Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Nitrogen hydrides synthesis

Trimethylamine-alumimim hydride and trimethylamine-aluminum chloride dihydride, synthesis 9 Hexaureatitanium(III) perchlorate, s3Tithesis 12 Tetrasulfur tetranitride, synthesis 25 Sulfur nitrogen chlorides, synthesis 26... [Pg.56]

Hydroxypyrroles. Pyrroles with nitrogen-substituted side chains containing hydroxyl groups are best prepared by the Paal-Knorr cyclization. Pyrroles with hydroxyl groups on carbon side chains can be made by reduction of the appropriate carbonyl compound with hydrides, by Grignard synthesis, or by iasertion of ethylene oxide or formaldehyde. For example, pyrrole plus formaldehyde gives 2-hydroxymethylpyrrole [27472-36-2] (24). The hydroxymethylpyrroles do not act as normal primary alcohols because of resonance stabilization of carbonium ions formed by loss of water. [Pg.358]

Another useful route to alkaloids involves the electrochemical oxidation of lactams (145) bearing functionality on nitrogen that can be used to intramolec-ularly capture an intermediate acyl im-minium ion (146). The concept is portrayed in Scheme 33 and is highlighted by the synthesis of alkaloids lupinine (150) and epilupinine (151) shown in Scheme 34 [60]. Thus, the electrooxidation of lactam (147) provided a 71% yield of ether (148). Subsequent treatment with titanium tetrachloride affected cyclization and afforded the [4.4.0] bicyclic adduct (149). Krapcho decarbomethoxylation followed by hydride reduction of both the... [Pg.335]

A convenient method to affect the oxidation p- to nitrogen in piperidines is based on the anodic oxidation of N-carboalkoxy piperidines (Scheme 35). The electrochemical oxidation of piperidine (152) in the presence of acetic acid and potassium acetate, for example, afforded a mixture of isomeric 2-hydroxy-3-acetoxypiperidines (153) in a combined yield of 93%, following an aqueous workup [61]. Reduction with sodium boro-hydride severed the C-OH bond. Treatment with acid and then base completed a synthesis of pseudoconhydrine (154). [Pg.335]

Iron has a rich surface coordination chemistry that forms the basis of its important catalytic properties. There are many catalytic applications in which metallic iron or its oxides play a vital part, and the best known are associated with the synthesis of ammonia from hydrogen and nitrogen at high pressure (Haber-Bosch Process), and in hydrocarbon synthesis from CO/C02/hydrogen mixtures (Fischer-Tropsch synthesis). The surface species present in the former includes hydrides and nitrides as well as NH, NH2, and coordinated NH3 itself. Many intermediates have been proposed for hydrogenation of carbon oxides during Fischer-Tropsch synthesis that include growing hydrocarbon chains. [Pg.406]


See other pages where Nitrogen hydrides synthesis is mentioned: [Pg.80]    [Pg.416]    [Pg.45]    [Pg.42]    [Pg.112]    [Pg.30]    [Pg.163]    [Pg.119]    [Pg.124]    [Pg.64]    [Pg.339]    [Pg.650]    [Pg.11]    [Pg.232]    [Pg.1569]    [Pg.285]    [Pg.143]    [Pg.161]    [Pg.170]    [Pg.63]    [Pg.935]    [Pg.87]    [Pg.89]    [Pg.87]    [Pg.106]    [Pg.514]    [Pg.126]    [Pg.130]    [Pg.374]    [Pg.111]    [Pg.83]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.2 , Pg.2 , Pg.3 , Pg.4 , Pg.4 , Pg.4 , Pg.7 ]




SEARCH



Hydrides synthesis

Nitrogen hydrides

Nitrogen synthesis

© 2024 chempedia.info