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Ligand‐Free Ullmann‐Type C–Heteroatom Couplings Under Practical Conditions
Author(s) -
Güell Imma,
Ribas Xavi
Publication year - 2014
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.201400033
Subject(s) - chemistry , iodobenzene , heteroatom , ligand (biochemistry) , bromobenzene , reactivity (psychology) , combinatorial chemistry , transmetalation , ullmann reaction , organic synthesis , coupling reaction , organic chemistry , solvent , dimethyl sulfoxide , catalysis , alternative medicine , pathology , medicine , ring (chemistry) , biochemistry , receptor
A new practical ligand‐free protocol for copper‐catalyzed C–heteroatom cross‐coupling reactions (Ullmann‐type) is described. The use of dimethyl sulfoxide (DMSO) as the solvent overcomes the need to use organic auxiliary ligands; thus, DMSO is revealed as a nontoxic and superior solvent for Ullmann‐type coupling reactions. This method allows the arylation of a wide range of amides, alcohols, and amines under practical conditions with bromobenzene and iodobenzene derivatives and will likely find direct application in current organic synthesis. The competitive reactivity among different functional groups is reported and rationalized, and the possibility to achieve selective arylation reactions is demonstrated.