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Catalysts procedures

From the point of view of efficiency and application to the industrial production of optically pure compounds the chiral catalyst procedure is the methodology of choice. In this context. Sharpless asymmetric epoxidation and dihydroxylation, Noyori-Takaya s second generation asymmetric hydrogenations and Jacobsen s epoxidation [3] have had a tremendous impact in the last few years and they constitute the basis of the newly spawned "chirotechnology" firms, as well as of the pharmaceutical, fine chemical and agriculture industries. [Pg.294]

Carreira and coworkers have established silanolates as useful nucleophiles [70], with aUylic substitutions being carried out with an activated catalyst [procedure (c). [Pg.242]

Low-temperature solution polycondensation in NMP, followed by catalytic imidisation of the polyamic acids formed in reaction solutions using a pyridine-acetic anhydride (1 1) complex as catalyst (procedure 1) ... [Pg.50]

High-temperature solution polycondensation in w-cresol using isoquinoline as catalyst (procedure 3). [Pg.50]

Although the action of bromine on tetralin readily yields hydrogen bromide, 50 per cent of the bromine is lost in its combination with the organic molecule. Where larger quantities of hydrogen bromide for production of hydro-bromic acid are required, it is advisable to make use of the method of direct combination of hydrogen and bromine, using a suitable catalyst (procedure B).1,5,6... [Pg.151]

Screens of precisely calibrated mesh sizes and openings are the principal devices for measuring the distribution of sizes for particulate catalysts. Procedures are discussed in Section II.B.l. [Pg.109]

Regeneration consists of (i) removal of inhibiting substances IS sometimes poisons, most often inhibitors or fouling agents, c.g., coke (ii) redispersion of the active species, or (iii) both. Regeneration procedures are often specific to the catalyst and the species causing deactivation. With respect to regeneration, procedures arc described precisely by catalyst manufacturers, for each type of important industrial catalyst. Procedures for... [Pg.572]

Condensation catalyst. Procedures for the condensation of malonic acid with furfural and with m-nitrobenzaldehyde are outlined in the formulations. The first uses more pyridine than the second and no other solvent, and the reaction period is... [Pg.1213]

Alkoxy substituents are also able to direct additions to 5-alkoxy-2(5//)-furanone44. In the following modified nickel catalyst procedure, attack of methylenecyclopropane occurs once again from the sterically least hindered face. However, the yield is poor and a mixture of type A and type B products is obtained. For comparison, the type A product obtained here as the minor isomer is the sole product observed in the TMM-Pd-mediated transformation19a. [Pg.843]

This method has been developed largely by Klemm et al. and is discussed in a recent review,7 which gives details on catalysts, procedure, and possible mechanisms Examples include formation of the peri-condensed compounds 35 (29-39%), from bridging at positions 4 and 5 of the phenanthrene molecule 149 at ca. 630°C in the presence of various sulfided mixed metallic oxide catalysts,6,36 and 80 (18%), from similar bridging in the triphenylene molecule 150 at 500°C.37 Since the sulfur bridge forms by substitution at the sterically most hindered positions of these hydrocarbon substrates, method... [Pg.165]

Two-catalyst procedures have also been developed, which use both acid and base catalysis. For example, Schumann et al. (77) used a two-stage procedure to speed up entrapment of air-sensitive rhodium complexes. The procedure involved acid hydrolysis to form an initial sol, which was doped with metal complex, and base was added to induce condensation. The effect of this two-step procedure on gel structure was not examined The rhodium complex was effectively trapped within the silicate matrix, however, and was an active catalyst for hydrogenation of styrene and nitrobenzene. [Pg.350]

Notes and discussion. This method allows efficient entry to 4-0-(4-0-acetyl-3,6-di-(9-allyl-2-0-benzyl-P-D-mannopyranosyl)-l,6-anhydro-2-azido-3-0-benzyl-2-deoxy-P-D-glucopranose by use of the silver silicate catalyst procedure. The target is of use for entry to a branched p-mannose containing pentasaccharide, present within A-gly coproteins. [Pg.244]

One of the CVD methods that has been developed is the synthesis of vertically aligned nanofiber bundles for specific applications. The synthesis of VACNF arrays were all carried out in horizontal reactors [37]. All the reported products by vertical floating catalyst method were randomly arranged CNFs. There are few reports on aligned CNF bundles synthesized by floating catalyst procedure in vertical reactors [38]. [Pg.70]

Here are some examples of fabrication of silica xerogel monoliths by one- and two-step catalyst procedures. [Pg.327]

Fabrication procedures of silica monoliths by a one-step catalyst procedure are presented in Ref [20]. A basic procedure to prepare a silica xerogel monolith is by following the stoichiometry ratio (H2O Si) R = 4, while using a similar molar amount of alcohol as a common solvent for achieving homogeneous solution. In fabrication of sol-gel monoliths, the catalyst used has crucial influence. The common route for preparing silica monoliths is to use a recipe based on a one-step catalyst reaction. [Pg.327]

Product Temp, no. °C Catalyst Procedure Solvent DS Product weight d g... [Pg.140]


See other pages where Catalysts procedures is mentioned: [Pg.295]    [Pg.229]    [Pg.28]    [Pg.56]    [Pg.185]    [Pg.1017]    [Pg.155]    [Pg.144]    [Pg.327]    [Pg.328]    [Pg.95]   
See also in sourсe #XX -- [ Pg.300 ]




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