The document discusses the thermal cycloreversion of 4H-1,3-dioxine-4-thiones to acyl thioketenes. This reaction generates reactive intermediates that can be trapped with nucleophiles to form β-ketothioic O-acid derivatives and related products.
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Sato 2010
The document discusses the thermal cycloreversion of 4H-1,3-dioxine-4-thiones to acyl thioketenes. This reaction generates reactive intermediates that can be trapped with nucleophiles to form β-ketothioic O-acid derivatives and related products.
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1996 thio compounds
thio compounds (acyclic compounds)
P 0440 Thermal Cycloreversion of 4H-1,3-Dioxine-4-thiones to Acyl 36 - 072 Thioketenes: A General Synthesis of β-Ketothioic O-Acid Deriva- tives. — Thermal cycloreversion of the title thiones such as (I) gives acyl thioketenes as reactive intermediates. Trapping of these intermediates with nucleophiles leads to β-ketothioic O-acid derivatives such as (III) or (VI) and some related products. — (SATO, M.; BAN, H.; UEHARA, F.; KANEKO, C.; Chem. Commun. (Cambridge) (1996) 6, 775-776; Pharm. Inst., Tohoku Univ., Sendai 980-77, Japan; EN)