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https://hdl.handle.net/2440/85944
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DC Field | Value | Language |
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dc.contributor.author | Warrener, R.N. | - |
dc.contributor.author | Evans, D.A.C. | - |
dc.contributor.author | Russell, R.A. | - |
dc.date.issued | 1984 | - |
dc.identifier.citation | Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1984; 25(42):4833-4836 | - |
dc.identifier.issn | 0040-4039 | - |
dc.identifier.issn | 1873-3581 | - |
dc.identifier.uri | http://hdl.handle.net/2440/85944 | - |
dc.description.abstract | Diels 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.statementofresponsibility | Ronald N. Warrener, David A.C. Evans, Richard A. Russell | - |
dc.language.iso | en | - |
dc.publisher | Pergamon Press | - |
dc.rights | © 1984 Pergamon Press Ltd. | - |
dc.source.uri | http://dx.doi.org/10.1016/s0040-4039(01)81532-x | - |
dc.title | Linear annelation of tricyclic quinones by site selective reaction with dienes | - |
dc.type | Journal article | - |
dc.identifier.doi | 10.1016/S0040-4039(01)81532-X | - |
pubs.publication-status | Published | - |
Appears in Collections: | Aurora harvest 2 Chemistry publications |
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