Please use this identifier to cite or link to this item:
Title: Suzuki-Miyaura cross-coupling reactions of aryl tellurides with potassium aryltrifluoroborate salts
Authors: Cella, R.
Cunha, RLOR
Reis, AES
Pimenta, D. C.
Klitzke, C. F.
Stefani, H. A.
Universidade de São Paulo (USP)
Universidade Federal de São Paulo (UNIFESP)
Inst Butantan
Issue Date: 6-Jan-2006
Publisher: Amer Chemical Soc
Citation: Journal of Organic Chemistry. Washington: Amer Chemical Soc, v. 71, n. 1, p. 244-250, 2006.
Abstract: Palladium(O)-catalyzed cross-coupling between potassium aryltrifluoroborate salts and aryl tellurides proceeds readily to afford the desired biaryls in good to excellent yield. the reaction seems to be unaffected by the presence of electron-withdrawing or electron-donating substituents in both the potassium aryltrifluoroborate salts and aryl tellurides partners. Biaryls containing a variety of functional groups can be prepared. A chemoselectivity study was also carried out using aryl tellurides bearing halogen atoms in the same compound. in addition, this new version of the Suzuki-Miyaura cross-coupling reaction was monitored by electrospray ionization mass spectrometry where some reaction intermediates were detected and analyzed.
ISSN: 0022-3263
Other Identifiers:
Appears in Collections:Em verificação - Geral

Files in This Item:
There are no files associated with this item.

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.