Abstract
The study of organosulfates is a burgeoning area in biology, yet there are significant challenges with their synthesis. We report the development of a tributylsulfoammonium betaine as a high yielding route to organosulfates. The optimised reaction conditions were interrogated with a diverse range of alcohols, including natural products and amino acids.
Original language | English |
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Pages (from-to) | 4319-4322 |
Number of pages | 4 |
Journal | Chemical Communications |
Volume | 55 |
Issue number | 30 |
Early online date | 12 Mar 2019 |
DOIs | |
Publication status | Published - 12 Mar 2019 |
ASJC Scopus subject areas
- Catalysis
- Electronic, Optical and Magnetic Materials
- Ceramics and Composites
- General Chemistry
- Surfaces, Coatings and Films
- Metals and Alloys
- Materials Chemistry