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dc.contributor.authorParchinsky, Vladislav
dc.contributor.authorShumsky, Alexei
dc.contributor.authorKrasavin, Mikhail
dc.date.accessioned2017-05-03T15:58:31Z
dc.date.available2017-05-03T15:58:31Z
dc.date.issued2011
dc.date.modified2012-06-11T22:59:08Z
dc.identifier.issn00404039
dc.identifier.doi10.1016/j.tetlet.2011.10.125
dc.identifier.urihttp://hdl.handle.net/10072/44753
dc.description.abstractNovel symmetrically and unsymmetrically disubstituted 1-azaadamantanes were prepared as a single, chiral diastereomer via double microwave-assisted aza-Prins cyclization in one-pot or sequential reaction format.
dc.description.peerreviewedYes
dc.description.publicationstatusYes
dc.format.extent81576 bytes
dc.format.mimetypeapplication/pdf
dc.languageEnglish
dc.language.isoeng
dc.publisherElsevier
dc.publisher.placeUnited Kingdom
dc.relation.ispartofstudentpublicationN
dc.relation.ispartofpagefrom7161
dc.relation.ispartofpageto7163
dc.relation.ispartofissue52
dc.relation.ispartofjournalTetrahedron Letters
dc.relation.ispartofvolume52
dc.rights.retentionN
dc.subject.fieldofresearchOrganic Chemical Synthesis
dc.subject.fieldofresearchMedicinal and Biomolecular Chemistry
dc.subject.fieldofresearchOrganic Chemistry
dc.subject.fieldofresearchcode030503
dc.subject.fieldofresearchcode0304
dc.subject.fieldofresearchcode0305
dc.titleMicrowave-assisted aza-Prins reaction. Part 2: straightforward access to 2,6-disubstituted 1-azaadamantanes
dc.typeJournal article
dc.type.descriptionC1 - Articles
dc.type.codeC - Journal Articles
gro.rights.copyright© 2011 Elsevier. This is the author-manuscript version of this paper. Reproduced in accordance with the copyright policy of the publisher. Please refer to the journal's website for access to the definitive, published version.
gro.date.issued2011
gro.hasfulltextFull Text
gro.griffith.authorKrasavin, Mikhail


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