Stille/Diels-Alder reaction sequences: diversity-oriented access to novel steroids

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dc.contributor.authorSunnemann, Hans Wolf
dc.contributor.authorHofmeister, Anja
dc.contributor.authorMagull, Jörg
dc.contributor.authorBanwell, Martin
dc.contributor.authorde Meijere, Armin
dc.date.accessioned2015-12-07T22:40:48Z
dc.date.issued2007
dc.date.updated2015-12-07T10:54:29Z
dc.description.abstractAn efficient, diversity-oriented approach to novel steroid analogues possessing a C-5β configuration begins with the Stille cross-coupling of enantiomerically pure cycloalkenylstannane trans-2 and enol triflate 3. The resulting diene trans-4 engages in D
dc.identifier.issn1523-7060
dc.identifier.urihttp://hdl.handle.net/1885/24028
dc.publisherAmerican Chemical Society
dc.sourceOrganic Letters
dc.subjectKeywords: alkadiene; cross linking reagent; cycloalkane derivative; mesylic acid derivative; organometallic compound; stannane; steroid; tin derivative; trifluoromethanesulfonic acid; unclassified drug; article; chemical model; chemistry; cyclization; stereoisomeri
dc.titleStille/Diels-Alder reaction sequences: diversity-oriented access to novel steroids
dc.typeJournal article
local.bibliographicCitation.issue3
local.bibliographicCitation.lastpage520
local.bibliographicCitation.startpage517
local.contributor.affiliationSunnemann, Hans Wolf, University of Gottingen
local.contributor.affiliationHofmeister, Anja, University of Gottingen
local.contributor.affiliationMagull, Jörg, University of Gottingen
local.contributor.affiliationBanwell, Martin, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationde Meijere, Armin, University of Gottingen
local.contributor.authoruidBanwell, Martin, u9500594
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030503 - Organic Chemical Synthesis
local.identifier.ariespublicationu4005981xPUB30
local.identifier.citationvolume9
local.identifier.doi10.1021/ol062878m
local.identifier.scopusID2-s2.0-33847018090
local.type.statusPublished Version

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