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An abstract of the article "Nickel(II)-Catalyzed Asymmetric Michael Addition of Oxindoles With Modified N,N,O-Tridentate Chiral Phenanthroline Ligands" by Y. Naganawa, H. Abe and H. Nishiyama is presented.

An abstract of the article "Nickel(II)-Catalyzed Asymmetric Michael Addition of Oxindoles with Modified N,N,O-Tridentate Chiral Phenanthroline Ligands" by Yuki Nagawana and colleagues are presented.

The article presents chemical equations for the article "Cu(II)-Catalyzed Enantioselective α-Hydroxylation and α-Chlorination of β-Ketoesters with N,N,O-Tridentate Chiral Phenanthroline Ligand" by Y. Naganawa and others published in "ChemistrySelect" in 2016.

An enantioselective conjugate hydrosilylation of prochiral γ,γ-disubstituted cyclohexadienones furnishes cyclohexenones with a chiral quaternary γ-carbon atom. [ABSTRACT FROM AUTHOR]

Zinc-catalyzed asymmetric α-amination of various cyclic β-ketocarbonyl compounds using azodicarboxylate (II) as the electrophilic nitrogen source is described. [ABSTRACT FROM AUTHOR]

An asymmetric oxygen atom transfer of oxindole derivatives using Davis′ oxaziridine gives the corresponding 3-aryl-3-hydroxy-2-oxindole derivatives with excellent enantioselectivity. [ABSTRACT FROM AUTHOR]

10 examples [ABSTRACT FROM AUTHOR]

Design of the novel type of axially chiral ligand (BPT) is based on the concept of innovation utilizing phenanthroline units which has superior coordination ability with a wide range of metal ions. [ABSTRACT FROM AUTHOR]

The scalable one-pot title reaction allows for the transformation of N-acyl protected amines including imides, amides, and carbamates, bearing a terminal allyl group or, for the first time, a 1,2-substituted E-alkene moiety. [ABSTRACT FROM AUTHOR]