Ayer et al., 1960 - Google Patents
The structure of lycodineAyer et al., 1960
View PDF- Document ID
- 7243863217288938918
- Author
- Ayer W
- Iverach G
- Publication year
- Publication venue
- Canadian Journal of Chemistry
External Links
Snippet
The molecular formula of the Lycopodium alkaloid lycodine has been revised to C16H22N2. Transformation of β-obscurine (I) into N-methyl lycodine has shown that lycodine is the pyridine analogue of des-N-methyl-β-obscurine and is represented by structure II (R= H) …
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 N1CCC[C@@H]2[C@H]3C[C@@H](C)C[C@]21C1=CC=CN=C1C3 0 title abstract description 67
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
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