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| | Transition Metal Catalysed 1-Oxa-1,3-diene Formation (Site not responding. Last check: 2007-11-02) |
 | | At 80°C, where all the metal catalysed reactions were performed, the thermal dehydration is hardly proceeding at all (4% conversion, entry 2) and can thus be neglected as competing reaction. |
 | | As obvious from the iodine catalysed dehydration reaction (entry 5, Table 1a) proceeding under thermodynamic control, the conjugated and non-conjugated enones 2 and 3 are of very similar stability. |
 | | As a mechanistic explanation for the observed dehydration regioselectivity, formation of hydroxo-metal intermediates and subsequent abstraction of a proton from the sterically less hindered, i.e. |
| www.ch.ic.ac.uk /ectoc/papers/07 (2969 words) |
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