Ullmann-like reductive coupling of 1,4-diiodo-2,3,5,6-tetrafluorobenzene, promoted by copper(I) thiophene-2-carboxylate in N-methylpyrrolidinone at room temperature, followed by treatment with lithium aluminum hydride in THF, allowed us to obtain fluorinated poly(para-phenylene) oligomers containing up to five aromatic rings with hydrogen atoms as terminal groups. (C) 1998 Elsevier Science Ltd. All rights reserved.

A versatile copper-induced synthesis of fluorinated oligo(para-phenylenes)

BABUDRI, Francesco;FARINOLA, Gianluca Maria;
1998-01-01

Abstract

Ullmann-like reductive coupling of 1,4-diiodo-2,3,5,6-tetrafluorobenzene, promoted by copper(I) thiophene-2-carboxylate in N-methylpyrrolidinone at room temperature, followed by treatment with lithium aluminum hydride in THF, allowed us to obtain fluorinated poly(para-phenylene) oligomers containing up to five aromatic rings with hydrogen atoms as terminal groups. (C) 1998 Elsevier Science Ltd. All rights reserved.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/118059
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