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JAPP Oxazole synthesis

JAPP Oxazole synthesis 187 JAPP KLINGEMANN Hydrazone synthesis 188 JAROUSSE MAKOSZA Phase transler 189 JEGERTetrahyikoturan synthesis 190 JOHNSON Phenol aHcynylation 191 Johnson 168,197,240 JONES Oxidation reagent 192 JULIA BRUYLANTS Cyclopropyl earbinol rearrangement 193... [Pg.225]

The Japp oxazole synthesis is the coupling of 1,2-diketones with ammonia and an aromatic aldehyde. The diketone contributes the C4 and C5 substituents, and the aromatic aldehyde contributes the C2 substituent. The synthesis also proceeds when reacting an a-ketooxime with a benzylic halide... [Pg.237]

The Japp oxazole synthesis is the reaction of 1,2-aromatic diketones 1 and aromatic aldedhyes in the presence of ammonia to form oxazoles... [Pg.233]


See other pages where JAPP Oxazole synthesis is mentioned: [Pg.187]    [Pg.327]    [Pg.176]    [Pg.706]    [Pg.328]    [Pg.237]    [Pg.238]    [Pg.238]    [Pg.213]    [Pg.233]    [Pg.695]    [Pg.727]    [Pg.817]    [Pg.176]    [Pg.685]   
See also in sourсe #XX -- [ Pg.187 ]

See also in sourсe #XX -- [ Pg.176 ]

See also in sourсe #XX -- [ Pg.237 ]

See also in sourсe #XX -- [ Pg.233 , Pg.234 , Pg.235 , Pg.236 , Pg.237 , Pg.238 , Pg.239 ]

See also in sourсe #XX -- [ Pg.176 ]




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