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  • Organic Chemistry  (27)
  • biological control  (5)
  • kairomone  (2)
  • General Chemistry
  • 1980-1984  (11)
  • 1975-1979  (18)
  • 1910-1914  (3)
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Year
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 7 (1981), S. 909-917 
    ISSN: 1573-1561
    Keywords: Trichogramma pretiosum ; Hymenoptera ; Trichogrammatidae ; biological control ; kairomone ; Heliothis zea ; Lepidoptera ; Noctuidae ; host density
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Trichogramma pretiosum Riley females exhibit success-motivated searching after oviposition. The stimulatory effect of contact with host eggs makes host-egg density an important factor in determining the appropriate strategy for behavioral manipulation, using kairomones, that simulate host seeking, in biological control programs. Host eggs can be used, in conjunction with kairomones or by themselves, to improve the performance of these important beneficial insects.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-1561
    Keywords: kairomones ; Trichogramma achaeae ; Trichogramma pretiosum ; Microplitis croceipes ; Heliothis Spp. ; host-seeking stimuli ; insect behavior ; releasers ; pest management ; biological control
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Frass from larvae of the corn earworm,Heliothis zea (Boddie) and scales fromH. zea moths (that are known to contain the host-seeking stimulus, tricosane) stimulate and orient host-seeking activity in femaleMicroplitis croceipes (Cresson), a larval parasite ofH. zea, andTrichogramma spp., egg parasites ofH. zea. When larval frass, moth scales, and tricosane were used as sign stimuli (releasers) forM. croceipes, T. pretiosum (Riley), andT. achaeae Nagaraji and Nagarkatti, respectively, at time of their release from laboratory containers, parasite performance improved, resulting in significantly increased rates of parasitization over that of unstimulated parasites. Stimulation ofM. croceipes with larval frass had an overriding effect on this parasite's innate tendency to disperse upon release, thereby increasing the numbers remaining and prolonging their retention in the target area. Supplying the appropriate host-seeking stimuli to these 3 hymenopterous parasites ofH. zea at time of their release to improve their efficiency greatly increases the probability of their effective utilization in pest management systems.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-1561
    Keywords: Trichogramma achaeae ; Heliothis zea ; biological control ; kairomones ; pest management ; parasitoids ; host finding ; insect behavior ; pheromones ; behavior chemicals
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract When the effect of the kairomone, tricosane, on parasitization byTrichogramma achaeae Nagaraja and Nagarkatti of eggs ofHeliothis zea (Boddie) was studied in petri dish tests, the greatest percentage parasitization ( $$\mathop X\limits^\_$$ = 64%) was obtained if the entire filter paper was treated. Treatment of smaller areas (about the eggs) resulted in decreased parasitism. In the greenhouse, highest parasitization ( $$\mathop X\limits^\_$$ = 71%) byT. pretiosum (Riley) ofH. zea eggs placed on pea seedlings grown in pie pans was obtained if the whole pan was treated; lowest parasitism ( $$\mathop X\limits^\_$$ = 29%) occurred when the pans were untreated. Parasitization was intermediate ( $$\mathop X\limits^\_$$ = 52%) in other pans treated only at selected spots. Dissections ofH. zea eggs collected from kairomonetreated and untreated field plots revealed that eggs ofTrichogramma spp. were more efficiently distributed (less superparasitism) among host eggs in treated plots. These kairomones increase parasitization ofTrichogramma spp. by releasing and continuously reinforcing an intensified searching behavior rather than by attracting and guiding the parasite directly to the host.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 5 (1979), S. 673-680 
    ISSN: 1573-1561
    Keywords: Trichogramma ; Hymenoptera ; Trichogrammatidae ; kairomone ; Heliothis zea ; biological control ; pest management ; parasitoids
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract A kairomone from adultHeliothis zea (Boddie) scales is an important factor in the host selection process ofTrichogrammapretiosum Riley. If the host density is sufficiently high (i.e., 1 egg/500 cm2) and higher), a complete coverage or solid treatment of kairomone spray may be the optimum for increasing parasitization rates, but this is not the case at lower host densities (e.g., 1 egg/2000 cm2). At the lower densities, the kairomone must be distributed in such a way as to retain the parasitoids in the target area without inhibiting their movement from one ovi-position site to the next. Simulated moth scale particles appear to fill this need since their density can be regulated to provide the optimum frequency of parasitoid stimulation and thus maximum rates of parasitization at prevailing host densities.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1573-1561
    Keywords: Kairomone ; parasitoids ; biological control ; Trichogramma pretiosum ; Hymenoptera ; Trichogramma tidae ; Heliothis zea ; Lepidoptera ; Noeturidae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract The behavioral response ofTrichogramma pretiosum Riley females to the kairomone found inHeliothis zea (Boddie) moth scales is examined.
