1-Acyloxy-2(1H)-pyrimidine-2-thiones as novel radical precursors

DOI: 10.1016/0040-4039(94)88211-8

Source and publish data:

Tetrahedron Letters p. 7009 - 7012 (1994)

Update date:2022-08-02

Topics:

Authors:

Liebscher, Juergen

Riemer, Beate

Bendig, Juergen

Stoesser, Reinhard

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Article abstract of DOI:10.1016/0040-4039(94)88211-8

Reaction of 3-isothiocyanato-2-propeniminium perchlorates 1 with hydroxylamine gives 1-hydroxy-2(1H)-pyrimidine-2-thiones 2 which can be O-acylated. The resulting 1-acyloxy-2(1H)-pyrimidine-2-thiones 4 are novel precursors for organic radicals. Their photochemical homolysis is studied and affords disulfides 5, 2-alkylthiopyrimidines 6 and alkanes 7 and 8.

Full text of DOI:10.1016/0040-4039(94)88211-8

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