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Article: Conformational diastereoisomerism in a chiral pretzelane

TitleConformational diastereoisomerism in a chiral pretzelane
Authors
Liu, YiVignon, Scott A.Zhang, XiyunHouk, K. N.Stoddart, J. Fraser
Issue Date2005
Citation
Chemical Communications, 2005, n. 31, p. 3927-3929 How to Cite?
DOI: http://dx.doi.org/10.1039/b507679j
AbstractThe introduction of a stereogenic center by a stereospecific synthesis into an optically active, donor-acceptor pretzelane, that exhibits helicity as well as fixed chirality, leads to a marked preference for one conformational diastereoisomer over the other in both acetone and dimethylsulfoxide that can be understood from computational models. © The Royal Society of Chemistry 2005.
Persistent Identifierhttp://hdl.handle.net/10722/333596
ISSN
1359-7345
2023 Impact Factor: 4.3
2023 SCImago Journal Rankings: 1.133
ISI Accession Number ID
WOS:000231131800010

 

DC FieldValueLanguage
dc.contributor.authorLiu, Yi-
dc.contributor.authorVignon, Scott A.-
dc.contributor.authorZhang, Xiyun-
dc.contributor.authorHouk, K. N.-
dc.contributor.authorStoddart, J. Fraser-
dc.date.accessioned2023-10-06T05:20:53Z-
dc.date.available2023-10-06T05:20:53Z-
dc.date.issued2005-
dc.identifier.citationChemical Communications, 2005, n. 31, p. 3927-3929-
dc.identifier.issn1359-7345-
dc.identifier.urihttp://hdl.handle.net/10722/333596-
dc.description.abstractThe introduction of a stereogenic center by a stereospecific synthesis into an optically active, donor-acceptor pretzelane, that exhibits helicity as well as fixed chirality, leads to a marked preference for one conformational diastereoisomer over the other in both acetone and dimethylsulfoxide that can be understood from computational models. © The Royal Society of Chemistry 2005.-
dc.languageeng-
dc.relation.ispartofChemical Communications-
dc.titleConformational diastereoisomerism in a chiral pretzelane-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1039/b507679j-
dc.identifier.scopuseid_2-s2.0-23944488533-
dc.identifier.issue31-
dc.identifier.spage3927-
dc.identifier.epage3929-
dc.identifier.isiWOS:000231131800010-

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