Enantioselective hydrogenation of α-ketoesters over Pt/alumina modified with cinchonidine: theoretical investigation of the substrate-modifier interaction

Enantio-differentiation in the asymmetric hydrogenation of -ketoesters to -hydroxyesters over platinum catalysts modified with cinchona-alkaloid modifiers occurs through interaction of the ketoester with the cinchona modifier. The structure of the probable transition complex has been calculated for the system methyl pyruvate (substrate) cinchonidine (modifier) using molecular mechanics and quantum chemistry techniques at both ab initio and semiempirical levels. The calculations suggest that protonated cinchonidine is energetically more likely to interact with the substrate and that the crucial interaction occurs via hydrogen bonding of the quinuclidine nitrogen and the oxygen of the -carbonyl moiety of methyl pyruvate. In this complex the methyl pyruvate is transformed into a half-hydrogenated species which is adsorbed on the platinum surface and on hydrogenation yields the product methyll actate. Theoretical studies indicate that adsorption of the complex leading to (R) -methyl lactate is energetically more favourable than that of the corresponding complex which yields (S) -methyl lactate, which may be the key for the enantio-differentiation.     

Synthesis and properties of aromatic polyesters and brominated polyesters derived from α,α′-bis(4-hydroxyphenyl)-1,4(or 1,3)-diisopropylbenzene

The interfacial polycondensation technique was used for the preparation of polyarylates and brominated polyarylates. Polyarylates and brominated polyarylates were prepared by mixing a solution of diacid chloride such as terephthaloyl chloride, isophthaloyl chloride, or their mixture in dichloromethane with an aqueous alkaline solution of ,-bis(4-hydroxyphenyl)-1,4(or 1,3)-diisopropylbenzene or ,-bis(4-hydroxy-3,5-dibromophenyl)-1,4(or 1,3)-diisopropylbenzene using triethylbenzylammonium chloride as the phase transfer agent. Moderate to high molecular weight polyarylates with _inh up to 1.27 dL/g were obtained, and most of them could be cast into tough and flexible films depending on the polymer composition. In general, polymers containing more 1,3-isomer or isophthaloyl chloride moieties gave transparent and flexible films and had lower glass transition temperatures and higher solubility. Although these polymers have two isopropylidene linkages in their repeating units, they still exhibit moderately high thermal stability and show no obvious weight loss before 400 °C. The introduction of bromine on the polymer backbone caused a decrease of inherent viscosity, crystallinity, and thermal stability of the polyarylates, while causing an increase in glass transition temperature and a great enhancement of fire retardancy.     

Mechanisms of Iron Activation on Fe-Containing Zeolites and the Charge of α-Oxygen

According to previous Mössbauer data [1] -sites formation at the activation of Fe-containing zeolites is accompanied by irreversible self-reduction of the iron, proceeding without participation of an external reducing agent. Reduced Fe²⁺ ions are inert to O₂ but are reversibly oxidized to Fe³⁺ by N₂O, generating the -oxygen species, O, which provide selective oxidation of hydrocarbons.In this work, the mechanism of -sites formation was studied via quantitative measurement of the dioxygen amount desorbed into the gas phase at the step of self-reduction. A prominent role of the zeolite matrix chemical composition has been revealed. For example, with zeolites of Al–Si composition (FeZSM-5 and Fe-), heating to 900 °C in a closed vacuum space leads to irreversible evolution of O₂, which is accompanied by the immediate formation of -sites. Similar heating of B–Si and Ti–Si zeolites also leads to dioxygen evolution; however, this evolution is reversible and is not accompanied by formation of -sites. Activation of these zeolites occurs only in the presence of water vapor. Stoichiometric measurements showed that in terms of charge one regular O^2- ion, removed at the activation, is equivalent to two -oxygen atoms. So, -oxygen is identified as an ion-radical species O ^-., whose unique oxidation properties still distinguish it from the generally observed O^-. radicals.The mechanism of -sites formation is proposed, in which the process of strong chemical stabilization of reduced Fe²⁺ atoms in the zeolite structure is a key step, making impossible the reoxidation of the iron with O₂.     

