A new synthesis of thiophosphoric acid esters with a C-S-P bond

DOI: 10.1016/0040-4039(90)87018-U

Source and publish data:

Tetrahedron Letters p. 501 - 502 (1990)

Update date:2022-08-03

Topics:

Authors:

Muller Muller

Roth Roth

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Article abstract of DOI:10.1016/0040-4039(90)87018-U

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 esters, particularly thiophospholipids, with a C-S-P bond.

Full text of DOI:10.1016/0040-4039(90)87018-U

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