TY - JOUR
T1 - Toward an ideal synthesis of (Bio)molecules through direct arene assembling reactions
AU - Yamaguchi, Junichiro
AU - Itami, Kenichiro
N1 - Funding Information:
This work was supported by the Funding Program for Next Generation World-Leading Researchers from JSPS (220GR049 to K.I.), KAKENHI (21675002 to K.I.; 22750037, 23105517, 25105720, 25708005, 16H01011, 16H04148, and 16H01140 to J.Y.) from MEXT, Uehara Foundation (to J.Y.), Naito Foundation (to J.Y.), and Sumitomo Foundation (to J.Y.). ITbM is supported by the World Premier International Research Center (WPI) Initiative, Japan.
Publisher Copyright:
© 2017 The Chemical Society of Japan.
PY - 2017
Y1 - 2017
N2 - CH (hetero)arylation of aromatic compounds using transition-metal catalysts has garnered much attention from the synthetic chemistry community as a next-generation coupling method for constructing (hetero)biaryl motifs. This account describes our recent achievements in transitionmetal- catalyzed aromatic CH arylation and its applications to the synthesis of bioactive molecules.
AB - CH (hetero)arylation of aromatic compounds using transition-metal catalysts has garnered much attention from the synthetic chemistry community as a next-generation coupling method for constructing (hetero)biaryl motifs. This account describes our recent achievements in transitionmetal- catalyzed aromatic CH arylation and its applications to the synthesis of bioactive molecules.
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U2 - 10.1246/bcsj.20160365
DO - 10.1246/bcsj.20160365
M3 - Article
AN - SCOPUS:85020449106
SN - 0009-2673
VL - 90
SP - 367
EP - 383
JO - Bulletin of the Chemical Society of Japan
JF - Bulletin of the Chemical Society of Japan
IS - 4
ER -