Tetraformyltetrathiafulvalene (TFTTF) and acetals, precursors of polyfunctionalized TTFs.
摘要:
A short synthesis of 1,3-dithiol-2-thiones bearing two aldehyde functionalities, free and/or masked as diethylacetals is described. They are shown to be convenient precursors for synthesizing di- and tetraformyl-TTF. When submitted to four-fold nucleophilic attacks, the latter readily affords new substituted derivatives such as the bis-(pyridazino)-TTF 8, the tetrakis-(hydroxymethyl)-TTF 9 and the tetravinylic-TTF 10 whose pi-donor ability has been characterized.
A short synthesis of 1,3-dithiol-2-thiones bearing two aldehyde functionalities, free and/or masked as diethylacetals is described. They are shown to be convenient precursors for synthesizing di- and tetraformyl-TTF. When submitted to four-fold nucleophilic attacks, the latter readily affords new substituted derivatives such as the bis-(pyridazino)-TTF 8, the tetrakis-(hydroxymethyl)-TTF 9 and the tetravinylic-TTF 10 whose pi-donor ability has been characterized.
Salle, Marc; Gorgues, Alain; Jubault, Michel, Bulletin de la Societe Chimique de France, 1996, vol. 133, # 4, p. 417 - 426
作者:Salle, Marc、Gorgues, Alain、Jubault, Michel、Boubekeur, Kamal、Batail, Patrick、Carlier, Roger