Rhodium(II)-catalysed tandem aziridination and ring-opening: stereoselective synthesis of functionalised tetrahydrofurans.
Aziridines formed upon treatment of allylic carbamates and homoallylic sulfamates with Rh(II) carboxylate catalysts under oxidative conditions are trapped by suitably-disposed hydroxyl groups to give functionalised tetrahydrofurans.
Main Authors: | Unsworth, W, Clark, N, Ronson, T, Stevens, K, Thompson, A, Lamont, S, Robertson, J |
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Format: | Journal article |
Language: | English |
Published: |
2014
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