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One-pot synthesis of(R)-convolutamydineA involvingin situchiral organocatalyst formation

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Wei S., Schmid B., Macaev F. Z., Curlat S. N., 1, Malkov A. V., Tsogoeva S. B.
Asymmetric Catalysis
|
2015
|
vol. 2
|
issue 1
EN
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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