Se-Phenyl p-tolueneselenosulfonate (1) undergoes thermal addition to acetylenes to afford P-(phenylseleno)vinyl sulfone adducts 2 in a stereo-and regioselective fashion. -We recently reported that Se-phenyl areneselenosulfonates (e.g. 1) add to olefins on heating or at room temperature in the presen
Selenosulfonation of acetylenes. Substitution reactions of β-(phenylseleno)vinyl sulfones with organocuprates
✍ Scribed by Thomas G. Back; Scott Collins; Kwok-Wai Law
- Publisher
- Elsevier Science
- Year
- 1984
- Tongue
- French
- Weight
- 212 KB
- Volume
- 25
- Category
- Article
- ISSN
- 0040-4039
No coin nor oath required. For personal study only.
✦ Synopsis
P-(Phenylseleno)vinyl sulfones are readily available from the selenosulfonation of acetylenes and undergo efficient, stereoselective substitution of the phenylseleno moiety by the alkyl group of alkyl (phenylseleno)cuprates.
📜 SIMILAR VOLUMES
## Reaction of Mo( NO),( CHMe) (OR),( AlCl\*) ( EtAlCI,) (R = Et, 0-i-Pr) with vinyl silanes (vinyltrimethoxysilane and vinyltrimethylsilane) with substituted acetylenes (phenylacetylene and hex-2-yne) are studied. The ethylidene complex has been found to be an efficient catalyst for metathesis r
In the previous paper, 1) we described that S-vinyl sulfilimines(l\_) react with protic nucleophiles(HNu) such as alcohols, thiols, secondary aromatic amines and active methylenes to give Michael type adducts(2).