4.7 Article

From Cationic to Anionic Helicenes: New Reactivity through Umpolung

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JOURNAL OF ORGANIC CHEMISTRY
卷 76, 期 8, 页码 2716-2722

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AMER CHEMICAL SOC
DOI: 10.1021/jo200071n

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  1. Swiss National Science Foundation

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Using a two-step reduction/metalation procedure, highly stable chiral carbenium ions are transformed into reactive carbanion intermediates. Interesting polar ketone and thioamide products are the results of this umpolung that occurs with complete retention of configuration of the helical backbone.

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