A novel formation of thiocarbonyl compounds from phosphorus ylides with cyclic polysulfide as the sulfuration reagent

DOI: 10.1055/s-1991-26574

Source and publish data:

Synthesis p. 785 - 786 (1991)

Update date:2022-08-02

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Authors:

Sato Sato

Satoh Satoh

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Article abstract of DOI:10.1055/s-1991-26574

The reaction of cyclic polysulfides, such as 5H-1,2,3,4-benzotetrathiepin and 6H-1,2,3,4,5-benzopentathiocin as the sulfuration reagent with relatively stable phosphorus ylides affords efficiently thiocarbonyl compounds such as thioaldehydes and thioketon

Full text of DOI:10.1055/s-1991-26574

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