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Rhodium-Catalysed Enantioselective C-H Functionalization in Asymmetric Synthesis
被引:44
|作者:
Motevalli, Somayeh
[1
]
Sokeirik, Yasser
[1
]
Ghanem, Ashraf
[1
]
机构:
[1] Univ Canberra, Fac ESTEM, Dept Biomed Sci, ACT, Kirinari St, Bruce 2601, Australia
关键词:
Asymmetric catalysis;
Enantioselectivity;
Homogeneous catalysis;
Rhodium;
C-C coupling;
C-H activation;
Chiral ligands;
P ligands;
CARBON-HYDROGEN BONDS;
CHIRAL CYCLOPENTADIENYL LIGANDS;
CROSS-COUPLING REACTIONS;
BRANCHED ALLYLIC ESTERS;
TERMINAL ALKYNES;
DIRECT ARYLATION;
REVERSE PRENYLATION;
AROMATIC KETIMINES;
ORTHO-ALKENYLATION;
ORGANIC-SYNTHESIS;
D O I:
10.1002/ejoc.201501425
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
In this review, recent advances in the utilization of two classes of rhodium catalysts - namely rhodium(I) and rhodium(III) - in complexation with chiral cyclopentadienyl and phosphorus ligands in inter-and intramolecular asymmetric C-H bond activation/functionalization of aromatic and vinylic compounds is discussed. Because Rh complexes have been shown to be excellent catalysts for enantioselective alkylation, olefination and allylation of pi systems through directed C-H functionalization under very mild conditions, this method has been seen to have broad synthetic potential both in organic chemistry and in biological systems. Moreover, selective conversion of ubiquitous C-H bonds into functional groups without intermediate preactivation is useful for shortening reaction sequences, with high environmental and economic benefits.
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页码:1459 / 1475
页数:17
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