Metal-mediated aminocatalysis provides mild conditions: Enantioselective Michael addition mediated by primary amino catalysts and alkali-metal ions
- DOI
- 10.3762/bjoc.9.18
- Published
- 2013-01-23
- Container
- Beilstein Journal of Organic Chemistry
- Publisher
- Beilstein Institut
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.3762/bjoc.9.18,
title = {Metal-mediated aminocatalysis provides mild conditions: Enantioselective Michael addition mediated by primary amino catalysts and alkali-metal ions},
author = {Matthias Leven and Jörg M Neudörfl and Bernd Goldfuss},
year = {2013},
journal = {Beilstein Journal of Organic Chemistry},
doi = {10.3762/bjoc.9.18},
url = {https://doi.org/10.3762/bjoc.9.18}
}RIS
TY - JOUR TI - Metal-mediated aminocatalysis provides mild conditions: Enantioselective Michael addition mediated by primary amino catalysts and alkali-metal ions AU - Matthias Leven AU - Jörg M Neudörfl AU - Bernd Goldfuss PY - 2013 JO - Beilstein Journal of Organic Chemistry DO - 10.3762/bjoc.9.18 UR - https://doi.org/10.3762/bjoc.9.18 ER -
APA
Leven, M., Neudörfl, J. M., & Goldfuss, B. (2013). Metal-mediated aminocatalysis provides mild conditions: Enantioselective Michael addition mediated by primary amino catalysts and alkali-metal ions. Beilstein Journal of Organic Chemistry. https://doi.org/10.3762/bjoc.9.18
Source records
- crossref · retrieved 2026-09-26T05:01:43.357Z