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dc.contributor.authorLoughlin, WA
dc.contributor.authorRowen, CC
dc.contributor.authorHealy, PC
dc.date.accessioned2017-05-03T12:22:30Z
dc.date.available2017-05-03T12:22:30Z
dc.date.issued2005
dc.date.modified2009-08-25T03:44:38Z
dc.identifier.issn0039-7881
dc.identifier.doi10.1055/s-2005-869993
dc.identifier.urihttp://hdl.handle.net/10072/4957
dc.description.abstractBicyclo[4.2.0]octanols can be obtained from the reaction of phenyl vinyl sulfoxide and the lithium enolate of cyclohexanone under controlled conditions. Diversion to alkylation or Michael-Michael-ring closure was observed when alternative vinyl electrophiles were used. Novel bicyclic disulfones and hydroxyhexahydronaphthalenes were isolated. The use of a vinyl sulfoxide electrophile is crucial to the formation of bicyclo[4.2.0]octanols from simple ketones.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.languageEnglish
dc.language.isoeng
dc.publisherGeorg Thieme Verlag
dc.publisher.placeStuttgart, Germany
dc.publisher.urihttp://www.thieme-chemistry.com/en/products/journals/synthesis.html
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom2220
dc.relation.ispartofpageto2226
dc.relation.ispartofjournalSynthesis: journal of synthetic organic chemistry
dc.relation.ispartofvolume13
dc.rights.retentionY
dc.subject.fieldofresearchAnalytical chemistry
dc.subject.fieldofresearchOrganic chemistry
dc.subject.fieldofresearchcode3401
dc.subject.fieldofresearchcode3405
dc.titleDiversion from bicyclo[4.2.0]octanol formation through the use of vinyl electrophiles
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.rights.copyright© 2005 Georg Thieme Verlag. Please refer to the journal link for access to the definitive, published version.
gro.date.issued2005
gro.hasfulltextNo Full Text
gro.griffith.authorHealy, Peter C.
gro.griffith.authorLoughlin, Wendy A.


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