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- W2006792014 abstract "An analogue of adenine 3, in which the aminopyrimidine moiety is annulated to a cyclopentadienyl ring of ferrocene, was synthesized from ferrocenecarboxaldehyde. The key intermediate in this synthesis was 2-aminoferrocenenitrile, which was prepared regio- and stereoselectively. An X-ray crystallographic structure study of 6, a derivative of 3 obtained by acetylation, confirmed the structure of the product." @default.
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- W2006792014 date "2000-12-01" @default.
- W2006792014 modified "2023-09-27" @default.
- W2006792014 title "Synthesis of a redox active analogue of adenine" @default.
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- W2006792014 doi "https://doi.org/10.1016/s0040-4039(00)01703-2" @default.
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