Carbon-Carbon Bond Formation via Intramolecular Cycloadditions: Use of the Thiocarbonyl Ylide Dipole in anhydro-4-Hydroxythiazolium Hydroxides
The mesoionic systems resulting from the introduction of 2-(allyloxy)phenyl substituents into the 2-, 3-, and 5-positions of anhydro-4-hydroxythiazolium hydroxide undergo intramolecular cycloaddition under different reaction conditions, the ease of cycloa
Potts, Kevin T.,Dery, Maurice O.,Juzukonis, Walter A.
anhydro-2-(2-Allyloxyphenyl)-3,5-diphenyl-4-hydroxy-6-oxo-1,3-thiazinium hydroxide and the corresponding ethynyl derivative underwent ready thermal 1,4-dipolar cycloaddition to give a 1:1-cycloadduct (whose structure was determined by X-ray crystallograph
Potts, Kevin T.,Dery, Maurice O.
p. 563 - 565
(2007/10/02)
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