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One-pot synthesis of (R)-convolutamydine A involving in situ chiral organocatalyst formation

2015-09-23T15:08:55Z (GMT) by Shengwei Wei Bernard Schmid Fliur Z. Macaev Serghei N Curlat Andrei Malkov Svetlana B. Tsogoeva
The application of a convenient one-pot synthetic strategy, utilizing an in situ formed organocatalyst, to the enantioselective synthesis of anti-leukaemia agent (R)-convolutamydine A has been demonstrated.

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