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2-Nitromethyl-4,5-dihydro

Benzo[c)-l,2-oxaborol l-Hydroxy-3-nitromethyl-1,3-dihydro- XIII/ 3a, 793... [Pg.467]

Benzoesaure 2-Hydroxy-5-(3-oxo-butanoylamino)- XI/2, 20 2-Benzofuran 6,7-Dimethoxy-3-nitromethyl-1-oxo-1,3-dihydro-VI/2, 576 Bernsteinsanre Benzoylamino- IV/lb, 644 2-(2-Hydroxy-benzylidenamino)- XI/ 2, 327... [Pg.866]

Oxazol (5R)-5-Methyl-5-nitromethyl-3-phenyl-4,5-dihydro- E16d, 243 (Allyl-N02 + R-CNO)... [Pg.876]

Several other ketones were employed as starting material. Pyridazines were obtained from y-nitroketones and hydrazine. The initially formed 4,5-dihydro-3(2H)-pyridazinone oximes (4) are transformed with dilute acid into 5.58 The reaction is postulated to proceed via a nitrile oxide, generated from the nitromethyl group. [Pg.367]

O-Nitro-O-nitromethyl-fluoren 5 II652. [10-Nitro-9.10-dihydro-anthtanyl-(9)]-nitrit 6, 608. [Pg.2386]

See other pages where 2-Nitromethyl-4,5-dihydro is mentioned: [Pg.148]    [Pg.154]    [Pg.427]    [Pg.129]    [Pg.136]    [Pg.148]    [Pg.368]    [Pg.61]    [Pg.71]    [Pg.154]    [Pg.367]    [Pg.32]   
See also in sourсe #XX -- [ Pg.148 ]



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2-Nitromethyl

Nitromethylation

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