## Abstract The reaction of triphenylglycol (__S__)โ1 with thionyl chloride leads to the cyclic sulfites 2a and 2b in a ratio of 90:10. When the mixture of diastereomers 2a/b is treated with alcohols 3 or diols 6, enantiomerically pure ethers 5 and 7 are obtained by an unexpected S~N~1โtype ring cl
โฆ LIBER โฆ
Cyclic sulfite of 1,1'-dicyclohexyl-1,1'-diol
โ Scribed by Motevalli, M. ;Hursthouse, M. B. ;Hellier, D. G. ;Liddy, H. G.
- Book ID
- 114507555
- Publisher
- International Union of Crystallography
- Year
- 1990
- Tongue
- English
- Weight
- 226 KB
- Volume
- 46
- Category
- Article
- ISSN
- 0108-2701
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