A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro.
- DOI
- 10.1016/s0960-894x(00)00110-4
- Published
- 2000 Apr 17
- Container
- Bioorganic & medicinal chemistry letters
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/s0960-894x-00-00110-4,
title = {A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro.},
author = {Larget R and Lockhart B and Renard P and Largeron M},
year = {2000},
journal = {Bioorganic \& medicinal chemistry letters},
doi = {10.1016/s0960-894x(00)00110-4},
url = {https://doi.org/10.1016/s0960-894x(00)00110-4}
}RIS
TY - JOUR TI - A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro. AU - Larget R AU - Lockhart B AU - Renard P AU - Largeron M PY - 2000 JO - Bioorganic & medicinal chemistry letters DO - 10.1016/s0960-894x(00)00110-4 UR - https://doi.org/10.1016/s0960-894x(00)00110-4 ER -
APA
R, L., B, L., P, R., & M, L. (2000). A convenient extension of the Wessely-Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro.. Bioorganic & medicinal chemistry letters. https://doi.org/10.1016/s0960-894x(00)00110-4
Source records
- pubmed · retrieved 2026-09-26T08:18:50.660Z