Preparation and enantiomer recognition behaviour of azophenolic crown ethers containing cis-cyclohexane-1,2-diol as the chiral centre
โ Scribed by Naemura, Koichiro; Takeuchi, Sachiko; Hirose, Keiji; Tobe, Yoshito; Kaneda, Takahiro; Sakata, Yoshiteru
- Book ID
- 120975432
- Publisher
- Royal Society of Chemistry
- Year
- 1995
- Weight
- 617 KB
- Volume
- 3
- Category
- Article
- ISSN
- 1472-7781
No coin nor oath required. For personal study only.
๐ SIMILAR VOLUMES
Enantiomerically pure azophenolic crown ethers 1--4 containing (S)-or (R)l-phenylethane-l,2-diol moieties and (2S,4S)-2,4-dimethyl-3-oxapentane-l,5-diol moiety as a chiral subunit were prepared; crown ethers (S,S,S,S)-I showed high chiral recognition behaviour in complexation with 2-substituted 2-am
Preparation of Homochiral Azophenolic Crown Ethers Containing 1-Phenylethane-1,2-diol and 2,4,-Dimethyl-3-oxapentane-1,5-diol as a Chiral Subunit: Enantiomer Recognition Behavior Towards Chiral 2-Aminoethanol Derivatives. -The enantiomerically pure crown ethers (VII)-(X) are synthesized. Ether (VII