A convenient extension of the Wessely–Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro - Concepedia

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A convenient extension of the Wessely–Moser rearrangement for the synthesis of substituted alkylaminoflavones as neuroprotective agents in vitro

DOI Full Paper Access

118

Citations

17

References

2000

Year

Ronan Larget, Brian Lockhart, Pierre Renard, Martine Largeron

Bioorganic & Medicinal Chemistry Letters

Wessely–moser RearrangementBioorganic ChemistrySubstituted AlkylaminoflavonesPharmacologyPharmaceutical ChemistryConvenient ExtensionBiomolecular EngineeringNatural Product Synthesis

References

	Year	Citations

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