• 약학회지
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• 제59권2호
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• pp.66-69
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• 2015

A concise synthesis of flurbiprofen, a member of the non-steroidal anti-inflammatory 2-arylpropionic acids, has been accomplished. The key feature of this synthesis involves successive palladium-catalyzed cross coupling reactions. In particular, a 2-arylacylate intermediate, which easily converted to the key 2-arylpropionic acid scaffold, was afforded by a versatile palladium-catalyzed cross coupling reaction between diazopropanate and bisphenylboronic acid. This synthetic procedure would facilitate synthesis of the flurbiprofen and anti-inflammatory 2-arylpropionic acid derivatives.

• Bulletin of the Korean Chemical Society
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• 제34권3호
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• pp.983-985
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• 2013

• Bulletin of the Korean Chemical Society
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• 제32권spc8호
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• pp.2970-2972
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• 2011

One-pot homo- and cross-coupling reactions of arenediazonium tosylate salts bearing a halogen group have been exploited for the synthesis of biaryls and polyaryls under mild conditions. $Pd(OAc)_2$ has proven to be an efficient catalyst for the successful dual transformation of diazonium salts into p-quaterphenyl (3).

• Bulletin of the Korean Chemical Society
• /
• 제35권1호
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• pp.280-282
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• 2014

• Bulletin of the Korean Chemical Society
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• 제23권12호
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• pp.1823-1826
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• 2002

• Bulletin of the Korean Chemical Society
• /
• 제32권1호
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• pp.359-362
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• 2011

• Bulletin of the Korean Chemical Society
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• 제28권11호
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• pp.1929-1930
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• 2007

• Bulletin of the Korean Chemical Society
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• 제34권5호
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• pp.1477-1480
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• 2013

The Suzuki cross-coupling reactions proceeded in excellent yields when it was catalyzed by magnetically recyclable nanocatalyst. This nanocatalyst provided very high catalytic activity with low loading level (1 mol %), because the palladium nanoparticles were so small in size (~2 nm) and located on the surface of the nanocomposite. It was also easily recovered from the reaction mixture using a magnet and reused for six consecutive cycles.

• Bulletin of the Korean Chemical Society
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• 제30권3호
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• pp.726-728
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• 2009

• Bulletin of the Korean Chemical Society
• /
• 제24권11호
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• pp.1632-1636
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• 2003

Palladium-catalyzed cross-coupling reactions of neopentyloxysulfonylphenyl bromides with arylboronic acids provided a variety of neopentyl biphenylsulfonates in good yields. 2-Bromo- and 4-bromobenzenesulfonates underwent the coupling reaction more rapidly than 3-bromobenzenesulfonate, while chlorobenzenesulfonate did not produce the coupling product under the standard reaction conditions.