Issue 30, 2019

Sulfation made simple: a strategy for synthesising sulfated molecules

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.

Graphical abstract: Sulfation made simple: a strategy for synthesising sulfated molecules

Supplementary files

Article information

Article type
Communication
Submitted
05 Feb 2019
Accepted
12 Mar 2019
First published
12 Mar 2019
This article is Open Access
Creative Commons BY license

Chem. Commun., 2019,55, 4319-4322

Sulfation made simple: a strategy for synthesising sulfated molecules

D. M. Gill, L. Male and A. M. Jones, Chem. Commun., 2019, 55, 4319 DOI: 10.1039/C9CC01057B

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