Abstract
Alkynes add to (vinylketene)tricarbonyliron(0) complexes to generate stable adducts; addition of unsymmetrical alkynes is highly regioselective and the regiochemistries of the adducts produced in these reactions were determined by X-ray crystal structure analyses of the major isomer derived from but-3-yn-2-one and (3-tert-butyl-5-phenyl-1-oxapenta-1,2,4-triene)tricarbonyliron(0), and of the structurally modified product derived from diethylpropynylamine and (3-isopropyl-5-phenyl-1-oxapenta-1,2-4-triene)tricarbonyliron(0).
| Original language | English |
|---|---|
| Pages (from-to) | 1788-1791 |
| Number of pages | 4 |
| Journal | Journal of the Chemical Society, Chemical Communications |
| Issue number | 24 |
| Publication status | Published - 15 Dec 1992 |
Keywords
- CARBENE
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