Khalid et al., 2017 - Google Patents
1, 2, 3-Benzotriazin-4 (3H)-ones: Synthesis, reactions and applicationsKhalid et al., 2017
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- 9460496704763692547
- Author
- Khalid Z
- Ahmad H
- Munawar M
- Khan M
- Gul S
- Publication year
- Publication venue
- Heterocycles
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1,2,3-BENZOTRIAZIN-4(3H)-ONES: SYNTHESIS, REACTIONS AND APPLICATIONS Zunera
Khalid, Hafiz Adnan Ahmad, Munawar Ali Munawar,* Mis Page 1 HETEROCYCLES, Vol. 94,
No. 1, 2017, pp. 3 - 54. © 2017 The Japan Institute of Heterocyclic Chemistry Received, 12th …
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 C1=CC=C2C(=O)N=NNC2=C1 0 title abstract description 124
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- C07D243/10—Heterocyclic compounds containing seven-membered rings having two nitrogen atoms as the only ring hetero atoms having the nitrogen atoms in positions 1,4 condensed with carbocyclic rings or ring systems
- C07D243/14—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines
- C07D243/16—1,4-Benzodiazepines; Hydrogenated 1,4-benzodiazepines substituted in position 5 by aryl radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/04—Ortho-condensed systems
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- C—CHEMISTRY; METALLURGY
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- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
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- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
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- 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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- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
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