Paronikyan et al., 2003 - Google Patents
Synthesis ad Some Conversions of Partially Hydrogenated 1-Aminopyrano (thiopyrano)[4, 3-d] pyrazolo [3, 4-b] pyridines and Pyrazolo [3, 4-c] isoquinolinesParonikyan et al., 2003
- Document ID
- 12521898444392749131
- Author
- Paronikyan E
- Sirakanyan S
- Noravyan A
- Publication year
- Publication venue
- Chemistry of Heterocyclic Compounds
External Links
Snippet
Synthesis ad Some Conversions of Partially Hydrogenated 1-Aminopyrano(thiopyrano)[4,3-<Emphasis
Type="Italic">d& Page 1 Chemistry of Heterocyclic Compounds, Vol. 39, No. 3, 2003
SYNTHESIS AND SOME CONVERSIONS OF PARTIALLY HYDROGENATED 1-AMINOPYRANO(THIOPYRANO)[4,3-d] …
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 C1=CC=C2C3=CNN=C3N=CC2=C1 0 title abstract 2
Classifications
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- C07D493/02—Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
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- C—CHEMISTRY; METALLURGY
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D475/00—Heterocyclic compounds containing pteridine ring systems
- C07D475/02—Heterocyclic compounds containing pteridine ring systems with an oxygen atom directly attached in position 4
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