Acceptor component

When 3-butyne-2-one 7 is used as a Michael acceptor component, a 2,5-cyclohexadienone, e.g. 8, is obtained as the annulation product ... 

The mixed Claisen condensation of two different esters is similar to the mixed aldol condensation of two different aldehydes or ketones (Section 23.5). Mixed Claisen reactions are successful only when one of the two ester components has no a hydrogens and thus can t form an enolate ion. For example, ethyl benzoate and ethyl formate can t form enolate ions and thus can t serve as donors. They can, however, act as the electrophilic acceptor components in reactions with other ester anions to give mixed /3-keto ester products. 

The Michael reaction occurs with a variety of a,/3-unsaturated carbonyl compounds, not just conjugated ketones. Unsaturated aldehydes, esters, thio-esters, nitriles, amides, and nitro compounds can all act as the electrophilic acceptor component in Michael reactions (Table 23.1). Similarly, a variety of different donors can be used, including /3-diketones, /3-keto esters, malonic esters, /3-keto nitriles, and nitro compounds. 

The 2-keto-3-deoxy-aldonic acid (phosphate) aldolases from Pseudomonas strains - 3-deoxy-2-keto-L-arabonate (F.C 4.1.2.18), 3-deoxy-2-keto-D-xylonate (EC 4.1.2.28), 3-deoxy-2-keto-6-phospho-D-gluconate (EC 4.1.2.14) and 3-deoxy-2-keto-6-phospho-D-galactonate aldolase (EC 4.1.2.21) - appear to be specific even for the acceptor components, but allow stereoselective syntheses of the respective natural substrates29. 

Typically, lyases are quite specific for the nucleophilic donor component owing to mechanistic requirements. Usually, approach of the aldol acceptor to the enzyme-bound nucleophile occurs stereospedfically following an overall retention mechanism, while the facial differentiation of the aldehyde carbonyl is responsible for the relative stereoselectivity. In this manner, the stereochemistry of the C—C bond formation is completely controlled by the enzymes, in general irrespective of the constitution or configuration of the substrate, which renders the enzymes highly predictable. On the other hand, most of the lyases allow a reasonably broad variation of the electrophilic acceptor component that is usually an aldehyde. This feature... 

Using (31) as the nucleophile, FSA has been shown to accept several aldehydes as acceptor components for preparative synthesis [91]. In addition to (31), it also utilizes hydroxyacetone as an alternative donor to generate 1-deoxysugars such as (66) regioselectively (Figure 10.25). 

The sweetness-eliciting units, AH (a proton donor) and B (a proton acceptor) components were respectively assigned to the anomeric OH group on C-2 and the OH group on C-1, and the CH2 group of C-6 was ascribed to a third (hydrophobic) component (X). 

With the aid of a normal coordinate analysis involving different isotopomers a linear structure of the Pd-Si-0 molecule is deduced. The results of ab initio MP2 calculations (Tab. 4) confirm the experimentally obtained IR spectra and their interpretation. The Pd-C bond in PdCO is similar to the Pd-Si bond in PdSiO which means, that the donor bond is strengthened by x acceptor components. This conclusion is in line with the high value of the Pd-Si force constant (exp. f(PdSi) = 2.69, f(SiO) = 8.92 mdyn/A) as well as with the energy of PdSiO (Pd + SiO —> PdSiO + 182 kJ/mol for comparison Pd + CO —> PdCO + 162 kJ/mol, MP2 level of theory). 

Di(ethynyl)gold moieties can be used as bridging units between transition metals as demonstrated for square-grid complexes with Pt(dppe) acceptor components.96... 

Alvaro, M., Ferrer, B., Fornes, V., Garcia, H. and Scaiano, J.C. (2002). Bipyridinium macroring encapsulated within zeolite Y supercages. Preparation and intrazeolitic photochemistry of a common electron acceptor component of rotaxanes and catenanes. J. Phys. Chem. B 106, 6815-6820... 

In the case of weak interactions, which do not always lead to a stoichiometric complex, it is also possible to study the effect of the aromatic substances on the acceptor components, e.g. the solvent itself. 

