| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1348302 | Tetrahedron: Asymmetry | 2011 | 7 Pages |
Abstract
Chiral rhombamine macrocycles 1a–b were prepared by a [2+2]cyclocondensation reaction of (R,R)-1,2-diaminocyclohexane with corresponding dialdehydes and were found to be useful as NMR chiral shift reagents for the determination of enantiomeric purity and the absolute configuration of a wide range of carboxylic acid and amino acid derivatives.
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Related Topics
Physical Sciences and Engineering
Chemistry
Inorganic Chemistry
Authors
Koichi Tanaka, Yuki Nakai, Hiroki Takahashi,