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CLEAs

Diketene (635) is converted into 3-phenyl-3-butenoic acid (636) by the reaction of phenylzinc, magnesium, and aluminum reagents via C—O bond clea-vage[495j. [Pg.217]

Solution 2-Methyl-3-pentanol, an open-chain alcohol, has M+ = 102 and might be expected to fragment by o- cleavage and by dehydration. These processes would lead to fragment ions of m/z = 84, 73, and 59. Of the three expected fragments, dehydration is not observed (no m/z = 84 peak), but both a clea iges take place (m/z = 73, 59). [Pg.417]

Durrell, Lawrence. The Alexandria Quartet... Justine. Balthazar. Mountolive. Clea. (With revisions.). London Faber, 1962. 884p. [Pg.676]

Immobilized enzymes, particularly LAC, have been employed in the degradation of triclosan. The immobilization of LAC from Coriolopsis polyzona through the formation of cross-linked enzyme aggregates (CLEAs) and their subsequent use in an FBR for the removal of endocrine disrupting compounds [42] produced the complete removal of triclosan, nonylphenol, and bisphenol A (5 mg L-1 each) at a HRT of 150 min. The application of CLEAs in a perfusion basket reactor [43]... [Pg.182]

Enzymatic degradation was tested with commercial LAC from M. thermophila (2,000 U L ). E2 and EE2 were completely degraded even in the absence of mediators after 3 and 5 h, respectively, and after 1 h in the presence of some mediators. For El total removal was achieved in 8 h in the presence of VA and >70% for the other mediators after 24 h, whereas elimination reached 65% in the absence of mediators [8]. The immobilization of this enzyme by encapsulation in a sol-gel matrix [58] was employed for the treatment of a mixture of El, E2, and EE2 both in a batch stirred tank reactor (BSTR) operating in cycles and a continuous PBR. Removal of estrogens was >85% in the BSTR and 55%, 75%, and 60% for El, E2, and EE2, respectively, in the PBR. Both systems were able to reduce the estrogenic activity of the mixture in 63%. Likewise, the immobilization of VP in the form of CLEAs completely removed E2 and EE2 within 10 min from batch experiments, with a concomitant reduction of estrogenic activity, higher than 60% for both compounds [44]. [Pg.186]

VP from B. adust a enzyme Flask scale with CLEAs... [Pg.208]

The iron(III) complexes FeL33+, where L = 2,21-bipyridine and various substituted 1,10-phenanthrolines, cleave a variety of or-ganometals in acetonitrile according to the general reaction mechanism in Scheme I (6). The activation process for oxidative clea-... [Pg.117]

Effective and simple immobilization of enzymes can be obtained by the cross-linking of enzyme aggregates, so-called CLEAs [55]. In this way, essentially any enzyme, including crude preparations, can be transformed into a heterogeneous type of material, insoluble in both water and organic solvents, that is stable and recyclable with high retention of the enzyme s original activity [56], These enzyme preparations are, therefore, of special value for both bio-bio and bio-chemo cascade processes. [Pg.293]

ETHER CLEA VAGE REACTION LEADING TO POLY(ETHER ESTER) RESINS... [Pg.718]

Citrate buffer (0.1 m, pH 2.5, 20 /iL), 3-pyridinecarboxaldehyde (300 mg) and CLEA -immobilized HNL (40 mg) were added to 9.7 mL of the dichloromethane-HCN solution and the reaction was aged for 2-20 h at 5 °C. Commercially available CLEAS of almond HNL (PaHNL-CLEA ) and cassava HNL (MeHNL-CLEA ) were used to catalyze the syntheses of R)- and (5)-cyanohydrin respectively. [Pg.267]

The use of CLEA preparations of commercially available HNLs allowed for the enantiocomplementary production of cyanohydrins from a pyridinecarboxaldehyde at a much higher chiral purity than had previously been demonstrated with any chemical catalyst. The key to the success of this process was the use of the CLEA -immobilized biocatalysts that allowed reaction conditions to be chosen to minimize the negative effects of the nonspecific background reaction. [Pg.267]

Zalipsky S, et al. New detachable poly(ethylene glycol) conjugates cysteine-clea-vable lipopolymers regenerating natural phospholipid, diacyl phosphatidyletha-nolamine. Bioconj Chem 1999 10 703. [Pg.291]

GEN.257.1. Prigogine, Einstein and Magritte. A study of creativity, Conference, Einstein Meets Magritte, CLEA, VUB, mai 1995 public en 1999 in Einstein Meets Magritte, Kluwer, Dordrecht, pp. 99-105. [Pg.79]

Both acylation and deacylation can be performed with a lipase as shown in Scheme 6.9 in which a CALB CLEA was used in the deacylation step that, not surprisingly, was rather slow compared to deacylation with pen acylase. [Pg.117]


See other pages where CLEAs is mentioned: [Pg.351]    [Pg.196]    [Pg.218]    [Pg.368]    [Pg.388]    [Pg.1302]    [Pg.868]    [Pg.583]    [Pg.583]    [Pg.714]    [Pg.397]    [Pg.408]    [Pg.185]    [Pg.112]    [Pg.187]    [Pg.166]    [Pg.183]    [Pg.205]    [Pg.206]    [Pg.206]    [Pg.207]    [Pg.642]    [Pg.297]    [Pg.60]    [Pg.63]    [Pg.80]    [Pg.266]    [Pg.266]    [Pg.266]    [Pg.266]    [Pg.419]    [Pg.95]    [Pg.111]    [Pg.117]   


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CLEA/CLEC

CLEA/CLEC (cross-linked enzyme

CLEAs aggregates

CLEAs and sol-gel HNLs

Combi CLEAs

Cross-linked enzyme aggregates CLEAs)

Immobilization of Enzymes Cross-linked Enzyme Aggregates (CLEAs)

Immobilization techniques CLEAs)

The CLEA Model

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