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Racemization comparisons between

Table I. Comparisons between Aspartic Acid Racemization and... Table I. Comparisons between Aspartic Acid Racemization and...
Figure 11.29 Comparison between calculated and experimental band profiles of the racemic mixture of Troger s base on a Chi-ralpak AD coliunn. Sample sizes 3.6, 7.25, 10.85 and 14.5 mg. Solid line - experimental data, dotted line - simulation with three-layer isotherm model, and dashed line -simulation with cooperative and S-shaped isotherm model Reprinted from K. Mihlbach-ler, K. Kaczmarski, A. Seidel-Morgenstem. G. Guiochon, J. Chromatogr. A, 955 (2002) 35 (Fig. 11). Figure 11.29 Comparison between calculated and experimental band profiles of the racemic mixture of Troger s base on a Chi-ralpak AD coliunn. Sample sizes 3.6, 7.25, 10.85 and 14.5 mg. Solid line - experimental data, dotted line - simulation with three-layer isotherm model, and dashed line -simulation with cooperative and S-shaped isotherm model Reprinted from K. Mihlbach-ler, K. Kaczmarski, A. Seidel-Morgenstem. G. Guiochon, J. Chromatogr. A, 955 (2002) 35 (Fig. 11).
As an example for the efficiency of the NN method, Schlinge et al. (2011) published a comparison between simulated and measured chromatograms for a racemic mixture. The NN were validated for a column of 4 x 300 mm and a flow rate of... [Pg.400]

Sceletium Alkaloids.—Full details of an earlier briefly reported synthesis of ( )-mesembrine (3) have been published and a new synthesis has been described. The latter is outlined in Scheme 1 A new Sceletium alkaloid has been isolated from S. namaquense. It has been formulated as (4) on spectral evidence, the assignment of structure being confirmed by direct spectral comparison between the natural base and racemic (4), synthesized earlier. Channaine, another alkaloid of this family, from S. tortuosum, has structure (5) on the basis of an X-ray diffraction analysis of its hexahydrate. It may be an artefact arising from the condensation of a pair of iV-desmethylmesembrenone molecules (6) during isolation. ... [Pg.31]

Fig. lla-d. Comparison between crystals of glycine grown in the absence and presence of additives a pure b (S) additive c (R) additive d racemic additive... [Pg.260]

It has been observed that a 1 1 mixture of pure PLLA with pure PDLA yields a stereocomplex of the two polymers during crystallization or polymerization. The PLA stereocomplex consists of racemic crystalline strucmres in which l-PLA and d-PLA chains are packed side by side, with a 1 1 ratio of l d monomer units [4, 32, 33]. While the melting temperature of a- and P-crystalline forms of PLA falls in the range 170-180°C, the 7) of PLA stereocomplex is between 220 and 230°C [33]. The high of PLLA/PDLA stereocomplex makes it a difficult material for processing however, it is interesting to note that the comparison between PLLA/PDLA equimolar blends and the starting materials shows mechanical properties that are markedly improved. [Pg.148]

Brahmachari, G., and Banerjee, B. (2012). A comparison between catalyst-free and Zr0Cl2.8H20-catalyzed Strecker reactions for the rapid and solvent-free one-pot synthesis of racemic a-aminonitrile derivatives. Asian J. Org. Chem., 1, 521-528. [Pg.76]

Chirality as a Tool - Comparisons between Optically Pure and Racemic Celators and Optically Pure and Racemic Liquids... [Pg.17]

A comparison between retention and resolution factors of commercial and noncommercial plates of acetylated cellulose using ethanol/water (80 20, v/v) as mobile phase was performed by Lepri et al. [12] in 1994. Results of this study are reported in Table 4.2. Ready-to-use cellulose triacetate plates with 20% acetylation degree (AC-20) and 40% acetylation degree (AC-40) showed a different behavior during the development process. In fact, AC-40 plates swelled strongly and stationary phase broke away from the glass support and could not be used. On the contfary, AC-20 plates did not show this inconvenience, but their use was limited to the resolution of four racemates, such as l,l -binaphthyl-2,2 -diamine. [Pg.67]

For a number of the systems, comparisons were made between the effects of enantiomeric composition in the monolayer and corresponding melting-point-composition curves for the crystals. All of the latter gave clear evidence of racemic compound formation in the crystals, and this type of pattern was repeated in the monolayer properties. [Pg.134]


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