162878-69-5Relevant articles and documents
Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki-Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides
Botteselle, Giancarlo V.,Hough, Thomas L. S.,Venturoso, Raphael C.,Cella, Rodrigo,Vieira, Adriano S.,Stefani, Helio A.
, p. 870 - 873 (2008)
The Suzuki-Miyaura cross-coupling reaction of 2-(butyltellanyl) or 2,5-bis-(butyltellanyl)furans and thiophenes with potassium aryltrifluoroborate salts catalyzed by palladium afforded 2-aryl- or 2,5-diaryl-furans and thiophenes in moderate to good yields.
Models for intramolecular exchange in organic π-conjugated open-shell systems: 3-Nitrenophenyl and 4-nitrenophenyl units connected by 2,5-furandiyl, 2,5-thiophenediyl, and 2,5-pyrrolediyl nonalternant exchange linkers
Ling, Chris,Lahti, Paul M.
, p. 8784 - 8792 (2007/10/02)
The first bis(arylnitrenes) linked by heterocyclic pseudoaromatic rings were generated in a glassy, 77 K 2-methyltetrahydrofuran matrix by photolysis at wavelengths >300 nm: 2,5-bis(3-nitrenophenyl)furan (1); 2,5-bis-(3-nitrenophenyl)thiophene (2); 2,5-bi