File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: The structure-directed synthesis of cyclacene and polyacene derivatives

TitleThe structure-directed synthesis of cyclacene and polyacene derivatives
Authors
Issue Date1993
Citation
Pure and Applied Chemistry, 1993, v. 65, n. 1, p. 119-125 How to Cite?
AbstractThe treble diastereoselectivities exhibited by Diels-Alder reactions which occur between diene and dienophilic components associated with bicyclic systems have been employed in the stepwise construction of compounds with molecular architectures that resemble cups and cages. These macropolycyclic compounds are potential synthetic precursors of novel hydrocarbons composed of [a,d]-fused and [a,c]-fused six-membered rings. The hydrocarbons themselves are of considerable importance in investigating the behaviour of π-electrons in highly-conjugated cyclic systems and in understanding the influence upon the aromaticity and antiaromaticity of benzenoid and fused benzenoid rings that are obliged to become bent. © 1993 IUPAC
Persistent Identifierhttp://hdl.handle.net/10722/332290
ISSN
2023 Impact Factor: 2.0
2023 SCImago Journal Rankings: 0.435
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorGirreser, Ulrich-
dc.contributor.authorGiuffrida, Daniele-
dc.contributor.authorPhilp, Douglas-
dc.contributor.authorStoddart, J. Fraser-
dc.contributor.authorKohnke, Franz H.-
dc.contributor.authorMathias, John P.-
dc.date.accessioned2023-10-06T05:10:19Z-
dc.date.available2023-10-06T05:10:19Z-
dc.date.issued1993-
dc.identifier.citationPure and Applied Chemistry, 1993, v. 65, n. 1, p. 119-125-
dc.identifier.issn0033-4545-
dc.identifier.urihttp://hdl.handle.net/10722/332290-
dc.description.abstractThe treble diastereoselectivities exhibited by Diels-Alder reactions which occur between diene and dienophilic components associated with bicyclic systems have been employed in the stepwise construction of compounds with molecular architectures that resemble cups and cages. These macropolycyclic compounds are potential synthetic precursors of novel hydrocarbons composed of [a,d]-fused and [a,c]-fused six-membered rings. The hydrocarbons themselves are of considerable importance in investigating the behaviour of π-electrons in highly-conjugated cyclic systems and in understanding the influence upon the aromaticity and antiaromaticity of benzenoid and fused benzenoid rings that are obliged to become bent. © 1993 IUPAC-
dc.languageeng-
dc.relation.ispartofPure and Applied Chemistry-
dc.titleThe structure-directed synthesis of cyclacene and polyacene derivatives-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1351/pac199365010119-
dc.identifier.scopuseid_2-s2.0-0001080623-
dc.identifier.volume65-
dc.identifier.issue1-
dc.identifier.spage119-
dc.identifier.epage125-
dc.identifier.eissn1365-3075-
dc.identifier.isiWOS:A1993KH16900016-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats