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.

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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Synthesis of 2-Aryl- and 2,5-Diarylfurans and Thiophenes by Suzuki-Miyaura Reactions Using Potassium Trifluoroborate Salts and Heteroaryltellurides

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Author(s):	Botteselle, Giancarlo V. ^[1] ; Hough, Thomas L. S. ^[1] ; Venturoso, Raphael C. ^[1] ; Cella, Rodrigo ^[2] ; Vieira, Adriano S. ^[1] ; Stefani, Helio A. ^{[2, 1, 3]} Total Authors: 6
Affiliation:	^[1] Univ Sao Paulo, Fac Ciencias Farmaceut, Sao Paulo - Brazil ^[2] Univ Sao Paulo, Inst Quim, Sao Paulo - Brazil ^[3] Univ Fed Sao Paulo, Deparmento Biofis, Sao Paulo - Brazil Total Affiliations: 3
Document type:	Journal article
Source:	AUSTRALIAN JOURNAL OF CHEMISTRY; v. 61, n. 11, p. 870-873, 2008.
Web of Science Citations:	12
Abstract
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. (AU)

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