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ChemInform Abstract: Preparation of Optically Active Azophenolic Crown Ethers Containing 1-Phenylethane-1,2-diol and 2,4-Dimethyl-3-oxapentane-1,5-diol as a Chiral Subunit (I)—(IV): Temperature-Dependent Enantiomer Selectivity in the Complexation with Chiral Amines.

✍ Scribed by K. OGASAHARA; K. HIROSE; Y. TOBE; K. NAEMURA


Publisher
John Wiley and Sons
Year
2010
Weight
31 KB
Volume
29
Category
Article
ISSN
0931-7597

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ChemInform Abstract: Preparation of Homo
✍ K. NAEMURA; K. OGASAHARA; K. HIROSE; Y. TOBE 📂 Article 📅 2010 🏛 John Wiley and Sons ⚖ 33 KB

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