SYNTHESIS OF <i>N</i>-ALKYLATED BENZO- AND PYRIDOTHIENOPYRROLO[1,2-<i>a</i>][1,4]DIAZEPIN-6-ONES ACTING AS ANTIDOTES AGAINST THE HERBICIDE 2,4-D
DOI:
https://doi.org/10.1007/2682Keywords:
annelated pyrrolo[1, 2-a][1, 4]diazepinones, N-alkylation, antidotes, biological activity, herbicide 2, 4-DAbstract
We report N-alkylation reactions of pyrrolo[1,2-a][1,4]diazepin-6-ones annelated with a benzene ring or thieno[2,3-b]pyridine system. A range of new N5-substituted pyrrolodiazepines were synthesized, including compounds acting as antidotes against the herbicide 2,4-D.
How to Cite
Stroganova, T. A.; Vasilin, V. K.; Krapivin, G. D.; Strelkov, V. D.; Dyadyuchenko, L. V. Chem. Heterocycl. Compd. 2016, 52, 45. [Khim. Geterotsikl. Soedin. 2016, 52, 45.]
For this article in the English edition see DOI 10.1007/s10593-016-1830-x