Enantiopure Derivatives of 1,1,2-Triphenylethane-1,2-diol by Unusual Ring Opening of Its Cyclic Sulfite. -Reaction of the diastereomeric mixture (II) with the alcohols (III) or the diols (V) leads to the formation of the enantiomerically pure ethers via an SN1-type ring cleavage. Treatment of (II)
β¦ LIBER β¦
ChemInform Abstract: Efficient Resolution of (.+-.)-Pantolactone by Inclusion Crystallization with the Use of Chiral 1,1,2-Triphenylethane-1,2-diol.
β Scribed by M. G. Vinogradov; D. V. Kurilov; V. A. Ferapontov; G. L. Heise
- Publisher
- John Wiley and Sons
- Year
- 2001
- Weight
- 27 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0931-7597
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