Journal of the American Chemical Society · 2015 · 100 citations · 64 references
Natural SciencesChemistryMedicinal ChemistryDrug DiscoveryInorganic ChemistrySynthetic Medicinal ChemistryChiral RecognitionChiral SeparationCoordination ChemistryMetal-ligand BondingTransition Metal ComplexesChiralityChirality DeterminationNonpolar SolventsOctahedral ComplexesOctahedral CoordinationSolvent CompatibilitySubstrate ScopeSubstrate Scope Expansion
Chiral analysis, such as determination of identity, concentration, and relative ratio of optically active (chiral) molecules, plays an indispensable role in contemporary synthetic, medicinal, and biological chemistry. Here, we describe the selective control of metal-centered chirality in an octahedral geometry to prepare negatively charged Al(III) complexes, which can be used as versatile (1)H NMR chiral solvating agents for both positively and negatively charged chiral molecules in polar or nonpolar solvents. During the formation of ion pairs between the Al(III) complexes and the chiral analytes such as amines and carboxylic acids, the metal-centered chirality in the Al complexes plays a crucial role in providing anisochronous chemical shifts to the (1)H NMR spectra. As a chiral solvating agent, Al(III) complexes display an unprecedentedly broad substrate scope, good solvent compatibility, and operational simplicity.
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Asymmetric photoredox transition-metal catalysis activated by visible light
Haohua Huo, Xiaodong Shen, Chuanyong Wang et al. · Nature · 2014 · 625 citations