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Hydrogen reagent

A basic process flow diagram for the SNCR TDN process is shown in Figure 17.3. Anhydrous or aqueous ammonia is vaporized and mixed with a carrier gas of air or steam for transport to injection/distribution modules. The injection distribution modules distribute ammonia and/or hydrogen reagent and carrier gas to proprietary spray nozzles or injection lances. Reagent flow control can be controlled and trimmed by outlet NOx signals or ammonia slip measurements. [Pg.322]

The carbocation subsequently is quenched by a hydride donor or hydrogen to yield the saturated product. A sufficient stability of the intermediate carbocation and proper choice of the hydrogenating reagent pair are prerequisites to a successful ionic hydrogenation. [Pg.650]

Fig. 6.6 COSY spectrum of C3v C6QH18 produced in high yield using diethylenetriamine as both solvent and hydrogenation reagent (Briggs et al. 2005). The weak cross-peak between protons A and B corresponds to a SJHH of 3 Hz. Asterisks indicate residual solvent (quartet) and a minor impurity (singlet)... Fig. 6.6 COSY spectrum of C3v C6QH18 produced in high yield using diethylenetriamine as both solvent and hydrogenation reagent (Briggs et al. 2005). The weak cross-peak between protons A and B corresponds to a SJHH of 3 Hz. Asterisks indicate residual solvent (quartet) and a minor impurity (singlet)...
Scheme 16. Domino hydroformylation-Wittig olefination-hydrogenation. Reagents and conditions 1.5 Equiv. Scheme 16. Domino hydroformylation-Wittig olefination-hydrogenation. Reagents and conditions 1.5 Equiv.
Scheme 17. Domino hydroformylation-Knoevenagel condensation-hydrogenation. Reagents and conditions 1.1 Equiv. CH2EWG2, 1.2 equiv. piperidinium acetate, 0.7 mol% [Rh(CO)2acac], 2.8 mol%... Scheme 17. Domino hydroformylation-Knoevenagel condensation-hydrogenation. Reagents and conditions 1.1 Equiv. CH2EWG2, 1.2 equiv. piperidinium acetate, 0.7 mol% [Rh(CO)2acac], 2.8 mol%...
Figure 20. Stereoselective synthesis of naproxen and ibuprofen by hydrogenation. Reagents a, C02, electrolysis b, H30 + c, H +, -H20 d, H2, Ru(acac)2/BINAP. Figure 20. Stereoselective synthesis of naproxen and ibuprofen by hydrogenation. Reagents a, C02, electrolysis b, H30 + c, H +, -H20 d, H2, Ru(acac)2/BINAP.
Cleavage protocols for the release of aliphatic molecules are very common [273,274]. There exist, for example, procedures for photolabile linkers, linkers that are thermally cleavable and linkers that release target structures upon addition of hydrogenating reagents. Linkers for these methodologies are of a different nature as a result of their need to fulfil special demands. [Pg.45]


See other pages where Hydrogen reagent is mentioned: [Pg.229]    [Pg.433]    [Pg.822]    [Pg.286]    [Pg.1309]    [Pg.98]    [Pg.134]    [Pg.447]    [Pg.447]    [Pg.229]    [Pg.152]    [Pg.152]    [Pg.133]    [Pg.91]    [Pg.61]    [Pg.172]    [Pg.198]    [Pg.734]    [Pg.865]    [Pg.626]    [Pg.199]   
See also in sourсe #XX -- [ Pg.307 ]




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