In a recent publication (1) we have reported the light-induced addition of acetals to olefins which led to the corresponding monoalkyl acetal derivatives. We report now the peroxide-induced addition of 1.3,5-trioxan to olefins at elevated temperatures.
Free-radical addition to olefins of an H2S equivalent: Triphenylsilanethiol
✍ Scribed by Bruno Haché; Yves Gareau
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- French
- Weight
- 210 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
The tr&benyLsnytbiyl dical gcperated dmnally (AIBN-I or pbmdmnicalty in tbe pmsemce ofan olefin yields tbe anti-Vv H$ addua after-by aitltwmacek add (TFA).
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Polymer bound olefins undergo free radical initiated 1,2-addition when reacted with a variety of haloalkanes. The strategy could be applied successfully to the solid-phase synthesis of dihaloethenylcyclopropane carboxylic acids which are the key fragments of synthetic pyrethroids.