Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1367470 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
Gallium(III) chlorins possessing a series of axial ligands were synthesized as model compounds of natural chlorophylls. A pair of diastereomers arising from the fifth axial coordination onto the asymmetric chlorin π-macrocycle could be discriminated in a solution by both 1H- and 13C NMR spectroscopies.
Graphical abstractA pair of diastereomeric Ga(III) chlorophyll derivatives 1–4 arising from the fifth axial coordination onto the asymmetric chlorin π-macrocycle could be discriminated by NMR spectroscopy in solution.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shin-ichi Sasaki, Tadashi Mizoguchi, Hitoshi Tamiaki,