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Article: Chirally enshrouded 2,6-diarylbenzoic acids with two-fold symmetry

TitleChirally enshrouded 2,6-diarylbenzoic acids with two-fold symmetry
Authors
Issue Date1995
Citation
Tetrahedron Letters, 1995, v. 36, n. 46, p. 8403-8406 How to Cite?
AbstractThe synthesis and characterization of a new design of W-shaped chiral clefts with C2 symmetry is presented. The molecules are based on the 2,6-diarylbenzoic acid motif. A series of syn/anti isomers are discussed with respect to their symmetry, configurational stability, and suitability for the development of chiral materials. © 1995 Elsevier Science Ltd.
Persistent Identifierhttp://hdl.handle.net/10722/341040
ISSN
2023 Impact Factor: 1.5
2023 SCImago Journal Rankings: 0.323
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorChen, Chao Tsen-
dc.contributor.authorChadha, Raj-
dc.contributor.authorSiegel, Jay S.-
dc.contributor.authorHardcastle, Kenneth-
dc.date.accessioned2024-03-13T08:39:41Z-
dc.date.available2024-03-13T08:39:41Z-
dc.date.issued1995-
dc.identifier.citationTetrahedron Letters, 1995, v. 36, n. 46, p. 8403-8406-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10722/341040-
dc.description.abstractThe synthesis and characterization of a new design of W-shaped chiral clefts with C2 symmetry is presented. The molecules are based on the 2,6-diarylbenzoic acid motif. A series of syn/anti isomers are discussed with respect to their symmetry, configurational stability, and suitability for the development of chiral materials. © 1995 Elsevier Science Ltd.-
dc.languageeng-
dc.relation.ispartofTetrahedron Letters-
dc.titleChirally enshrouded 2,6-diarylbenzoic acids with two-fold symmetry-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/0040-4039(95)01800-W-
dc.identifier.scopuseid_2-s2.0-0028887053-
dc.identifier.volume36-
dc.identifier.issue46-
dc.identifier.spage8403-
dc.identifier.epage8406-
dc.identifier.isiWOS:A1995TD81600016-

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