Author:
Wei Shengwei,Schmid Bernhard,Macaev Fliur Z.,Curlat Serghei N.,Malkov Andrei V.,Tsogoeva Svetlana B.
Abstract
Abstract
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.
Cited by
4 articles.
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