27.4.3 Thioaldehyde and Thioketone S-Oxides and S-Imides (Sulfines and Derivatives) (Update 2014)
计算机科学
作者
G. Mlostoń,H. Heimgartner
出处
期刊:Haug Verlag in Georg Thieme Verlag KG eBooks [Georg Thieme Verlag] 日期:2014-01-01
标识
DOI:10.1055/sos-sd-127-00361
摘要
Abstract This chapter is an update to the earlier Science of Synthesis contribution describing methods of synthesis and new applications for thiocarbonyl S-oxides (sulfines) and thiocarbonyl S-imides. In general, thiocarbonyl S-oxides are more stable and in many instances can be isolated. The in situ generated thiocarbonyl S-imides are efficient “sulfur-transfer agents” via the isomeric thiaziridines, formed as products of electrocyclic ring closure. Stable thiocarbonyl S-imides, derived from hexafluorothioacetone, are useful 1,3-dipoles and are applied in the preparation of fluorinated five-membered heterocycles.