Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part

Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase in...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Helvetica chimica acta 2004-07, Vol.87 (7), p.1807-1824
Hauptverfasser: Yang, Guangbin, Mansourova, Madina, Hennig, Lothar, Findeisen, Matthias, Oehme, Ramona, Giesa, Sabine, Welzel, Peter
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1824
container_issue 7
container_start_page 1807
container_title Helvetica chimica acta
container_volume 87
creator Yang, Guangbin
Mansourova, Madina
Hennig, Lothar
Findeisen, Matthias
Oehme, Ramona
Giesa, Sabine
Welzel, Peter
description Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase inhibitors in detail and for preparing analogues with improved pharmacokinetic properties.
doi_str_mv 10.1002/hlca.200490161
format Article
fullrecord <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_hlca_200490161</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>HLCA200490161</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3251-a8f38243b8576ddd6654a580fa95c0011406f5661167482de58bbf94ba8afe583</originalsourceid><addsrcrecordid>eNqFkEtPwzAQhC0EEqVw5ew_kGInseMcQ-kDKeWhtpSb5cQ2NaRJZaeC8OtJG1Rx4zTa0Xy72gHgGqMBRsi_WRe5GPgIhTHCFJ-AHia-7_k0IqeghxBmHsLx6zm4cO4dIRTHKOqB73m9k0Y5WJWwXis4b8pWnGkNDe-MB0Up4cIaJ_J8LayRCialKKq3nTpEZpUqq02TmxImg3aSRptc1KYqHWy9ZWlqODosMd2B1GyNhE_C1pfgTIvCqatf7YPleLQYTr30cXI_TFIvD3yCPcF0wPwwyBiJqJSSUhIKwpAWMcnbt3CIqCaUYkyjkPlSEZZlOg4zwYRuh6APBt3e3FbOWaX51pqNsA3HiO-b4_vm-LG5Fog74NMUqvknzafpMPnLeh1rXK2-jqywH5xGQUT46mHC49nLajwOn_lt8APZaYEz</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part</title><source>Wiley Online Library All Journals</source><creator>Yang, Guangbin ; Mansourova, Madina ; Hennig, Lothar ; Findeisen, Matthias ; Oehme, Ramona ; Giesa, Sabine ; Welzel, Peter</creator><creatorcontrib>Yang, Guangbin ; Mansourova, Madina ; Hennig, Lothar ; Findeisen, Matthias ; Oehme, Ramona ; Giesa, Sabine ; Welzel, Peter</creatorcontrib><description>Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase inhibitors in detail and for preparing analogues with improved pharmacokinetic properties.</description><identifier>ISSN: 0018-019X</identifier><identifier>EISSN: 1522-2675</identifier><identifier>DOI: 10.1002/hlca.200490161</identifier><language>eng</language><publisher>Zürich: WILEY-VCH Verlag</publisher><ispartof>Helvetica chimica acta, 2004-07, Vol.87 (7), p.1807-1824</ispartof><rights>Copyright © 2004 Schweizerische Chemische Gesellschaft, Switzerland</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3251-a8f38243b8576ddd6654a580fa95c0011406f5661167482de58bbf94ba8afe583</citedby><cites>FETCH-LOGICAL-c3251-a8f38243b8576ddd6654a580fa95c0011406f5661167482de58bbf94ba8afe583</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhlca.200490161$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27923,27924,45574</link.rule.ids></links><search><creatorcontrib>Yang, Guangbin</creatorcontrib><creatorcontrib>Mansourova, Madina</creatorcontrib><creatorcontrib>Hennig, Lothar</creatorcontrib><creatorcontrib>Findeisen, Matthias</creatorcontrib><creatorcontrib>Oehme, Ramona</creatorcontrib><creatorcontrib>Giesa, Sabine</creatorcontrib><creatorcontrib>Welzel, Peter</creatorcontrib><title>Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part</title><title>Helvetica chimica acta</title><addtitle>HCA</addtitle><description>Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase inhibitors in detail and for preparing analogues with improved pharmacokinetic properties.