Department of Chemistry, Graduate School of Science, Kyoto University, Kyoto 606-8502, Japan.
Chemistry. 2013 May 27;19(22):7156-61. doi: 10.1002/chem.201300623. Epub 2013 Apr 4.
Triisopropylsilyltetrathiafulvalene (TIPS-TTF) has been devised as a promising platform for the synthesis of low-symmetry TTF derivatives. The bulky TIPS group allows TIPS-TTF to undergo palladium-catalyzed direct diarylation as well as LDA-mediated dilithiation exclusively on the roomier dithiole ring. Subsequent fluoride-mediated protodesilylation provided vicinally difunctionalized TTF, which could undergo further functionalization.
三异丙基硅基四硫富瓦烯(TIPS-TTF)已被设计为合成低对称 TTF 衍生物的有前途的平台。庞大的 TIPS 基团允许 TIPS-TTF 经历钯催化的直接二芳基化以及 LDA 介导的二锂化,仅在更宽敞的二噻咯环上进行。随后的氟化物介导的脱硅基化提供了邻位二官能化的 TTF,可以进一步进行官能化。