A novel reagent for the synthesis of geminal di-sulfones
β Scribed by Michael J Hadd; Mark A Smith; Jacquelyn Gervay-Hague
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- French
- Weight
- 107 KB
- Volume
- 42
- Category
- Article
- ISSN
- 0040-4039
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β¦ Synopsis
A novel reagent (diisopropoxyphosphorylmethanesulfonylmethanesulfonylmethyl)-phosphonic acid diisopropyl ester (8) capable of forming symmetrical and non-symmetrical a,b unsaturated gem-disulfones is reported. Both aromatic and aliphatic aldehydes react in good yields to give exclusively the trans isomer. Selectivity for the mono-olefin can be achieved by varying the stoichiometry of reagents.
π SIMILAR VOLUMES
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Two novel polystyrene-supported selenosulfonate reagents have been developed for AIBN-catalyzed addition to acetylenes and have been used for the synthesis of acetylenic sulfones.