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Studies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin A

dc.contributor.authorPaterson, Ianen
dc.contributor.authorMcLeod, Malcolm D.en
dc.date.accessioned2026-01-07T10:40:46Z
dc.date.available2026-01-07T10:40:46Z
dc.date.issued1995-12-04en
dc.description.abstractThe C19-C28 model fragment 2 of concanamycin A (1) was prepared by a Mukaiyama aldol reaction between silyl enol ether 11 and aldehyde 4 to give 7, followed by glycosylation with activated sugar 14 or 15.en
dc.description.statusPeer-revieweden
dc.format.extent4en
dc.identifier.issn0040-4039en
dc.identifier.scopus0028858247en
dc.identifier.urihttps://hdl.handle.net/1885/733803917
dc.language.isoenen
dc.sourceTetrahedron Lettersen
dc.titleStudies in macrolide synthesis: A sequential aldol/glycosylation approach to the synthesis of concanamycin Aen
dc.typeJournal articleen
dspace.entity.typePublicationen
local.bibliographicCitation.lastpage9068en
local.bibliographicCitation.startpage9065en
local.contributor.affiliationPaterson, Ian; University of Cambridgeen
local.contributor.affiliationMcLeod, Malcolm D.; University of Cambridgeen
local.identifier.citationvolume36en
local.identifier.doi10.1016/0040-4039(95)01913-3en
local.identifier.pureeb1de5e5-f6ad-40a7-b9d3-5e999908a70aen
local.identifier.urlhttps://www.scopus.com/pages/publications/0028858247en
local.type.statusPublisheden

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