Sulfation made simple: A strategy for synthesising sulfated molecules

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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.

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Gill, D. M., Male, L., & Jones, A. M. (2019). Sulfation made simple: A strategy for synthesising sulfated molecules. Chemical Communications, 55(30), 4319–4322. https://doi.org/10.1039/c9cc01057b

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