Bakavoli et al., 2005 - Google Patents
Synthesis of optically active imidazo [1, 2-a] pyrimidin-3 (2H)-onesBakavoli et al., 2005
- Document ID
- 10315420453363741439
- Author
- Bakavoli M
- Bagherzadeh G
- Rahimizadeh M
- Publication year
- Publication venue
- Mendeleev Communications
External Links
Snippet
The reactions of 2-chloro-4-(substituted amino)-6-methyl-5-nitropyrimidine 1 with (L)-α- amino acids gave substituted derivatives 3, which were converted to optically active imidazo [1, 2-a] pyrimidines 4 by treatment with either phosphorus oxychloride or polyphosphoric …
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 N1=CC=CN2C(=O)CN=C21 0 title description 2
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
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