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NaOMe

NaBH4. See borohydrides. Prepared NaOMe plus B2H6. Used in organic reduc-... [Pg.362]

Chloro-2-(ethoxycarbonyl)-3-(4-fluorophenyl) N-[5-Chloro-2-(4-fluorobenzoyl]benzamide, methyl bromoacetate (1) NaH (2) NaOMe 30 [2]... [Pg.31]

A solution of NaOMe was prepared from sodium (4.35 g, 0.19 g-atom) and MeOH (300 ml). This was added to a stirred solution of gramine (30 g. [Pg.122]

If the fV-aryl group is strongly activated, then it can be removed in nucleophilic substitution reactions in which the azole anion acts as leaving group. Thus l-t2,4-dinitrophenyl)pyrazole reacts with N2H4 or NaOMe. [Pg.108]

See other pages where NaOMe is mentioned: [Pg.21]    [Pg.276]    [Pg.411]    [Pg.108]    [Pg.178]    [Pg.61]    [Pg.73]    [Pg.73]    [Pg.84]    [Pg.141]    [Pg.141]    [Pg.143]    [Pg.157]    [Pg.267]    [Pg.271]    [Pg.287]    [Pg.328]    [Pg.224]    [Pg.76]    [Pg.90]    [Pg.120]    [Pg.120]    [Pg.124]    [Pg.58]    [Pg.208]    [Pg.223]    [Pg.105]    [Pg.105]    [Pg.124]    [Pg.127]    [Pg.137]    [Pg.145]    [Pg.151]    [Pg.140]    [Pg.141]    [Pg.29]    [Pg.29]    [Pg.40]    [Pg.76]    [Pg.102]    [Pg.103]    [Pg.74]    [Pg.109]    [Pg.126]    [Pg.188]    [Pg.4]    [Pg.65]   
See also in sourсe #XX -- [ Pg.248 , Pg.706 ]

See also in sourсe #XX -- [ Pg.136 ]

See also in sourсe #XX -- [ Pg.166 , Pg.272 ]

See also in sourсe #XX -- [ Pg.389 ]

See also in sourсe #XX -- [ Pg.60 , Pg.61 ]



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