Adelaide Research & Scholarship
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https://hdl.handle.net/2440/85944
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| Type: | Journal article |
| Title: | Linear annelation of tricyclic quinones by site selective reaction with dienes |
| Author: | Warrener, R.N. Evans, D.A.C. Russell, R.A. |
| Citation: | Tetrahedron Letters: the international journal for the rapid publication of all preliminary communications in organic chemistry, 1984; 25(42):4833-4836 |
| Publisher: | Pergamon Press |
| Issue Date: | 1984 |
| ISSN: | 0040-4039 1873-3581 |
| Statement of Responsibility: | Ronald N. Warrener, David A.C. Evans, Richard A. Russell |
| 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. |
| Rights: | © 1984 Pergamon Press Ltd. |
| DOI: | 10.1016/S0040-4039(01)81532-X |
| Appears in Collections: | Aurora harvest 2 Chemistry publications |
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