Induction of axially chiral N-C bonds in N-aryl acridane and related complexes by chromium tricarbonyl migration reactions.

The thermal chromium tricarbonyl migration reaction induced axially chiral N-C bonds of N-aryl acridane and related complexes in good yield with outstanding enantiomeric excess.

Induction of one-handed helical oligo(p-benzamide)s by domino effect based on planar-axial-helical chirality relay.

One-handed helical oligo(p-benzamide)s were induced via the domino effect based on the planar-axial-helical chirality relay triggered by a planar chiral transition-metal complex at the terminal position as the single chiral source.

Stereoselective synthesis of both enantiomers of N-aryl indoles with axially chiral N-C bonds.

N-Aryl indoles with axially chiral N-C bonds were synthesized by stereoselective nucleophilic aromatic substitution reactions of planar chiral tricarbonyl(2,6-disubstituted-1-fluorobenzene)chromium complexes. The stereochemistry of the products is highly dependent on the position of the substituent in the indole. When indoles devoid of a substituent at the 2-position were used, N-aryl indole chromium complexes having anti orientation with respect to the tricarbonylchromium fragment were obtained diastereoselectively.

Highly emissive pi-conjugated alkynylpyrene oligomers: their synthesis and photophysical properties.

We newly prepared para- and meta-linked alkynylpyrene oligomers and examined their photophysical properties. Oligomerization of monomeric building blocks was performed by CuI-promoted oxidative coupling reaction. The resulting oligomers mainly consist of 2-mer to 6-mer that were assigned on the basis of MALDI-TOF mass spectra, and the 2-mer, 3-mer, and 4-mer were isolated and fully characterized.