Collective total synthesis of C4-oxygenated securinine-type alkaloids via stereocontrolled diversifications on the piperidine core.
- DOI
- 10.1038/s41467-022-32902-z
- Published
- 2022 Sep 2
- Container
- Nature communications
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1038/s41467-022-32902-z,
title = {Collective total synthesis of C4-oxygenated securinine-type alkaloids via stereocontrolled diversifications on the piperidine core.},
author = {Park S and Kang G and Kim C and Kim D and Han S},
year = {2022},
journal = {Nature communications},
doi = {10.1038/s41467-022-32902-z},
url = {https://doi.org/10.1038/s41467-022-32902-z}
}RIS
TY - JOUR TI - Collective total synthesis of C4-oxygenated securinine-type alkaloids via stereocontrolled diversifications on the piperidine core. AU - Park S AU - Kang G AU - Kim C AU - Kim D AU - Han S PY - 2022 JO - Nature communications DO - 10.1038/s41467-022-32902-z UR - https://doi.org/10.1038/s41467-022-32902-z ER -
APA
S, P., G, K., C, K., D, K., & S, H. (2022). Collective total synthesis of C4-oxygenated securinine-type alkaloids via stereocontrolled diversifications on the piperidine core.. Nature communications. https://doi.org/10.1038/s41467-022-32902-z
Source records
- pubmed · retrieved 2026-09-26T21:25:31.081Z