Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/85944
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dc.contributor.authorWarrener, R.N.-
dc.contributor.authorEvans, D.A.C.-
dc.contributor.authorRussell, R.A.-
dc.date.issued1984-
dc.identifier.citationTetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1984; 25(42):4833-4836-
dc.identifier.issn0040-4039-
dc.identifier.issn1873-3581-
dc.identifier.urihttp://hdl.handle.net/2440/85944-
dc.description.abstractDiels Alder reactions involving tricyclic quinones of type (3) proceed at the internal pi-bond unless the terminal pi-bond is substituted with an activating substituent, e.g. So2Ar. Thermal isomerisation of the internal adducts leads to the formation of linear but aromatised products some of which can be made to retain their bridge.-
dc.description.statementofresponsibilityRonald N. Warrener, David A.C. Evans, Richard A. Russell-
dc.language.isoen-
dc.publisherPergamon Press-
dc.rights© 1984 Pergamon Press Ltd.-
dc.source.urihttp://dx.doi.org/10.1016/s0040-4039(01)81532-x-
dc.titleLinear annelation of tricyclic quinones by site selective reaction with dienes-
dc.typeJournal article-
dc.identifier.doi10.1016/S0040-4039(01)81532-X-
pubs.publication-statusPublished-
Appears in Collections:Aurora harvest 2
Chemistry publications

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