Ineffective procedures

This procedure provides a practical demonstration of the effectiveness or ineffectiveness of the program. 

Classical reducing agents are known generally to be ineffective in the reduction of sulphones . Thus, although the procedure of Bouveault and Blanc has been used... 

An alternative method of preparing the saturated cyclic amines via cyclopolymerization of diallylamine or diallylammonium chloride was unsuccessful. Common free radical initiators such as 2,2 -azobisisobutyronitrile, ammonium persulfate, benzoyl peroxide were found to be ineffective. Several procedures reported in the literature were followed, and unfortunately all of them have resulted only a small amount of low molecular weight oligomers. Further research for polymerization conditions and types of initiation is still required. 

Selective removal of one isopropylidene group from a diacetal may be achieved by a variety of procedures, most of them involving protic or Lewis acids.100 Particularly common is the hydrolysis of the acetal engaging of the primary position of di-O-isopropylidene derivatives. Bhaskar et al,101 studied the selective deprotection of di-O-isopropylidene acetals derived from D-glucose, D-xylose, and D-mannose, using acid zeolites and montmorillonite K-10. When 102 was submitted to acid hydrolysis in aqueous methanol, the best yields (85—96%) for the monoacetal 105 were obtained when H-beta and HZSM-5 zeolites were employed as catalysts (Scheme 24, Table IV). HY zeolite proved to be ineffective, whereas the yield obtained for the montmorillonite K-10-catalyzed reaction was low (22%). The zeolites found most effective were then used for the hydrolysis of the diacetal 103 and 104, providing excellent yields for the desired corresponding monoacetals 106 and 107. 

Remove excess crosslinker by centrifugal dialysis or gel filtration using a molecular weight exclusion of 5,000. This procedure should be done quickly due to the labile nature of the maleimide group in aqueous solution, which will hydrolyze to a ring-open maleamic acid that is ineffective at coupling to thiols. 

Taylor and Zeitlin [43] described an X-ray fluorescence procedure for the determination of total sulfur in seawater. They studied the matrix effects of sodium chloride, sodium tetraborate, and lithium chloride and show that the X-ray fluorescence of sulfur in seawater experiences an enhancement by chloride and a suppression by sodium that fortuitously almost cancel out. The use of soft scattered radiation as an internal standard is ineffective in compensating for matrix effects but does diminish the effects of instrument variations and sample inhomogeneity. 

A seemingly innocent change in the procedures, e.g. in parts, in staffing, was, almost without exception, the alteration that initiated the propagation and escalation of the deviation. Had the corresponding control loop not been ineffective then the escalation most likely would have been most likely prevented. 

Fires involving alkylaluminium compounds are difficult to control and must be treated appropriately to particular circumstances [1,5,6], usually with dry-powder extinguishers. Halocarbon fire extinguishants (carbon tetrachloride, chloro-bromomethane, etc.), water or water-based foam must not be applied to alkylaluminium fires. Carbon dioxide is ineffective unless dilute solutions are involved [5,6], Suitable handling and disposal procedures have been detailed for both laboratory [1,2,5,6,7] and manufacturing [5,6] scales of operation. 

The application of phase-transfer catalysis to the Williamson synthesis of ethers has been exploited widely and is far superior to any classical method for the synthesis of aliphatic ethers. Probably the first example of the use of a quaternary ammonium salt to promote a nucleophilic substitution reaction is the formation of a benzyl ether using a stoichiometric amount of tetraethylammonium hydroxide [1]. Starks mentions the potential value of the quaternary ammonium catalyst for Williamson synthesis of ethers [2] and its versatility in the synthesis of methyl ethers and other alkyl ethers was soon established [3-5]. The procedure has considerable advantages over the classical Williamson synthesis both in reaction time and yields and is certainly more convenient than the use of diazomethane for the preparation of methyl ethers. Under liquidrliquid two-phase conditions, tertiary and secondary alcohols react less readily than do primary alcohols, and secondary alkyl halides tend to be ineffective. However, reactions which one might expect to be sterically inhibited are successful under phase-transfer catalytic conditions [e.g. 6]. Microwave irradiation and solidrliquid phase-transfer catalytic conditions reduce reaction times considerably [7]. 

Next several methods of filtering the pesticide contaminated wastewater were evaluated. Particle size filters were Ineffective since many of the particles are microcolloidal in size. Likewise coalescer type filters were generally Inadequate. After studying these filtration techniques, flocculation procedures were... 

Rate experiments that are typically carried out in the presence of different concentrations of an alternative product (or product analog) while using the normal substrates . This approach can be particularly useful when the normal product cannot be used because it is unstable, insoluble, or ineffective (the latter indicated by a very high Ki value). Moreover, the normal product may be consumed as an essential substrate in a coupled assay system for the primary enzyme. Fromm and Zewe used the alternative product inhibition approach in their study of hexokinase. Wratten and Cleland later applied this procedure to exclude the Theorell-Chance mechanism for liver alcohol dehydrogenase. See Abortive Complexes... 

A potential limitation encountered when one seeks to characterize the kinetic binding order of certain rapid equilibrium enzyme-catalyzed reactions containing specific abortive complexes. Frieden pointed out that initial rate kinetics alone were limited in the ability to distinguish a rapid equilibrium random Bi Bi mechanism from a rapid equilibrium ordered Bi Bi mechanism if the ordered mechanism could also form the EB and EP abortive complexes. Isotope exchange at equilibrium experiments would also be ineffective. However, such a dilemma would be a problem only for those rapid equilibrium enzymes having fccat values less than 30-50 sec h For those rapid equilibrium systems in which kcat is small, Frieden s dilemma necessitates the use of procedures other than standard initial rate kinetics. 

Since the PSP toxins lack native fluorescence, useful UV absorption or adequate volatility, more traditional analytical procedures such as gas chromatography or spectrometry have proven ineffective in assaying for the toxins. A number of chemical assays for the toxins have been developed though with the fluorometric method of Bates and Rapoport (3 ) proving to be the most useful to date. This assay is based on oxidation of the PSP toxins under alkaline conditions to fluorescent derivatives. The assay is highly sensitive, fairly specific for the PSP toxins and was incorporated into a detection method in the column chromatographic separation of the toxins described by Buckley et al (4 ). 

Microfibrillar collagen hemostat Microfibrillar collagen hemostat is synthesized from cow collagen. It is used for surgical intervention as an adjuvant drug for bleeding when other procedures are ineffective and impractical. A synonym of this drug is avitene. 

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