Synthesis of azido analogues of medermycin

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Show simple item record Brimble, MA en Davey, RM en McLeod, MD en 2011-09-19T22:45:07Z en 2002 en
dc.identifier.citation SYNLETT 1318-1322 Aug 2002 en
dc.identifier.issn 0936-5214 en
dc.identifier.uri en
dc.description.abstract The synthesis of azido analogues 2a,2b of the pyrano-naphthoquinone antibiotic medermycin I has been achieved in eight steps from naphthol 8 and azido glycosyl sugar 7 in 9.3% overall yield. Key steps include the direct (BF3Et2O)-Et-. promoted C-glyc en
dc.language EN en
dc.relation.ispartofseries Synlett en
dc.rights Items in ResearchSpace are protected by copyright, with all rights reserved, unless otherwise indicated. Previously published items are made available in accordance with the copyright policy of the publisher. Details obtained from en
dc.rights.uri en
dc.subject pyranonaphthoquinone antibiotics en
dc.subject C-glycoside en
dc.subject amino sugar en
dc.subject Stille coupling en
dc.subject naphthoquinone en
dc.subject REAGENT en
dc.title Synthesis of azido analogues of medermycin en
dc.type Journal Article en
dc.identifier.doi 10.1055/s-2002-32955 en
pubs.issue 8 en
pubs.begin-page 1318 en
pubs.volume N/A en
dc.rights.holder Copyright: Georg Thieme Verlag Stuttgart, New York en
pubs.end-page 1322 en
dc.rights.accessrights en
pubs.subtype Article en
pubs.elements-id 4985 en Faculty of Science en Chemistry en Science Resrch Insts & Centres en Maurice Wilkins Centre (2010-2014) en
pubs.record-created-at-source-date 2010-09-01 en

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