WEI, S. ... et al, 2015. One-pot synthesis of (R)-convolutamydine A involving in situ chiral organocatalyst formation. Asymmetric Catalysis, 2 (1), pp. 1 - 6.
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.
This is an Open Access article published by De Gruyter Open and licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.
S.B.T is grateful to the
Interdisciplinary Center for Molecular Materials (ICMM),
Erlangen Catalysis Resource Center (ECRC) and Deutsche
Forschungsgemeinschaft (DFG) for research support.
S.B.T. and F.Z.M. acknowledge financial support from the
BMBF and AȘM (bilateral BMBF-AȘM project Ref. № MDA
08/010 and № 09.820.05.08 GF).