Abstract
The bromoethynyl adduct of camphor was treated with equimolar amounts of iodine and Koser's reagent (HTIB) to afford in good yield and in good stereospecificity a (Z)-bromoiodoenone, a synthon for enantiospecific syntheses.
| Original language | English |
|---|---|
| Pages (from-to) | 4277-4280 |
| Number of pages | 4 |
| Journal | Tetrahedron Letters |
| Volume | 34 |
| Issue number | 27 |
| DOIs | |
| Publication status | Published - 2 Jul 1993 |
| Externally published | Yes |
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