There is a rule that donor and acceptor components for a planned ion-radical salt should have more or less symmetrical molecular geometry. However, if substituents are not so bulky, they can be located unsymmetrically without detriment to conductivity (Tatemitsu et al. 1985). Scheme 8.11 also testifies that such a rule should be understood dialectically. 

As an interesting challenge we examined an extension of this procedure to its vinylogous analogue [71]. Commonly, reactions between extended dienolates such as 90 and carbonyl compounds have focused on the use of aldehydes as an acceptor component. In contrast, we decided to investigate catalytic asymmetric... 

Contrary to anomalously distant reacting double bonds, the mixed crystal of 1 1 donor-acceptor type cinnamic acids has been reported to be photostable, in which double bonds of adjacent donor and acceptor components in the stack are within photoreactive distance of each other (3.80 A) (14). 

The pH of a bicarbonate buffer system depends on the concentration of H2C03 and I I(X)3, the proton donor and acceptor components. The concentration of H2C03 in turn depends on the concentration of dissolved C02, which in turn depends on the concentration of C02 in the gas phase, called the partial pressure of C02. Thus the pH of a bicarbonate buffer exposed to a gas phase is ultimately determined by the concentration of HC03 in the aqueous phase and the partial pressure of C02 in the gas phase (Box 2 4). 

Functionally and mechanistically reminiscent of the pyruvate lyases, the 2-deoxy-D-ribose 5-phosphate (121) aldolase (RibA EC 4.1.2.4) [363] is involved in the deoxynucleotide metabolism where it catalyzes the addition of acetaldehyde (122) to D-glyceraldehyde 3-phosphate (12) via the transient formation of a lysine Schiff base intermediate (class I). Hence, it is a unique aldolase in that it uses two aldehydic substrates both as the aldol donor and acceptor components. RibA enzymes from several microbial and animal sources have been purified [363-365], and those from Lactobacillus plantarum and E. coli could be induced to crystallization [365-367]. In addition, the E. coli RibA has been cloned [368] and overexpressed. It has a usefully high specific activity [369] of 58 Umg-1 and high affinity for acetaldehyde as the natural aldol donor component (Km = 1.7 mM) [370]. The equilibrium constant for the formation of 121 of 2 x 10M does not strongly favor synthesis. Interestingly, the enzyme s relaxed acceptor specificity allows for substitution of both cosubstrates propional-dehyde 111, acetone 123, or fluoroacetone 124 can replace 122 as the donor [370,371], and a number of aldehydes up to a chain length of 4 non-hydrogen atoms are tolerated as the acceptor moiety (Table 6). 

The transaldolase (EC 2.2.1.2) is an ubiquitous enzyme that is involved in the pentose phosphate pathway of carbohydrate metabolism. The class I lyase, which has been cloned from human [382] and microbial sources [383], transfers a dihydroxyacetone unit between several phosphorylated metabolites. Although yeast transaldolase is commercially available and several unphosphorylated aldehydes have been shown to be able to replace the acceptor component, preparative utilization has mostly been limited to microscale studies [384,385] because of the high enzyme costs and because of the fact that the equilibria usually are close to unity. Also, the stereochemistry of transaldolase products (e.g. 38, 40) [386] matches that of the products from the FruA-type DHAP aldolase which are more effortlessly obtained. 

Electron donors and acceptors for reversible redox systems must invariably exhibit at least two stable oxidation states, or the net result will be an irreversible chemical reaction. The donor or acceptor components of the redox system need not be confined to independent atoms, ions, or molecules but could even be imperfections in crystal lattices capable of functioning as electron traps. The well-known color centers in alkali halides are just such acceptor systems. 

In addition photoexcitation can also result in the transfer of an excited state electron to a distant acceptor group resulting in charge separation. This process can be understood within the framework of Marcus theory and subsequent more sophisticated theoretical treatments.2,5 The rate of electron transfer (ke]) drops with distance according to an attenuation factor / el ke °c exp(—/ el /yB) where /Xb is the distance between donor and acceptor components A and B. When the donor and acceptor components are separated by a vacuum J3el is estimated to be ca. 2-5 A-1. However when some kind of material substance is involved such as a bridge L the electron transfer process can be... 

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