TY - JOUR
T1 - Cross-coupling of aromatic esters and amides
AU - Takise, Ryosuke
AU - Muto, Kei
AU - Yamaguchi, Junichiro
N1 - Funding Information:
This work was supported by JSPS KAKENHI Grant No. JP16H01011, JP16H04148, JP16K13085, and 16H01140 (to J. Y.), JP16H07291 (to K. M.), and a JSPS research fellowship for young scientists (to T. S.). We thank Dr Yoshihiro Ishihara (Vertex Pharmaceuticals) for fruitful discussion and critical comments. This work is conducted as part of the Research Institute for Science and Engineering, Waseda University.
Publisher Copyright:
© 2017 The Royal Society of Chemistry.
PY - 2017/10/7
Y1 - 2017/10/7
N2 - Catalytic cross-coupling reactions of aromatic esters and amides have recently gained considerable attention from synthetic chemists as de novo and efficient synthetic methods to form C-C and C-heteroatom bonds. Esters and amides can be used as diversifiable groups in metal-catalyzed cross-coupling: in a decarbonylative manner, they can be utilized as leaving groups, whereas in a non-decarbonylative manner, they can form ketone derivatives. In this review, recent advances of this research topic are discussed.
AB - Catalytic cross-coupling reactions of aromatic esters and amides have recently gained considerable attention from synthetic chemists as de novo and efficient synthetic methods to form C-C and C-heteroatom bonds. Esters and amides can be used as diversifiable groups in metal-catalyzed cross-coupling: in a decarbonylative manner, they can be utilized as leaving groups, whereas in a non-decarbonylative manner, they can form ketone derivatives. In this review, recent advances of this research topic are discussed.
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U2 - 10.1039/c7cs00182g
DO - 10.1039/c7cs00182g
M3 - Review article
C2 - 28685781
AN - SCOPUS:85030625088
SN - 0306-0012
VL - 46
SP - 5864
EP - 5888
JO - Chemical Society Reviews
JF - Chemical Society Reviews
IS - 19
ER -