</description><issn>0018-019X</issn><issn>1522-2675</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkEtPwzAQhC0EEqVw5ew_kGInseMcQ-kDKeWhtpSb5cQ2NaRJZaeC8OtJG1Rx4zTa0Xy72gHgGqMBRsi_WRe5GPgIhTHCFJ-AHia-7_k0IqeghxBmHsLx6zm4cO4dIRTHKOqB73m9k0Y5WJWwXis4b8pWnGkNDe-MB0Up4cIaJ_J8LayRCialKKq3nTpEZpUqq02TmxImg3aSRptc1KYqHWy9ZWlqODosMd2B1GyNhE_C1pfgTIvCqatf7YPleLQYTr30cXI_TFIvD3yCPcF0wPwwyBiJqJSSUhIKwpAWMcnbt3CIqCaUYkyjkPlSEZZlOg4zwYRuh6APBt3e3FbOWaX51pqNsA3HiO-b4_vm-LG5Fog74NMUqvknzafpMPnLeh1rXK2-jqywH5xGQUT46mHC49nLajwOn_lt8APZaYEz</recordid><startdate>200407</startdate><enddate>200407</enddate><creator>Yang, Guangbin</creator><creator>Mansourova, Madina</creator><creator>Hennig, Lothar</creator><creator>Findeisen, Matthias</creator><creator>Oehme, Ramona</creator><creator>Giesa, Sabine</creator><creator>Welzel, Peter</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>200407</creationdate><title>Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part</title><author>Yang, Guangbin ; Mansourova, Madina ; Hennig, Lothar ; Findeisen, Matthias ; Oehme, Ramona ; Giesa, Sabine ; Welzel, Peter</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3251-a8f38243b8576ddd6654a580fa95c0011406f5661167482de58bbf94ba8afe583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Guangbin</creatorcontrib><creatorcontrib>Mansourova, Madina</creatorcontrib><creatorcontrib>Hennig, Lothar</creatorcontrib><creatorcontrib>Findeisen, Matthias</creatorcontrib><creatorcontrib>Oehme, Ramona</creatorcontrib><creatorcontrib>Giesa, Sabine</creatorcontrib><creatorcontrib>Welzel, Peter</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><jtitle>Helvetica chimica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Guangbin</au><au>Mansourova, Madina</au><au>Hennig, Lothar</au><au>Findeisen, Matthias</au><au>Oehme, Ramona</au><au>Giesa, Sabine</au><au>Welzel, Peter</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part</atitle><jtitle>Helvetica chimica acta</jtitle><addtitle>HCA</addtitle><date>2004-07</date><risdate>2004</risdate><volume>87</volume><issue>7</issue><spage>1807</spage><epage>1824</epage><pages>1807-1824</pages><issn>0018-019X</issn><eissn>1522-2675</eissn><abstract>Routes allowing the synthesis of moenomycin analogues with one modified sugar component and with new lipid parts were developed (see 10c, 12c, 16b, and 20b in Schemes 2–4). It is anticipated that such analogues will be useful for studying the mode of action of the moenomycin‐type transglycosylase inhibitors in detail and for preparing analogues with improved pharmacokinetic properties.</abstract><cop>Zürich</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/hlca.200490161</doi><tpages>18</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0018-019X
ispartof Helvetica chimica acta, 2004-07, Vol.87 (7), p.1807-1824
issn 0018-019X
1522-2675
language eng
recordid cdi_crossref_primary_10_1002_hlca_200490161
source Wiley Online Library All Journals
title Studies on the Synthesis of Di- and Trisaccharide Analogues of Moenomycin A. Modifications in Unit E and in the Lipid Part
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T06%3A53%3A41IST&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=Studies%20on%20the%20Synthesis%20of%20Di-%20and%20Trisaccharide%20Analogues%20of%20Moenomycin%20A.%20Modifications%20in%20Unit%20E%20and%20in%20the%20Lipid%20Part&rft.jtitle=Helvetica%20chimica%20acta&rft.au=Yang,%20Guangbin&rft.date=2004-07&rft.volume=87&rft.issue=7&rft.spage=1807&rft.epage=1824&rft.pages=1807-1824&rft.issn=0018-019X&rft.eissn=1522-2675&rft_id=info:doi/10.1002/hlca.200490161&rft_dat=%3Cwiley_cross%3EHLCA200490161%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