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While this work was in progress, Ciufolini and Sorenson independently reported complementary methods for preparing spirocyclic pyrrolidinones involving the oxidation of phenolic oxazolines, and amines, respectively. These transformations involve aryl oxidation and subsequent trapping rather than the formation of N-acylnitrenium ions: (a) Braun, N. A.; Ousmer, M.; Bray, J. D.; Bouchu, D.; Peters, K.; Peters, E. M.; Ciufolini, M. A. J. Org. Chem. 2000, 65, 4397-4408.
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note
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2 alone led to lower yields of 10.
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36
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0041788319
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note
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9a work, was not observed with our spriocyclic system.
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37
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0031562437
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43
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0042289394
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note
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9 -8.1° (c 0.42, MeOH)).
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