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The article presents chemical equations for article "Asymmetric Diboration of Terminal Alkenes with a Rhodium Catalyst and Subsequent Oxidation: Enantioselective Synthesis of Optically Active 1,2-Diols" by K. Toribatake and others, published in "Angewandte Chemie International Edition" in 2013.

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.

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]

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]

The one-pot reaction consisting of an alkynylation and successive aldol reaction provides various novel α-propargyl group containing β-hydroxyketone derivatives in high yields. [ABSTRACT FROM AUTHOR]

10 examples [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]

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]

Chiral rhodium[bis(oxazolinyl)phenyl] complexes exhibit high catalytic activity for the enantioselective β-boration of α,β-unsaturated esters, ketones, and amides. [ABSTRACT FROM AUTHOR]

RHC efficiently promotes the asymmetric hydrosilylation of 3,3-diarylacrylates. [ABSTRACT FROM AUTHOR]

Regio- and enantioselective hydrosilylation of alkenes is achieved using triethoxysilane in the presence of a chiral Rh-complex catalyst. [ABSTRACT FROM AUTHOR]