THE REACTIVITY OF SULFUR NUCLEOPHILES TOWARDS ARENEDIAZONIUM TETRAFLUOROBORATES IN APROTIC SOLVENTS: SYNTHESIS OF S-ARYL THIOACETATES

DOI: 10.1016/S0040-4039(00)80451-7

Source and publish data:

Tetrahedron Letters p. 4185 - 4188 (1988)

Update date:2022-08-02

Topics:

Authors:

Petrillo, Giovanni

Novi, Marino

Garbarino, Giacomo

Filiberti, Marcos

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Article abstract of DOI:10.1016/S0040-4039(00)80451-7

Various S-aryl thioacetates are prepared in 40-60percent yield by treatment of arenediazonium tetrafluoroborates with commercial potassium thioacetate in DMSO at room temperature.

Full text of DOI:10.1016/S0040-4039(00)80451-7

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