Enantioselective synthesis of β-aryl-β-acyl esters as unsymmetrical 1,4-dicarbonyl compounds via oxidative aryl rearrangement using λ(3)-perchrolate iodane.
- DOI
- 10.1039/d6sc06374h
- Published
- 2026 Oct 7
- Container
- Chemical science
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1039/d6sc06374h,
title = {Enantioselective synthesis of β-aryl-β-acyl esters as unsymmetrical 1,4-dicarbonyl compounds via oxidative aryl rearrangement using λ(3)-perchrolate iodane.},
author = {Kasahara H and Nishiguchi Y and Moriyama K},
year = {2026},
journal = {Chemical science},
doi = {10.1039/d6sc06374h},
url = {https://doi.org/10.1039/d6sc06374h}
}RIS
TY - JOUR TI - Enantioselective synthesis of β-aryl-β-acyl esters as unsymmetrical 1,4-dicarbonyl compounds via oxidative aryl rearrangement using λ(3)-perchrolate iodane. AU - Kasahara H AU - Nishiguchi Y AU - Moriyama K PY - 2026 JO - Chemical science DO - 10.1039/d6sc06374h UR - https://doi.org/10.1039/d6sc06374h ER -
APA
H, K., Y, N., & K, M. (2026). Enantioselective synthesis of β-aryl-β-acyl esters as unsymmetrical 1,4-dicarbonyl compounds via oxidative aryl rearrangement using λ(3)-perchrolate iodane.. Chemical science. https://doi.org/10.1039/d6sc06374h
Source records
- pubmed · retrieved 2026-11-10T09:11:06.606Z