TY - JOUR
T1 - Asymmetric catalysis with bis(hydroxyphenyl)diamides/rare-earth metal complexes
AU - Kumagai, Naoya
AU - Shibasaki, Masakatsu
PY - 2013/1/2
Y1 - 2013/1/2
N2 - A series of asymmetric catalysts composed of conformationally flexible amide-based chiral ligands and rare-earth metals was developed for proton-transfer catalysis. These ligands derived from amino acids provide an intriguing chiral platform for the formation of asymmetric catalysts upon complexation with rare-earth metals. The scope of this arsenal of catalysts was further broadened by the development of heterobimetallic catalytic systems. The cooperative function of hydrogen bonding and metal coordination resulted in intriguing substrate specificity and stereocontrol, and the dynamic nature of the catalysts led to a switch of their function. Herein, we summarize our recent exploration of this class of catalysts.
AB - A series of asymmetric catalysts composed of conformationally flexible amide-based chiral ligands and rare-earth metals was developed for proton-transfer catalysis. These ligands derived from amino acids provide an intriguing chiral platform for the formation of asymmetric catalysts upon complexation with rare-earth metals. The scope of this arsenal of catalysts was further broadened by the development of heterobimetallic catalytic systems. The cooperative function of hydrogen bonding and metal coordination resulted in intriguing substrate specificity and stereocontrol, and the dynamic nature of the catalysts led to a switch of their function. Herein, we summarize our recent exploration of this class of catalysts.
KW - Amides
KW - Asymmetric catalysis
KW - Atom economy
KW - Heterobimetallic
KW - Rare earths
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U2 - 10.1002/anie.201206582
DO - 10.1002/anie.201206582
M3 - Review article
C2 - 23180601
AN - SCOPUS:84871944941
SN - 1433-7851
VL - 52
SP - 223
EP - 234
JO - Angewandte Chemie - International Edition
JF - Angewandte Chemie - International Edition
IS - 1
ER -