147915-94-4Relevant articles and documents
Synthesis and redox properties of pyrroledithiocarboxylic acid esters
Sobenina, L. N.,Protasova, L. E.,Sergeeva, M. P.,Petrova, O. V.,Aksamentova, T. N.,et al.
, p. 40 - 46 (1995)
Pyrrole-2-dithiocarboxylates were obtained by reacting alkylpyrroles with carbon disulfide in the presence of alkyl halides in the KOH-DMSO system.The pyrrole and its aryl derivatives were primarily converted into pyrrole-1-dithiocarboxylates in these conditions.The electronic structure and redox properties of the synthesized compounds were investigated by polarography and cyclic voltammtry.
Synthesis of functionalized 2,2′- and 2,3′-bipyrroles via 3-imino-3H-pyrrolizine-2-carbonitriles
Petrova, Olga V.,Sagitova, Elena F.,Sobenina, Lyubov N.,Ushakov, Igor A.,Borodina, Tat′yana N.,Smirnov, Vladimir I.,Trofimov, Boris A.
, p. 3652 - 3656 (2016/07/21)
A novel strategy for the synthesis of 4-amino-3-cyano-2,2′- and 5′-amino-4′-cyano-2,3′-bipyrroles via readily available 1-amino-3-imino-3H-pyrrolizine-2-carbonitriles has been developed. The rearrangement leading to 5′-amino-4′-cyano-2,3′-bipyrroles involves formation of the intermediate aziridine, which undergoes other side ring-opening.
REACTION OF PYRROLES WITH CARBON DISULFIDE IN KOH/DMSO SYSTEM
Trofimov, B. A.,Sobenina, L. N.,Mikhaleva, A. I.,Sergeeva, M. P.,Golovanova, N. I.,et al.
, p. 990 - 994 (2007/10/02)
By the interaction of pyrroles with carbon disulfide and haloalkanes in a KOH/DMSO system, esters of 1- and 2-pyrrolyldithiocarboxylic acids have been synthesized.The influence of substituents on the direction of the reaction has been established.