Isolation of the diterpenoids, ent-kauran-16alpha-ol and ent-atisan-16alpha-ol, from sunflowers, as oviposition stimulants for the banded sunflower moth, Cochylis hospes

Two diterpenoid alcohols, ent-kauran-16-ol (1) and ent-atisan-16-ol (2), were isolated from pre bloom (R3-R4 stage) sunflower heads as oviposition stimulants for the banded sunflower moth, Cochylis hospes. Fractionation of a sunflower head extract, by normal-phase flash column chromatography, resulted in an early eluting fraction exhibiting significant activity in an egg-laying bioassay. Compounds 1 and 2, along with ent-trachyloban- 19-oic acid (3) and ent-kaur-16-en-19-oic acid (4), were isolated as the major components of this fraction and identified by their NMR and mass spectra. The purified compounds were individually tested for ovipositional activity in dose-response bioassays. In these bioassays, compounds 1 and 2 gave linear dose responses, with increasing numbers of eggs laid as the dosage of either increased. Compounds 3 and 4 failed to stimulate significant egg-laying at any of the dosages tested. A factorial design bioassay, using compounds 1 and 2, showed that 1 was relatively more stimulatory than 2, and that there was no synergistic effect on oviposition when the two compounds were combined.     

Highly Efficient Platinum-Catalyzed Enantioselective Hydrogenation of Trifluoroacetoacetates in Acidic Solvents

The hydrogenation of methyl-, ethyl- and isopropyl-4,4,4-trifluoroacetoacetates to the corresponding chiral trifluoromethyl alcohols has been investigated over Pt/A1₂O₃ modified by O-methyl-cinchonidine. Up to 96% ee and 1850 h^-1 average TOF have been achieved in the synthesis of this important chiral building block. The special role of reaction medium and particularly the impact of water and acids on enantiodiscrimination are discussed.     

Surface properties of ZSM-5 modified by phosphorus

Phosphorus modification of ZSM-5 leads to extra framework P⁵⁺ and probably incorporation of +3 valence state of P in the framework. The resulting system has increased Brønsted acidity. Theoretical calculations also favour the postulate that phosphorus in +3 valence state can be incorporated into the lattice.     

Response of the European elm bark beetle,Scolytus multistriatus (Coleoptera: Scolytidae), to isomers and components of its pheromone

Laboratory bioassays (two methods) and field tests demonstrated synergistic action of the three components [(–)-4-methyl-3-heptanol (I); (–)-2,4-dimethyl-5-ethyl-6,8-dioxabicylo[3.2.1]octane (-multistriatin) (II); and (–)--cubebene (III)] of the pheromone bouquet ofScolytus multistriatus. Individually and in pairs the components were slightly attractive; I+II was clearly the most active doublet. Indirect evidence indicates that only one of the four enantiomers of I is active. Of the , , and isomers of II, only the is active. With the addition of compound I, slightly attractive extract from mated females became nearly as active as extract from virgin females.     

Synergistic interaction between potato glycoalkaloidsα-solanine andα-chaconine in relation to destabilization of cell membranes: Ecological implications

In studies of the lysis of rabbit erythrocytes, red beet cells, andPenicillium notatum protoplasts by the potato glycoalkaloids -solanine and -chaconine, the latter was consistently the more membrane-disruptive compound and erythrocytes the more susceptible cell type. A 11 mixture of solanine and chaconine produced pronounced synergistic effects in all three test systems. In beet cells, such effects were apparent from an early stage of treatment and persisted over a period of several hours. With erythrocytes and fungal protoplasts, the synergism was maximal with mixtures containing approximately 70% chaconine, whereas with beet cells it peaked at approximately 40% chaconine. Synergistic interactions between solanine and chaconine also occurred with regard to cholesterol binding in vitro, with a maximum response corresponding to the 50% mixture. The implications of these findings for the nature and efficacy of chemical defense systems in plants are discussed.     