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 537-544 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 39. Methane-diphosphonic Esters by U.V.-Induced Michaelis-Becker-ReactionDibromomethane resp. chlorbromomethane reacts with sodium dialkyl phosphite in heptane-/liq.NH3 or in liq. NH3 by u.v. irradiation at low temperatures to give in good yields methane diphosphonic acid tetraalkylesters 1. In the same manner with sodium diethyl thionophosphite the corresponding methane-bis-thiophosphonic acid tetraethylester 4 is obtained.
    Additional Material: 2 Tab.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 324 (1982), S. 545-549 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 40. 1-Trimethylammonium-1-diethylphosphono-1-cyanomethylid, a Stable N-YlidDiethyl-1-dimethylamino-1-cyanomethanephosphonate 4 can be alkylated on nitrogen to the quarternary ammoniumsalts 5, which by C-deprotonation gives the stable N-ylid 8. The N-ylid 8 behaves inert against carbonyl compounds and acylating agents, but can be C-alkylated and  -  involving an ester-dealkylation  -  C-chlorinated.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 320 (1978), S. 389-394 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. XXXI. The Reaction of N,N,N′,N′-Tetramethyl Chloroformamidinium Chloride with P(III) CompoundsN,N,N′,N′-Tetramethyl chloroformamidiniumchloride (4) does not react with triethyl phosphite (TEP) or isopropyl diphenylphosphinate to give the expected bisphosphoryl derivatives 7 and 11, respectively, but primarily the monophosphorylated amidinium salts 6 and 10 respectively. The phosphine oxide 10 is stable, while 6 undergoes an elimination of ethyl chloride to the betain 8. Even under more drastic conditions the reaction of 4 or 8 with TEP does not lead to the expected bis(dimethylamino)bisphosphonate 7, but to the monoaminated bisphosphonate 1, involving a reduction step. Similar reduction has been observed under mild conditions in Michaelis-Arbusov reaction of dichloromethylenimonium chloride, yielding the expected trisphosphonate 2 and the bisphosphonate 1 as a by-product.
    Additional Material: 1 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 325 (1983), S. 437-445 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: α-Substituted Phosphonates. 43. Synthesis and Reactivity of 1,2,3,4-Tetrahydroisochinolin-1-phosphonatesN-Alkyl- and N-arylsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonates 1 have been synthesized from the corresponding 3,4-dihydroisochinoliniumbromides 7 and triethyl-phosphite. The N-unsubstituted 1,2,3,4-tetrahydroisochinolin-1-phosphonate 10 is available starting from the 1,2,3,4-tetrahydroisochinolin-1-phosphonic acid by esterification with triethylformate and splitting off the formyl group of the primarily formed N-formyl derivative 14. - N-Quarternated tetrahydroisochinolines 19 and the 1-phosphorylated derivatives 17, respectively react with triethyl-phosphite in an unexpected way by dealkylation and not by splitting off the isochinolinring. - By Horner-synthesis with 1 the 1-aralkylidene-isochinolines 23 are available in moderate yields.
    Additional Material: 4 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 939-950 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Synthesis and Reactions of 2-Aryloxy-s-trithianes2-Aryloxy-s-trithianes 4 had been prepared from 1-tosyl-imino-1-SIV-1,3,5-trithiane and phenolates. - By self-condensation of 4 1,5-bis-(trithianyl)-1,3,5-trithiapentane 5 and triphenyl-orthoformate 7 are formed, accompanied by further products, which had been isolated in pure state and identified unambiguously by H-n.m.r. and mass-spectra. In the presence of acids the 2-aryloxy-s-trithianes 4 react with nucleophilic aromatic compounds such as phenoles, N,N-dimethylaniline, pyrrole, indole, and thiophenes to give the C-trithianylated products. With mercaptanes 2-alkylthio-s-trithianes are formed.
    Additional Material: 1 Ill.
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