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Hydrolysis l-

The reaction of 3-benzoxepin with methyllithium results in the addition of two equivalents of the organometallic reagent and cleavage of the heterocycle. After hydrolysis l-[2-(Z)-prop-l-enyl)phenyl]propan-2-ol can be isolated, but no experimental data is available.216 Occasionally, a small amount of the tran.v-isomcr is obtained (less than 10% of the product).12... [Pg.47]

For monitoring the extent of polysaccharide hydrolysis, l.c. methods that sepeu ate and analyze the non-fermentable oligosaccharides (d.p. 3-30) derived from cellulose, hemicellulose, and pectins are useful, and have already been described (see Section III,l,c). For determination of the monosaccharide composition of completely hydrolyzed, plant polysaccharides, l.c. is especially useful and has been applied to the compositional analysis of hydrolyzed plant fiber,wood pulps,plant cell-walls,and cotton fibers.In these representative examples, the major sugars of interest, namely, glucose, xylose, galactose, arabinose, and mannose, have traditionally been difficult to resolve by l.c. The separa-... [Pg.52]

The nitrile produced in the above reaction can be converted into the corresponding carboxylic acid by acid hydrolysis, l.e. reaction with water catalysed by hydrogen ions from the acid. [Pg.58]

Nucleophilic substitution on cyclic sulfates 3 with tetramethylammonium fluoride gives 1,2-fluoro sulfates which can be hydrolyzed to l-fluoro-2-hydroxy derivatives.189 Thus propane-1,2-cyclic sulfate 3 affords after hydrolysis l-fluoro-2-hydroxypropane (4). [Pg.587]

The first report of a distinct effect of silicon on a neighbouring carbenium ion was published as early as 1946. Sommer, Whitmore and coworkers34 35 reported that under conditions of basic hydrolysis, (l-chloroethyl)trichlorosilane 58 and (1-chloropropyl)trichlorosilane 59 failed to give cleavage of the a-C—Cl bond, while under the same conditions the analogous 2-chloroethyl 60 and 2-chloropropyl compounds 61 hydrolyse rapidly. [Pg.610]

In the following, some applications are summarized (Scheme 31). 1-trimethyl-siloxy-bicyclo[4.1.0]-heptane (218) gives after hydrolysis l-hydroxy-bicyclo[4.1.0]-heptane (25J)151, ls2> but further treatment with potassium t-butanolate/ether... [Pg.54]

Acid hydrolysis of cytidine ribitol pyrophosphate led to a series of products, depending on the conditions of hydrolysis. L-Ribitol 1-phosphate (n-ribitol 5-phosphate), isomeric ribitol phosphates formed by acid-catalyzed migration of the phosphate group from the terminal position, and 1,4-anhydro-DL-ribitol were isolated. [Pg.215]

Azaindoles are more stable to air oxidation than indoles, are stable to mild reagents like silver oxide and selenium dioxide, but are readily attacked by permanganate. In the structure proof of 7-aza-indole, Kruber oxidized the 1-benzenesulfonyl derivative with potassium permanganate in acetone solution to obtain 2-(benzene-sulfonyl)aminonicotinic acid. The 1-acetyl and 1-benzoyl derivatives gave inconsistent results, which Kruber attributed to their ease of hydrolysis. l-Benzoyl-2,5-dimethyl-4-azaindole and its 3-substituted derivatives give 3-benzamido-6-methylpicolinic acid with permanganate oxidation. ... [Pg.60]

Hydrolysis L, = 40.0 d was estimated at pH 7 from ethyl chloride data in water at an unspecified temperature (Brown et al. 1975 quoted, Howard 1989) ... [Pg.69]

Hydrolysis first-order hydrolysis L, = 23000 h, based on losses in dark control tests during photolysis experiments (Draper Crosby 1983 quoted, Howard et al. 1991). [Pg.469]

The stability of the hydrolysis species may also be expressed in terms of the hydroxo corriplex formation (cf. Table 6.2, where in case of hydrolysis L = OH" and HL = H2O). [Pg.260]

D- and L-Amino acids (miscellaneous) by amino acid amide hydrolysis L-specific amidase... [Pg.26]

Dichlorocyclopropanes prepared from acetals of a,) -unsaturated alehydes are particularly useful intermediates since they alford, after hydrolysis, l,l-dichloro-2-formylcyclopropanes, which are not readily available by other routes (Table 15). [Pg.652]

Thus, 395 gives via pyrolysis 2,4,6-tris(trimethylsiloxy)-3-pyridinecarbonitrile (J9P) and subsequent hydrolysis 2,4,6-trioxo-3-piperidine carbonitrile (400) whereas direct hydrolysis of395 leads to 2,4,6-trioxopiperidinecarboxamide (397). Analogously,. 96 affords by direct hydrolysis l-methyl-2,4,6-trioxo-3-piperidine[N-methylcar-boxamide] (595),... [Pg.67]

When dialkyl alanes are used in place of trialkyl alanes, the result is generally a mixture of alcohols, with R partly replaced by H. In certain special instances triisobutylalane, for example, reacts with epoxides and H2 or RH is split off. 1,2-Epoxycyclododecane and l,2-epoxycyclodeca-5,9-diene give, after hydrolysis, l-hydroxycyclododeca-2-en (125) and 1-hydroxy-cyclododeca-2,5,9-triene (125) ... [Pg.336]

Polysaccharides.—This research is centered around 1900. Many pectins were isolated from various plants gentian, red currant, and Rosa canina. Bourquelot and H issey were among the first to point out that natural macromolecules, while possessing certain general properties in common, differ nevertheless from one species to another in their degree of complexity. Plant pectins could be differentiated from one another by optical rotation, but all produced, on hydrolysis, L-arabinose and n-galac-tose. [Pg.6]

Lipases. 17,133-134 18, 202-204 Hydrolysis. l,l,l-Trifluoro-2-a the corresponding chloroacetates. aid alkanols have also been successfully 1 is shown in the resolution of menthy group is retained." Selective hydrolys a chiral diol, which has been used iS)-chromanethanol, which is an i 6-acetoxymethyldihydropyran is reso (PPL). These can be used to 2,2 -bis(phenylthiomethyl)dihydropy for 1,2-diols."... [Pg.184]

C,6H 407, Mr 318.28, needles, mp. 184°C (decomp.). A depside from numerous lichens, especially Parme-liaceae and Roccellaceae. L. was synthesized for the first time by E. Fischer in 1913. On acidic hydrolysis L. furnishes orsellinic acid, while alkaline hydrolysis gives orcinol. [Pg.352]


See other pages where Hydrolysis l- is mentioned: [Pg.91]    [Pg.262]    [Pg.449]    [Pg.51]    [Pg.332]    [Pg.16]    [Pg.20]    [Pg.91]    [Pg.289]    [Pg.452]    [Pg.92]    [Pg.296]    [Pg.68]    [Pg.1233]    [Pg.888]    [Pg.640]    [Pg.156]    [Pg.699]    [Pg.898]    [Pg.114]    [Pg.1404]    [Pg.245]    [Pg.687]    [Pg.389]    [Pg.168]    [Pg.223]    [Pg.35]    [Pg.252]    [Pg.64]   
See also in sourсe #XX -- [ Pg.17 , Pg.70 ]




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Hydrolysis of Metal Ions, First Edition. Paul L. Brown and Christian Ekberg

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