Structural significance of the alkyl substituent at the C-4 of (+)-trans-verbenyl acetate in sex pheromonal activity of the American cockroach

The significance of the alkyl group at the C-4 of (+)-trans-verbenyl acetate, which is the sex pheromone mimic of the American cockroach, was investigated. Seven alcohols possessing an ethyl, propyl, or dimethyl group at this position of the 6,6-dimethylbicyclo[3.1.1]heptane skeleton were synthesized and evaluated by behavioral assay. All of the alcohols were inactive, while three of four acetates of the 2-alcohols induced sexual behavior in male cockroaches at the 0.02 or 0.5 mg dosage level, either of which is many orders of magnitude higher than the threshold level of the natural sex pheromones (10^–8 mg). Among the acetates, the compounds with a methyl group or an -oriented ethyl group at C-4 showed the highest activity. The results are discussed in terms of spatial requirements of the molecules for interactions with the receptor.Studies on the sex pheromone mimic of the American cockroach, (+)-trans-verbenyl acetate. Part VIII. For Part VII, seeComp. Biochem. Physiol.,70A: 229–234 (1981).     

Factors governing the electrochemical synthesis of α-nickel (ii) hydroxide

The electrodeposition of -nickel hydroxide is promoted by the simultaneous chemical corrosion of the electrode by an acidic nitrate bath. Chemical corrosion results in the formation of a poorly ordered layered phase which is structurally similar to -nickel hydroxide and provides nucleation sites for the deposition of the latter. Therefore under conditions which enhance corrosion rates such as low current density (<1.3 mA cm–2), high temperature (60 C), high nickel nitrate concentration ( 1M) and the resultant low pH (1.7), -nickel hydroxide electrodeposition is observed, while -nickel hydroxide forms under other conditions. Further, -nickel hydroxide deposition is more facile on an iron electrode compared to nickel or platinum.     

Enhancement of the activities with feedstream doping by tetrachloromethane in the oxidative dehydrogenation of propane on α-magnesium pyrovanadate

The oxidative dehydrogenation of propane to propylene has been investigated on -magnesium pyrovanadate (Mg₂V₂O₇) at 723 K in the presence and absence of tetrachloromethane (TCM). Under the present conditions, the conversion of propane and the selectivity to propylene were 5.0 and 74.5%, respectively, in the absence of TCM while those were 14.0 and 70.2%, respectively, upon addition of a small amount of TCM (P(TCM) = 0.34 kPa) into the feedstream on the catalyst. The conversion of propane on Mg₂V₂O₇ without oxidant in the presence and absence of TCM revealed that a contribution of lattice oxygen in the catalyst to the oxidation was strongly controlled by the addition of TCM, resulting in the enhancement of the activity with TCM.     

Apple Fruit Infested with Codling Moth are More Attractive to Neonate Codling Moth Larvae and Possess Increased Amounts of (E,E)-α-Farnesene

Apple fruit artificially infested with codling moth larvae attracted significantly more neonate larvae of the codling moth, Cydia pomonella than uninfested fruit. A greater number of larvae responded to odor in an olfactometer from codling moth-infested cold-stored Red Delicious thinning apples than uninfested apples. Immature Granny Smith, Red Delicious, or Golden Delicious apples that were infested on the tree for five days by codling moth larvae were more attractive to neonate codling moth larvae than similar but uninfested fruit of the same varieties. Apples infested on the tree and sampled five days later also contained significantly greater amounts of the larval attractant (E,E)--farnesene, compared to uninfested apples. Other types of injury to apple fruit did not produce results similar to that from codling moth infestation, either in increased attractiveness to codling moth larvae or in increased quantities of (E,E)--farnesene. These results are consistent with the reported attractiveness of (E,E)--farnesene to neonate codling moth larvae.     

Host-Plant Chemicals and Distribution of Neuquenaphis on Nothofagus

Extractable metabolites from leaves (EM) and volatiles released from six Nothofagus species were analyzed by TLC and GC-MS, respectively. Aphids of the genus Neuquenaphis, closely associated to Nothofagus, were sampled on each Nathofagus species. Cluster analyses of Nothofagus species were performed based on the presence or absence of EM and volatiles. Dissimilarity distances, from the cluster analyses of EM and volatiles, were used to evaluate their association with the aphid distribution. A major component identified from EM and volatiles of three species of Nothofagus, -agarofuran, was attractive to alates of the oligophagous Neuquenaphis sensoriata, which use them as hosts. These results suggest that chemicals play a significant role in the host-plant associations between Neuquenaphis and Nothofagus.     

