Title of article :
Synthesis of tetraaryl-p-benzoquinones and 2,3-diaryl-1,4-naphthoquinones via Suzuki–Miyaura cross-coupling reactions
Author/Authors :
Zahid Hassan، نويسنده , , Ihsan Ullah، نويسنده , , Iftikhar Ali Shah، نويسنده , , Rasheed Ahmad Khera، نويسنده , , Ingo Knepper، نويسنده , , Asad Ali، نويسنده , , Tam?s Patonay، نويسنده , , Alexander Villinger، نويسنده , , Peter Langer، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
10
From page :
460
To page :
469
Abstract :
The palladium-catalyzed Suzuki–Miyaura coupling reaction of tetrabromo-p-benzoquinone and 2,3-dibromonaphthoquinone provide a convenient approach to tetraaryl-p-benzoquinones and 2,3-diarylnaphthoquinones. Suzuki–Miyaura of tetrabromo-1,4-phenylene bis(trifluoromethanesulfonate) and of 2,3-dibromonaphthalene-1,4-diyl bis(trifluoromethanesulfonate) resulted in the formation of the same type of quinone products instead of the expected benzene and naphthalene derivatives.
Keywords :
Palladium , Suzuki–Miyaura reaction , Naphthalene , Catalysis , Benzoquinone
Journal title :
Tetrahedron
Serial Year :
2013
Journal title :
Tetrahedron
Record number :
1105325
Link To Document :
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