Resumen
A cyclization of δ-(iodoacetoxy)-α,β-unsaturated ketones using iodotrimethylsilane involved a selective 1,4-addition of the acetate subunit to the enone and furnished δ-lactones in good yield.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 5567-5570 |
| Número de páginas | 4 |
| Publicación | Tetrahedron Letters |
| Volumen | 27 |
| N.º | 46 |
| DOI | |
| Estado | Published - 1986 |
Financiación
Acknowledgement. We thank the National Institutes of Health (GM 36256) for their generous support and Drs. K. Drauz and M. Bernd of Degussa AG, Hanau for a generous gift of chemicals.
| Financiadores | Número del financiador |
|---|---|
| National Institutes of Health (NIH) | GM 36256 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
Huella
Profundice en los temas de investigación de 'A δ-lactone synthesis involving an intramolecular 1,4-addition of α-iodoacetates to enones'. En conjunto forman una huella única.Citar esto
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