Isolation and identification of cotton synomones mediating searching behavior by parasitoidCampoletis sonorensis

In laboratory bioassays, the parasitoidCampoletis sonorensis was attracted to the following sesquiterpenes isolated from cotton essential oil: -humulene, -bisabolene, -caryophyllene oxide, spathulenol, -bisabolol, and a new, naturally occurring bisabolene-related alcohol, (2-p-tolyl-6-methylhept-5-en-2-ol) which we name gossonorol. This is the first report of spathulenol in cotton. -Caryophyllene, a major component of cotton, was not attractive to the parasitoids. The response of the parasitoids to these compounds and the possibility of augmenting parasitoid activity in the field by manipulating plant secondary metabolites is discussed.Synomone: A chemical produced or acquired by an organism that benefits both the emitting and receiving organisms (Nordlund and Lewis, 1976).     

Electrosynthesis of 4,4′-dinitroazobenzene on PbO2 electrodes

Parameters which affect the electrosynthesis of 4,4-dinitroazobenzene from p-nitroaniline on platinum and PbO₂ electrodes were investigated and optimum conditions were determined. Maximum conversion efficiency for electrosynthesis was 95% with a pure -PbO₂ electrode. It was found that the electrocatalytic activity of a PbO₂ electrode depends upon its / ratio and its degree of crystallinity. The effects of the added base and water on the conversion efficiency were also elucidated.     

Defensive sesquiterpenoids from a dipterocarp (Dipterocarpus kerrii)

Four sesquiterpenoids (2, 4, 7, and9) have been isolated and characterized from the termiticidal fraction ofDipterocarpus kerrii resin. The major constituent of this resin is -gurjunene (1).Presented at the Third Annual Meeting of the International Society of Chemical Ecology, June 21–24, 1986, University of California, Berkeley.     

Effects of Four Monoterpenes on Germination, Primary Root Growth, and Mitochondrial Respiration of Maize

The effects of four monoterpenes—camphor, eucaliptol, limonene, and -pinene—on the oxidative metabolism of mitochondria isolated from maize root (Zea mays), on maize seed germination, and on primary root growth were investigated. The effects of individual monoterpenes on respiration were variable. -Pinene concentrations of 0.05–1.0 mM stimulated respiration with a mixture of substrates composed of NADH, L-malate, succinate, and L-glutamate, and in the absence of exogenously added ADP (basal respiration). However, at concentrations higher than 1.0 mM, -pinene inhibited respiration both in the absence (basal respiration) and presence of ADP (coupled respiration). Limonene at 0.1 mM or above stimulated basal respiration and inhibited in parallel the coupled respiration. Similar effects were promoted by eucaliptol, but at a higher concentration range (1.0 mM or above). Camphor was less active. At 10 mM concentration, it caused stimulation of basal respiration but did not affect coupled respiration. In the concentration range 0.1–10.0 mM, limonene was inactive on seed germination and primary root growth. Camphor and eucaliptol did not inhibit germination but reduced fresh and/or dry weight of roots at 5.0 mM and above. -Pinene inhibited both seed germination and fresh weight of primary roots at 10.0 mM concentration. The results indicate that intact seeds and primary roots are less sensitive than isolated mitochondria. The relatively more lipophilic monoterpenes -pinene and limonene had less activity than the more water-soluble oxygenated monoterpenes camphor and eucaliptol in inhibiting seed germination and/or primary root growth, despite the fact that they had a higher activity on the oxidative metabolism of isolated mitochondria. The findings suggest that the solubility of monoterpenes may be the major factor implicated in these differences.     

