Russian Chemical Bulletin p. 2107 - 2109 (1997)
Update date:2022-08-10
Topics:
Kukharev
Stankevich
Klimenko
The reaction of oxazolidines with mercaptoacetic acid affords N-(2-hydroxyalkyl)-4-thiazolidinones in 58-87% yield regardless of the position of the oxazolidine - iminoalcohol tautomeric equilibrium. The structures of the resulting compounds were confirmed by IR and 1H NMR spectroscopy.
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