Publication | Closed Access
Synthesis and reactions of 3‐iodo‐4<i>H</i>‐pyran‐4‐ones
16
Citations
11
References
1986
Year
H ‐Pyran‐4‐onesHeterocyclicOrganic ChemistrySynthetic ChemistryStereoselective SynthesisChemistryHeterocycle ChemistryPharmacologyIodine MonochlorideEnantioselective SynthesisH ‐Pyran‐4‐thiones
Abstract 3‐Iodo‐4 H ‐pyran‐4‐ones have been synthesised in excellent yield by the reaction of acetylenic β‐diketones with iodine monochloride and were converted into the corresponding 4 H ‐pyran‐4‐thiones. The iodopyrones and thiopyrones gave with methylamine the respective N ‐methylpyridones and thiopyridones. The structure of the above compounds was confirmed from their spectral characteristics.
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