Title of article :
Chemoselective Suzuki–Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate
Author/Authors :
Khaddour، نويسنده , , Zien and Eleya، نويسنده , , Nadi and Akrawi، نويسنده , , Omer A. and Hamdy، نويسنده , , Aws M. and Patonay، نويسنده , , Tamلs and Villinger، نويسنده , , Alexander and Langer، نويسنده , , Peter، نويسنده ,
Issue Information :
هفته نامه با شماره پیاپی سال 2013
Pages :
3
From page :
5201
To page :
5203
Abstract :
Arylated naphthalenes were prepared by Suzuki–Miyaura cross-coupling reactions of methyl 4-bromo-3-(trifluoromethylsulfonyloxy)-2-naphthoate. The reactions proceeded with very good chemoselectivity in favor of the triflate group, due to additive electronic ortho electronic effects.
Keywords :
naphthalene , PALLADIUM , Suzuki–Miyaura reaction , Chemoselectivity , Catalysis
Journal title :
Tetrahedron Letters
Serial Year :
2013
Journal title :
Tetrahedron Letters
Record number :
1885549
Link To Document :
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