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Article: Synthesis and conformational behaviour of tetra-anthranilides

TitleSynthesis and conformational behaviour of tetra-anthranilides
Authors
Hoorfar, AlirezaDavid Ollis, W.Fraser Stoddart, J.Williams, David J.
Issue Date1980
Citation
Tetrahedron Letters, 1980, v. 21, n. 43, p. 4211-4214 How to Cite?
DOI: http://dx.doi.org/10.1016/S0040-4039(00)93691-8
AbstractThe tetra-anthranilide derivatives (5)-(7) have been synthesised. X-Ray crystallography shows that N,N′,N″-trimethyltetra-anthranilide (5) adopts a conformation with three trans - and one cis-amide linkages in the solid state. Dynamic 1H n.m.r. spectroscopy indicates that N-benzyl-N′,N″,N′″-trimethyltetra-anthranilide (7) exists as an interconverting ternary mixture of chiral non-planar conformational diastereoisomers in solution. © 1980.
Persistent Identifierhttp://hdl.handle.net/10722/333646
ISSN
0040-4039
2023 Impact Factor: 1.5
2023 SCImago Journal Rankings: 0.323
ISI Accession Number ID
WOS:A1980KP82200022

 

DC FieldValueLanguage
dc.contributor.authorHoorfar, Alireza-
dc.contributor.authorDavid Ollis, W.-
dc.contributor.authorFraser Stoddart, J.-
dc.contributor.authorWilliams, David J.-
dc.date.accessioned2023-10-06T05:21:17Z-
dc.date.available2023-10-06T05:21:17Z-
dc.date.issued1980-
dc.identifier.citationTetrahedron Letters, 1980, v. 21, n. 43, p. 4211-4214-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10722/333646-
dc.description.abstractThe tetra-anthranilide derivatives (5)-(7) have been synthesised. X-Ray crystallography shows that N,N′,N″-trimethyltetra-anthranilide (5) adopts a conformation with three trans - and one cis-amide linkages in the solid state. Dynamic 1H n.m.r. spectroscopy indicates that N-benzyl-N′,N″,N′″-trimethyltetra-anthranilide (7) exists as an interconverting ternary mixture of chiral non-planar conformational diastereoisomers in solution. © 1980.-
dc.languageeng-
dc.relation.ispartofTetrahedron Letters-
dc.titleSynthesis and conformational behaviour of tetra-anthranilides-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1016/S0040-4039(00)93691-8-
dc.identifier.scopuseid_2-s2.0-9444232334-
dc.identifier.volume21-
dc.identifier.issue43-
dc.identifier.spage4211-
dc.identifier.epage4214-
dc.identifier.isiWOS:A1980KP82200022-

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