Chemistry of Heterocyclic Compounds p. 951 - 953 (1987)
Update date:2022-08-04
Topics:
Bespalova, G. V.
Sedavkina, V. I.
Kharchenko, V. G.
Shebaldova, A. D.
Labunskaya, V. L.
It is shown that 1-substituted and N-substituted 5-R-pyrrolidine-2-thiones, in contrast to their oxygen analogs, undergo methylenethioalkylation and the Mannich and Michael reactions at the 3 position of the ring; this is due to their higher CH acidity.Th
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