordid><originalsourceid>FETCH-LOGICAL-a377t-e8e6e065c99f3bae5016c63a6d23e1b17ec7bb54938f4831c5e13bc93b853963</originalsourceid><addsrcrecordid>eNptkL1OwzAUhS0EoqUw8AIoC0gMob5xbMcjiviTihjobtnujUhJ4hI3Q9-gM4_Ik5AqVcXAdI-OPn3SPYRcAr0DmsDUV0pRJkV1RMbAExZLypPjQxZ0RM5CWFIKfaNOyQhoBmnC5JhM3zfN-gNDGSJfRCZ69QusosK3US5_tt85sF0_M82nqTeubM7JSWGqgBf7OyHzx4d5_hzP3p5e8vtZbJiU6xgzFEgFd0oVzBrkFIQTzIhFwhAsSHTSWp4qlhVpxsBxBGadYjbjTAk2ITeDdtX6rw7DWtdlcFhVpkHfBS0BUkkT2YO3A-haH0KLhV61ZW3ajQaqd-Powzg9e7WXdrbGxR9yWKMHrgfAuKCXvmub_sV_RL9xNWlH</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>71147027</pqid></control><display><type>article</type><title>Synthesis of a Model for C7−C13 of Lankamycin</title><source>MEDLINE</source><source>ACS Publications</source><creator>Raimundo, Brian C ; Heathcock, Clayton H</creator><creatorcontrib>Raimundo, Brian C ; Heathcock, Clayton H</creatorcontrib><description>A convenient method is reported for construction of the C7−C13 segment of the macrolide antiobiotic lankamycin.</description><identifier>ISSN: 1523-7060</identifier><identifier>EISSN: 1523-7052</identifier><identifier>DOI: 10.1021/ol990376l</identifier><identifier>PMID: 10814237</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Anti-Bacterial Agents - chemical synthesis ; Erythromycin - analogs &amp; derivatives ; Erythromycin - chemical synthesis ; Molecular Structure ; Streptomyces - chemistry</subject><ispartof>Organic letters, 2000-01, Vol.2 (1), p.27-28</ispartof><rights>Copyright © 2000 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a377t-e8e6e065c99f3bae5016c63a6d23e1b17ec7bb54938f4831c5e13bc93b853963</citedby><cites>FETCH-LOGICAL-a377t-e8e6e065c99f3bae5016c63a6d23e1b17ec7bb54938f4831c5e13bc93b853963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/ol990376l$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/ol990376l$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,777,781,2753,27058,27906,27907,56720,56770</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/10814237$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Raimundo, Brian C</creatorcontrib><creatorcontrib>Heathcock, Clayton H</creatorcontrib><title>Synthesis of a Model for C7−C13 of Lankamycin</title><title>Organic letters</title><addtitle>Org. Lett</addtitle><description>A convenient method is reported for construction of the C7−C13 segment of the macrolide antiobiotic lankamycin.</description><subject>Anti-Bacterial Agents - chemical synthesis</subject><subject>Erythromycin - analogs &amp; derivatives</subject><subject>Erythromycin - chemical synthesis</subject><subject>Molecular Structure</subject><subject>Streptomyces - chemistry</subject><issn>1523-7060</issn><issn>1523-7052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2000</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNptkL1OwzAUhS0EoqUw8AIoC0gMob5xbMcjiviTihjobtnujUhJ4hI3Q9-gM4_Ik5AqVcXAdI-OPn3SPYRcAr0DmsDUV0pRJkV1RMbAExZLypPjQxZ0RM5CWFIKfaNOyQhoBmnC5JhM3zfN-gNDGSJfRCZ69QusosK3US5_tt85sF0_M82nqTeubM7JSWGqgBf7OyHzx4d5_hzP3p5e8vtZbJiU6xgzFEgFd0oVzBrkFIQTzIhFwhAsSHTSWp4qlhVpxsBxBGadYjbjTAk2ITeDdtX6rw7DWtdlcFhVpkHfBS0BUkkT2YO3A-haH0KLhV61ZW3ajQaqd-Powzg9e7WXdrbGxR9yWKMHrgfAuKCXvmub_sV_RL9xNWlH</recordid><startdate>20000101</startdate><enddate>20000101</enddate><creator>Raimundo, Brian C</creator><creator>Heathcock, Clayton H</creator><general>American Chemical Society</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20000101</creationdate><title>Synthesis of a Model for C7−C13 of Lankamycin</title><author>Raimundo, Brian C ; Heathcock, Clayton H</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a377t-e8e6e065c99f3bae5016c63a6d23e1b17ec7bb54938f4831c5e13bc93b853963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2000</creationdate><topic>Anti-Bacterial Agents - chemical synthesis</topic><topic>Erythromycin - analogs &amp; derivatives</topic><topic>Erythromycin - chemical synthesis</topic><topic>Molecular Structure</topic><topic>Streptomyces - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Raimundo, Brian C</creatorcontrib><creatorcontrib>Heathcock, Clayton H</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Organic letters</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Raimundo, Brian C</au><au>Heathcock, Clayton H</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of a Model for C7−C13 of Lankamycin</atitle><jtitle>Organic letters</jtitle><addtitle>Org. Lett</addtitle><date>2000-01-01</date><risdate>2000</risdate><volume>2</volume><issue>1</issue><spage>27</spage><epage>28</epage><pages>27-28</pages><issn>1523-7060</issn><eissn>1523-7052</eissn><abstract>A convenient method is reported for construction of the C7−C13 segment of the macrolide antiobiotic lankamycin.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>10814237</pmid><doi>10.1021/ol990376l</doi><tpages>2</tpages></addata></record>
fulltext fulltext
identifier ISSN: 1523-7060
ispartof Organic letters, 2000-01, Vol.2 (1), p.27-28
issn 1523-7060
1523-7052
language eng
recordid cdi_proquest_miscellaneous_71147027
source MEDLINE; ACS Publications
subjects Anti-Bacterial Agents - chemical synthesis
Erythromycin - analogs & derivatives
Erythromycin - chemical synthesis
Molecular Structure
Streptomyces - chemistry
title Synthesis of a Model for C7−C13 of Lankamycin
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T09%3A41%3A53IST&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=Synthesis%20of%20a%20Model%20for%20C7%E2%88%92C13%20of%20Lankamycin&rft.jtitle=Organic%20letters&rft.au=Raimundo,%20Brian%20C&rft.date=2000-01-01&rft.volume=2&rft.issue=1&rft.spage=27&rft.epage=28&rft.pages=27-28&rft.issn=1523-7060&rft.eissn=1523-7052&rft_id=info:doi/10.1021/ol990376l&rft_dat=%3Cproquest_cross%3E71147027%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=71147027&rft_id=info:pmid/10814237&rfr_iscdi=true