On the dihydroxylation of cyclic allylic alcohols
The preparation and dihydroxylation (OsO 4) of a series of conformationally constrained allylic alcohols is described. By using dichloromethane as solvent, the selectivity that favours the anti triol is substantially reduced by hydrogen-bonding effects. This principle is appl...
| Main Authors: | , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
1996
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