Wiley-VCH Verlag, ChemInform, 42(34), 2003
Elsevier, Bioorganic and Medicinal Chemistry Letters, 14(13), p. 2389-2391
DOI: 10.1016/s0960-894x(03)00397-4
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Open D-ring galanthamine analogues were prepared using ring-opening reactions of the quaternarized urethane or oxazolidine functions and were evaluated for their acetylcholinesterase (AChE) and butyrylcholinesterase (BChE) inhibition potency.