Please use this identifier to cite or link to this item: http://elar.urfu.ru/handle/10995/27091
Title: Efficient synthesis of novel thieno[3,2-b]-, [2,3-c]- and [3,2-c]pyridones by Sonogashira coupling of bromothiophenes with terminal alkynes and subsequent intramolecular C-N bond-forming reaction
Authors: Iaroshenko, V. O.
Ali, S.
Babar, T. M.
Abbasi, M. S. A.
Sosnovskikh, V. Y.
Villinger, A.
Tolmachev, A.
Langer, P.
Issue Date: 2013
Citation: Efficient synthesis of novel thieno[3,2-b]-, [2,3-c]- and [3,2-c]pyridones by Sonogashira coupling of bromothiophenes with terminal alkynes and subsequent intramolecular C-N bond-forming reaction / V. O. Iaroshenko, S. Ali, T. M. Babar [et al.] // Tetrahedron. — 2013. — Vol. 69. — № 15. — P. 3167-3181.
Abstract: The coupling of bromothiophenes with terminal alkynes using triethylamine or diisopropyl amine under Sonogashira conditions (PdCl2(PPh 3)2, CuI) followed by subsequent addition of amines or ammonium to the intermediate thienyl acetylenes represents a novel access to a wide range of thieno[3,2-b]-, [2,3-c]-, and [3,2-c]pyridones under basic conditions and in excellent yields. © 2013 Elsevier Ltd. All rights reserved.
Keywords: BROMOTHIOPHENES
SONOGASHIRA COUPLING
TERMINAL ALKYNES
THIENO[3,2-B]-, [2,3-C]-, AND [3,2-C]PYRIDONES
THIENYL ACETYLENES
ACETYLENE DERIVATIVE
ALKYNE DERIVATIVE
AMINE
AMMONIA
CARBON
NITROGEN
PYRIDONE DERIVATIVE
THIOPHENE DERIVATIVE
ADDITION REACTION
ARTICLE
CHEMICAL BOND
CHEMICAL STRUCTURE
CROSS COUPLING REACTION
CRYSTALLOGRAPHY
PRIORITY JOURNAL
SONOGASHIRA REACTION
SYNTHESIS
URI: http://elar.urfu.ru/handle/10995/27091
SCOPUS ID: 84875217651
WOS ID: 000316582400006
PURE ID: 922217
ISSN: 0040-4020
DOI: 10.1016/j.tet.2013.02.069
Appears in Collections:Научные публикации ученых УрФУ, проиндексированные в SCOPUS и WoS CC

Files in This Item:
File Description SizeFormat 
scopus-2013-0267.pdf600,5 kBAdobe PDFView/Open


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