143541-34-8Relevant articles and documents
Transition-Metal-Free Synthesis of Trifluoromethylated Furans via a Bu3P-Mediated Tandem Acylation-Wittig Reaction
Li, Maizhan,Zhou, Wei
, p. 2035 - 2038 (2020)
A highly efficient nucleophilic addition- O -acylation-intramolecular Wittig reaction of β-trifluoromethyl α,β-enones is disclosed. This strategy features mild reaction conditions and provides a practical transition-metal-free method to a set of biologically significant trifluoromethylated furans in high yields with diverse functional groups.
Ein neues Verfahren zur positionsselektiven Einfuehrung von Trifluormethylgruppen in Heteroaromaten: Synthese von 3-Trifluormethylfuranen
Burger, Klaus,Helmreich, Brigitte
, p. 311 - 316 (2007/10/02)
Transformation of 4,4-bis(trifluoromethyl)-1-oxabuta-1,3-dienes (2) into 2-fluoro-3-trifluoromethylfurans (4) can be achieved in a two step procedure by treatment with tin(II) chloride and sodium hydride.The fluorine atom at skeleton position 2 is replace