TY - JOUR
T1 - Recent progress of transition metal-catalysed regioselective C-H transformations based on noncovalent interactions
AU - Kuninobu, Yoichiro
AU - Torigoe, Takeru
N1 - Funding Information:
This work was supported in part by JSPS KAKENHI Grant Numbers JP 17H03016 and 18H04656 and Yamada Science Foundation.
Publisher Copyright:
© The Royal Society of Chemistry 2020.
PY - 2020/6/14
Y1 - 2020/6/14
N2 - Transition metal-catalysed C-H transformations are powerful methods to obtain functionalised organic molecules from simple starting materials. Controlling regioselectivity is one of the most important issues in C-H transformations. Since the remarkable work by Murai and co-workers in 1993, many groups have reportedortho-selective C(sp2)-H transformations using directing group methods, in which interactions exist between substrates and catalytically active metal centres. In this review, new methodologies to achieve regioselective C-H transformations are described. In these methhodologies, noncovalent interactions between substrates and reagents or ligands of catalysts play important roles. In these cases, selective functionalization of remote C-H bonds, such asmeta- andpara-C-H bonds, can also be realized.
AB - Transition metal-catalysed C-H transformations are powerful methods to obtain functionalised organic molecules from simple starting materials. Controlling regioselectivity is one of the most important issues in C-H transformations. Since the remarkable work by Murai and co-workers in 1993, many groups have reportedortho-selective C(sp2)-H transformations using directing group methods, in which interactions exist between substrates and catalytically active metal centres. In this review, new methodologies to achieve regioselective C-H transformations are described. In these methhodologies, noncovalent interactions between substrates and reagents or ligands of catalysts play important roles. In these cases, selective functionalization of remote C-H bonds, such asmeta- andpara-C-H bonds, can also be realized.
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U2 - 10.1039/d0ob00703j
DO - 10.1039/d0ob00703j
M3 - Review article
C2 - 32432310
AN - SCOPUS:85086337267
SN - 1477-0520
VL - 18
SP - 4126
EP - 4134
JO - Organic and Biomolecular Chemistry
JF - Organic and Biomolecular Chemistry
IS - 22
ER -