Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 5567-5570 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 27 |
| Issue number | 46 |
| DOIs | |
| State | Published - 1986 |
Funding
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.
| Funders | Funder number |
|---|---|
| National Institutes of Health (NIH) | GM 36256 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry
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