Selective sulfonylation of 1,2-diols and derivatives catalyzed by a recoverable fluorous tin oxide
✍ Scribed by Brian Bucher; Dennis P Curran
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- French
- Weight
- 72 KB
- Volume
- 41
- Category
- Article
- ISSN
- 0040-4039
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✦ Synopsis
Fluorous tin oxide (C 6 F 13 CH 2 CH 2 ) 2 SnO is readily synthesized, exhibits spectra that are generally similar to dibutyltin oxide and appears to exist as an oligomer or polymer. The fluorous tin oxide can be used catalytically to effect the selective monotosylation of 1,2-diols with TsCl/Et 3 N, and it can be readily recovered and reused.
📜 SIMILAR VOLUMES
## Abstract We present a general, practical, and efficient approach to 5‐ and 6‐membered organic carbonates by palladium‐catalyzed direct oxidative carbonylation of 1,2‐ and 1,3‐diols, respectively. Reactions were carried out at 100 °C in __N__,__N__‐dimethylacetamide as the solvent under 20 atm (a