Synthesis and redox properties of pyrroledithiocarboxylic acid esters

Autor:	M. P. Sergeeva, Lubov N. Sobenina, A. I. Mikhaleva, Tamara N. Aksamentova, Boris A. Trofimov, O. B. Kozyreva, Olga V. Petrova, L. E. Protasova, R. I. Polovnikova
Rok vydání:	1995
Předmět:	chemistry.chemical_classification chemistry.chemical_compound Polarography Carbon disulfide chemistry Aryl Organic Chemistry Polymer chemistry Halide Cyclic voltammetry Redox Alkyl Pyrrole
Zdroj:	Chemistry of Heterocyclic Compounds. 31:40-46
ISSN:	1573-8353 0009-3122
DOI:	10.1007/bf01171288
Popis:	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 voltammetry.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::f931b8c23fb7073df4b0eb90e30405a8 https://doi.org/10.1007/bf01171288 Zobrazit plný text záznamu Full text from SpringerLink