SYNTHESIS OF FUNCTIONALLY-SUBSTITUTED PYRROLOTHIAZOLIDINES FROM PYRROLE-2-CARBODITHIOATES, CH-ACIDS, AND HALOACETYLENES
Keywords:
haloacetylenes, CH-acids, pyrrole-2-carbodithioates, pyrrolothiazolidines, thiazines, halogenophilic attack, nucleophilic additionAbstract
Functionally substituted pyrrolothiazolidines have been synthesized by the sequential treatment of pyrrole-2-carbodithioates with methylene-reactive nitriles and haloacetylenes in a KOH–DMSO system.
How to Cite
Sobenina, L. N.; Demenev, A. P.; Mikhaleva, A. I.; Ushakov, I. A; Afonin, A. V.; D'yachkova, S. G.; Beskrylaya, E. A.; Oparina, L. A.; Elokhina, V. N.; Volkova, K. A.; Petrova, O. V.; Trofimov, B. A. Chem. Heterocycl. Compd. 2002, 38, 86. [Khim. Geterotsikl. Soedin. 2002, 95.]
For this article in the English edition, see DOI https://doi.org/10.1023/A:1014863511588