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- Publisher Website: 10.1039/b507679j
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Article: Conformational diastereoisomerism in a chiral pretzelane
Title | Conformational diastereoisomerism in a chiral pretzelane |
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Authors | |
Issue Date | 2005 |
Citation | Chemical Communications, 2005, n. 31, p. 3927-3929 How to Cite? |
Abstract | The 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 Identifier | http://hdl.handle.net/10722/333596 |
ISSN | 2023 Impact Factor: 4.3 2023 SCImago Journal Rankings: 1.133 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Liu, Yi | - |
dc.contributor.author | Vignon, Scott A. | - |
dc.contributor.author | Zhang, Xiyun | - |
dc.contributor.author | Houk, K. N. | - |
dc.contributor.author | Stoddart, J. Fraser | - |
dc.date.accessioned | 2023-10-06T05:20:53Z | - |
dc.date.available | 2023-10-06T05:20:53Z | - |
dc.date.issued | 2005 | - |
dc.identifier.citation | Chemical Communications, 2005, n. 31, p. 3927-3929 | - |
dc.identifier.issn | 1359-7345 | - |
dc.identifier.uri | http://hdl.handle.net/10722/333596 | - |
dc.description.abstract | The 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.language | eng | - |
dc.relation.ispartof | Chemical Communications | - |
dc.title | Conformational diastereoisomerism in a chiral pretzelane | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1039/b507679j | - |
dc.identifier.scopus | eid_2-s2.0-23944488533 | - |
dc.identifier.issue | 31 | - |
dc.identifier.spage | 3927 | - |
dc.identifier.epage | 3929 | - |
dc.identifier.isi | WOS:000231131800010 | - |