1995
DOI: 10.1080/10426509508042573
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Facile Synthesis of 4-Substituted 2-Pyrazolin-5-Ones Under Phase Transfer Catalysis

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Cited by 8 publications
(2 citation statements)
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“…In a plan to study C-versus O-alkylation of the pyrazoline derivatives, 3-methyl-1-phenyl-2-pyrazolin-5-one 333 was treated under PTC condition with different bromoorganic compounds such as benzyl bromide, 1,3-dibromopropane, methyl bromoacetate, bromoacetaldehyde, or diethylacetal as alkylating agents either in the absence or the presence of carbon disulphide and afforded numerous of C-or Oalkylated derivatives 334a-e, 335a-e [107] (Figure 119).…”
Section: C-alkylationmentioning
confidence: 99%
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“…In a plan to study C-versus O-alkylation of the pyrazoline derivatives, 3-methyl-1-phenyl-2-pyrazolin-5-one 333 was treated under PTC condition with different bromoorganic compounds such as benzyl bromide, 1,3-dibromopropane, methyl bromoacetate, bromoacetaldehyde, or diethylacetal as alkylating agents either in the absence or the presence of carbon disulphide and afforded numerous of C-or Oalkylated derivatives 334a-e, 335a-e [107] (Figure 119).…”
Section: C-alkylationmentioning
confidence: 99%
“…Sulphonylation. 4,5-Dihydro-3,5-diaryl-1-(4-fluorophenylsulphonyl)pyrazoles 341 and 2-aryl-1-(4-fluorphenylsulphonyl)indoles 343 were prepared from reaction of 4-fluorophenylsulphonyl chloride 339 with the appropriate 4,5-dihydro-3,5-diarylpyrazoles 340 or 2-arylindoles 342, via solid-liquid phase (THF/KOH/TBAB) [107] (Figure 121). N-Sulphonylation product 346 was prepared through treating 2-chloro-6,6-difluro-1,3-dioxolo[4,5-f]benzimidazole 344 with 3,5-dimethylisoxazole-4-sulphonyl chloride 345 via PTC protocol (toluene/aq.…”
Section: 2mentioning
confidence: 99%