RT info:eu-repo/semantics/article
T1 Synthesis of Pyrrolidine-Fused 1,3-Dithiolane Oligomers by the Cycloaddition of Polycyclic Dithiolethiones to Maleimides and Evaluation as Mercury(II) Indicators
A1 Fuertes Lázaro, Pedro
A1 García Valverde, María
A1 Cuevas Vicario, José Vicente
A1 Díaz de Greñu Puertas, Borja
A1 Rodríguez Rodríguez, Mª Teresa
A1 Rojo Cámara, Mª Josefa
A1 Torroba Pérez, Tomás
K1 Chemistry, Organic
K1 Química orgánica
AB The scandium triflate-catalyzed cycloaddition reactionof polycyclic 1,2-dithiolethiones to maleimides is described. Thereaction constitutes an easy approach to linear as well as branchedoligomeric cis-fused dihydro[1,3]dithiolo[4,5-c]pyrrole-4,6-dionerings interconnected by 3,5-diylidenethiomorpholine-2,6-dithione orylidene-6-thioxo[1,2]dithiolo[3,4-b][1,4]thiazin-3-one groups. Thepresence of highly colored, highly polarized push−pull α,β-unsaturated thione groups in their structures make these compoundssensitive to the presence of mercury(II) cation in organic or mixedorganic/aqueous solvents.
PB American Chemical Society
YR 2014
FD 2014-03
LK http://hdl.handle.net/10259/4360
UL http://hdl.handle.net/10259/4360
LA eng
NO Ministeriode Economíay Competitividad, Spain (Project CTQ2012-31611), Junta de Castilla y León, Consejeríade Educación yCultura y Fondo Social Europeo (Project BU246A12-1), and theEuropean Commission Seventh Framework Programme (ProjectSNIFFER FP7-SEC-2012-312411).
DS Repositorio Institucional de la Universidad de Burgos
RD 26-abr-2024