Add time:09/01/2019 Source:sciencedirect.com
Various S-substituted thiosuccinimides 1a-d and thiophthalimides 2a-d were found to react with trialkylphosphites according to a Michaelis-Arbuzov type mechanism. This provides an efficient way to prepare thiophosphoric acid (cas 13598-51-1) esters, particularly thiophospholipids, with a C-S-P bond.
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