Allelopathic Effects of Volatile Monoterpenoids Produced by <Emphasis Type="Italic">Salvia leucophylla</Emphasis>: Inhibition of Cell Proliferation and DNA Synthesis in the Root Apical Meristem of <Emphasis Type="Italic">Brassica campestris</Emphasis> Seedlings

Salvia leucophylla, a shrub observed in coastal south California, produces several volatile monoterpenoids (camphor, 1,8-cineole, -pinene, -pinene, and camphene) that potentially act as allelochemicals. The effects of these were examined using Brassica campestris as the test plant. Camphor, 1,8-cineole, and -pinene inhibited germination of B. campestris seeds at high concentrations, whereas -pinene and camphene did not. Root growth was inhibited by all five monoterpenoids in a dose-dependent manner, but hypocotyl growth was largely unaffected. The monoterpenoids did not alter the sizes of matured cells in either hypocotyls or roots, indicating that cell expansion is relatively insensitive to these compounds. They did not decrease the mitotic index in the shoot apical region, but specifically lowered mitotic index in the root apical meristem. Moreover, morphological and biochemical analyses on the incorporation of 5-bromo-2-deoxyuridine into DNA demonstrated that the monoterpenoids inhibit both cell-nuclear and organelle DNA synthesis in the root apical meristem. These results suggest that the monoterpenoids produced by S. leucophylla could interfere with the growth of other plants in its vicinity through inhibition of cell proliferation in the root apical meristem.     

Inhibition of Fungal Spore Germination by Nasutitermes: Evidence for a Possible Antiseptic Role of Soldier Defensive Secretions

The antifungal property of two of the principal components of the terpenoid frontal gland secretions of nasute termite soldiers was studied by incubating spore suspensions of the fungus Metarhizium anisopliae with -pinene and limonene singly or in combination at different concentrations. In vitro assays showed that these substances reduced spore germination through direct and indirect (vapor) contact. To determine if the frontal gland secretions protected termites from fungal infection in vivo, the effect of M. anisopliae on the time course of survival of Nasutitermes costalis and N. nigriceps was studied by exposing termites to either a 4.3 × 10⁷ spores/ml or a control sporeless suspension. The caste composition of experimental groups was manipulated to create mixed-caste subcolonies and monocaste groups. Relative to Coptotermes formosanus, a species that relies on the mechanical defenses of soldiers, N. costalis and N. nigriceps were less susceptible to fungal infection. Spore-exposed N. costalis and N. nigriceps termites had 1.2 times the hazard ratio of death of controls, while the hazard ratio of death of spore-exposed C. formosanus was 11.4 times that of controls. Although the lower susceptibility to infection in Nasutitermes may be explained in part by the antifungal properties of -pinene and limonene, group composition also played a major role in the survival of spore-exposed termites. Mixed-caste and soldier monocaste groups had 3.4 and 4.7 times the hazard ratio of death, respectively, relative to the worker monocaste treatment. These results suggest that although Nasutitermes terpenoid secretions may have antifungal properties, the caste composition of groups and the social interactions of termites also play a role in determining susceptibility to fungal infection.     

Kinetics and Mechanism of Copolymerization of α-terpineol with Methylmethacrylate in Presence of Azobisisobutyronitrile as an Initiator

The radical copolymerization of -terpineol with methyl-methacrylate in xylene at 80±0.1C for 50 minutes in the presence of azobisisobutyronitrile (AIBN) follows ideal kinetics and results in the formation of a functional and random copolymer. The activation energy is 33 KJ/mole. The IR spectrum and NMR spectra of the copolymer(s) shows the bands at 1750 and 3400 cm^–1 for ester group of methylmethacrylate and alcoholic group of -terpineol and peaks at 3 to 4 for methoxy group and at 6.5 to 7.5 due to alcoholic group of methylmethacrylate and -terpineol repectively. The values of reactivity ratios, calculated by Kelen–Tüdos method, are r ₁ (MMA) = 0.18 and r ₂ (-terpineol) = 0.046. The Alfrey-Price; Q–e parameters for -terpineol has been calculated as 0.149 and 2.486. The mechanism of copolymerization has been elucidated and it is concluded that the double bond present in the monocyclic ring of -terpineol is an active site for copolymerization and the alcoholic group of -terpineol remain to give functional copolymer.