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: | Donohoe, T, Garg, R, Moore, P |
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Format: | Journal article |
Language: | English |
Published: |
1996
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