Acid induced cationic rearrangements of carbocyclic compounds
This thesis examines fluorosulfonic acid as a reagent for use in organic synthesis. The acid strength of fluorosulfonic acid gives access to rearrangement products not available with weaker acids. The reaction of a selected series of benzyl carbinols with HSO₃F are reported. Reaction of 1-benzyl-2...
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| Language: | en |
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University of Canterbury. Chemistry
2013
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| Online Access: | http://hdl.handle.net/10092/7597 |