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Concise stereoselective syntheses of (+)‐α‐conhydrine and its pyrrolidine analogue are described. The key features are a highly diastereoselective chelation‐controlled hydride reduction of the amino ketone, to give the anti amino alcohol directly, and an intramolecular ring‐closing metathesis.
Asian Journal of Organic Chemistry – Wiley
Published: Nov 1, 2012
Keywords: ; ; ; ;
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