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Dehalogenation/dehydrogenative

SCHEME 43.5. Lee et al. s stereoselective radical dehalogenation/dehydrogenative cycUzation. [Pg.1305]

Catalysts. In industrial practice the composition of catalysts are usuaUy very complex. Tellurium is used in catalysts as a promoter or stmctural component (84). The catalysts are used to promote such diverse reactions as oxidation, ammoxidation, hydrogenation, dehydrogenation, halogenation, dehalogenation, and phenol condensation (85—87). Tellurium is added as a passivation promoter to nickel, iron, and vanadium catalysts. A cerium teUurium molybdate catalyst has successfliUy been used in a commercial operation for the ammoxidation of propylene to acrylonitrile (88). [Pg.392]

Dehalogenating reduction Salt elimination Disproportionation Electrochemical formation Dehydrogenative catalytic coupling... [Pg.276]

The procedure described is essentially that of Ballard and Dehn.1 Stilbene has also been prepared by reduction of desoxy-benzoin,20 benzaldehyde,23 and benzil 2o-2c by dehydrogenation of ethyl benzene,30 toluene,30- 33- 3, and bibenzyl 33-3alkaline reduction of phenylnitromethane,40 phenylnitroacetonitrile,40 and desoxybenzoin 43 by distillation of benzyl sulfone,50 benzyl sulfide,60-63 calcium cinnamate,5 cinnamic acid,5d phenyl cinna-mate,6e-6/ and diphenyl fumarate ie by dehydrohalogenation of a,a -dichlorobibenzyl60 and benzyl chloride 63 by dehalogenation of a,a,c/,a -tetrachlorobibenzyl70 and benzal chloride 73 by the coupling of cinnamic acid and phenyldiazonium chloride 8 by de-... [Pg.107]

The methylamination is less selective. This lower selectivity is due to the stronger nucleophilicity of methylamine as also shown by the methylamino-dehalogenation occurring with 2-chloro-5-nitroquinoxaline and 2-chloro-7-nitroquinoxaline into 2-amino-5-nitroquinoxaline and 2-amino-7-nitroquinoxaline, respectively. Amino-dehydrogenations with these compounds were not observed (see Scheme 22). It is important to note that 5-nitroquinoxaline gives methylamination at position ortho and para... [Pg.21]


See other pages where Dehalogenation/dehydrogenative is mentioned: [Pg.172]    [Pg.172]    [Pg.172]    [Pg.172]    [Pg.200]    [Pg.372]    [Pg.279]    [Pg.34]    [Pg.45]    [Pg.436]    [Pg.282]    [Pg.26]    [Pg.26]    [Pg.202]    [Pg.224]    [Pg.1361]    [Pg.660]    [Pg.99]    [Pg.78]    [Pg.142]    [Pg.1053]   


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Dehalogenation

Dehalogenation and Dehydrogenation Mediated by NHC-Ni Complexes

Dehalogenations

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