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- W2022668598 abstract "Oxa(thia)diazole adducts 2a-d, DMSO and azole Schiff bases la-d are chemoselectively annulated with sulfuric acid, acetic acid, and thionyl chloride to yield imidazo[2,1-b]-1,3,4-oxa(thia)diazoles 3a-d. Their 5-methylsulfenyl analogues 4a-d and 1,3,4-oxa(thia)diazolo[3,2-b]-1,2,4-thiadiazines 5a-d, respectively, 3-5 are formed via demethylsulfinylation, the Pummerer rearrangement, and deoxygenative demethylation, in a one-pot procedure." @default.
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- W2022668598 date "2003-10-14" @default.
- W2022668598 modified "2023-09-27" @default.
- W2022668598 title "Novel Chemoselective Annulation of Imidazole and 1,2,4-Thiadiazine Rings on Azoles Involving Acid Labile Methanesulfinyl Group" @default.
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- W2022668598 doi "https://doi.org/10.1002/chin.200341163" @default.
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