Chemoenzymatic syntheses of (-)-1-deoxymannojirimycin (DMJ) and its naturally occurring 6- O -α-L-rhamnopyranosyl glycoside

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dc.contributor.authorBanwell, Martin
dc.contributor.authorMa, Xinghua
dc.contributor.authorAsano, Naoki
dc.contributor.authorIkeda, Kyoko
dc.contributor.authorLambert, John N
dc.date.accessioned2015-12-13T23:05:58Z
dc.date.available2015-12-13T23:05:58Z
dc.date.issued2003
dc.date.updated2015-12-12T08:03:10Z
dc.description.abstractNaturally occurring sugar mimetic alkaloids 1-deoxymannojirimycin (DMJ, 1) and 6-0-α-L-rhamnopyranosyl-DMJ were each prepared in a completely stereoselective manner from the cis-1,2-dihydrocatechol 3. The spectral and physical data derived proved an exce
dc.identifier.issn1477-0520
dc.identifier.urihttp://hdl.handle.net/1885/85804
dc.publisherRoyal Society of Chemistry
dc.sourceOrganic and Biomolecular Chemistry
dc.subjectKeywords: Agents; Benzene; Catalysts; Oxidation; Stereochemistry; Synthesis (chemical); Chemoenzymatic synthesis; Deoxymannojirimycin; Rhamnopyradnosyl glycoside; Organic compounds
dc.titleChemoenzymatic syntheses of (-)-1-deoxymannojirimycin (DMJ) and its naturally occurring 6- O -α-L-rhamnopyranosyl glycoside
dc.typeJournal article
local.bibliographicCitation.issue12
local.bibliographicCitation.lastpage2037
local.bibliographicCitation.startpage2035
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationMa, Xinghua, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationAsano, Naoki, Hokuriku University
local.contributor.affiliationIkeda, Kyoko, Hokuriku University
local.contributor.affiliationLambert, John N, Monash University
local.contributor.authoruidBanwell, Martin, u9500594
local.contributor.authoruidMa, Xinghua, u4002198
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor030499 - Medicinal and Biomolecular Chemistry not elsewhere classified
local.identifier.ariespublicationMigratedxPub14462
local.identifier.citationvolume1
local.identifier.doi10.1039/b304063a
local.identifier.scopusID2-s2.0-0142010050
local.type.statusPublished Version

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