One-pot synthesis of (R)-convolutamydine A involving in situ chiral organocatalyst formation
journal contribution
posted on 2015-09-23, 15:08 authored by Shengwei Wei, Bernard Schmid, Fliur Z. Macaev, Serghei N Curlat, Andrei MalkovAndrei Malkov, Svetlana B. TsogoevaThe 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.
Funding
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).
History
School
- Science
Department
- Chemistry
Published in
Asymmetric CatalysisVolume
2Issue
1Pages
1 - 6 (6)Citation
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.Publisher
De Gruyter Open / © The AuthorsVersion
- VoR (Version of Record)
Publisher statement
This work is made available according to the conditions of the Creative Commons Attribution-NonCommercial-NoDerivatives 3.0 Unported (CC BY-NC-ND 3.0) licence. Full details of this licence are available at: http://creativecommons.org/licenses/by-nc-nd/3.0/Publication date
2015Notes
This is an Open Access article published by De Gruyter Open and licensed under the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 License.eISSN
2300-4630Publisher version
Language
- en
