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  • Physical Chemistry  (3)
  • Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry  (2)
  • Wiley-Blackwell  (5)
  • American Institute of Physics
  • National Academy of Sciences
  • Springer Science + Business Media
  • 2020-2022
  • 1990-1994  (5)
Collection
Publisher
  • Wiley-Blackwell  (5)
  • American Institute of Physics
  • National Academy of Sciences
  • Springer Science + Business Media
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Journal of Physical Organic Chemistry 3 (1990), S. 470-476 
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Ab initio theoretical calculations were carried out on the three tautomers, NH, OH and CH, of 1,2,6-thiadiazine 1,1-dioxides. Different basis sets were employed in order to obtain an adequate description of these cyclic sulphamide derivatives. A coherent picture is obtained which includes relative stability of tautomers (NH 〉 CH 〉 OH), non-planarity of NH and CH tautomers and electronic distribution (Boys' localized orbitals).
    Additional Material: 3 Ill.
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  • 2
    ISSN: 0894-3230
    Keywords: Organic Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: The reaction of monosilylated imines and a disilylated enamine with nitrosyl salts in dichloromethane at -78°C is shown to proceed via intermediate vinyl diazonium salts and vinyl cations.
    Additional Material: 1 Tab.
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Archives of Insect Biochemistry and Physiology 17 (1991), S. 143-155 
    ISSN: 0739-4462
    Keywords: reproduction ; vitellin ; Hymenoptera ; caste ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: Vitellogenin has been identified in the ant Camponotus festinatus, both in queens and workers. In the workers, it is already present before adult eclosion in low concentrations (〈1 μg/μl hemolymph). Vitellogenin and vitellin are immunologically identical and are composed of a single type of apoprotein with an apparent Mr = 185,000. The molecular weight of the native molecules was estimated as ∼460,000 by pore limiting gradient electrophoresis. Vitellogenin was detected as a major protein in the hemolymph of young workers, both under queenright and queenless conditions. Thus, in spite of their sterility in the presence of the queen, C. festinatus workers are able to synthetize vitellogenin which is identical both in size and immunologically to the queen vitellogenin. About 6-7 weeks after adult eclosion, however, vitellogenin was usually undetectable in the hemolymph of queenright workers, particularly the minor workers, while it constituted about 30% of total protein in queenless workers. Protein concentration in the hemolymph of queenless insects increased up to 20-fold as compared to 1-day-old insects. Queenless workers also developed large amounts of perivisceral fat body, while queenright workers, particularly the minor workers, showed a dramatic fat body regression about 6 weeks after emergence.
    Additional Material: 7 Ill.
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  • 4
    ISSN: 0739-4462
    Keywords: Bacillus thuringiensis ; Phthorimaea operculella ; insecticidal crystal protein ; receptors ; Chemistry ; Food Science, Agricultural, Medicinal and Pharmaceutical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology
    Notes: The potato tuber moth is susceptible to at least three insecticidal crystal proteins (ICPs) from Bacillus thuringiensis: CrylA(b), CrylB, and CrylC. To design useful combinations of toxin genes either in transgenic plants or in new genetically modified B. thuringiensis strains, it is necessary to determine the binding characteristics of the different ICPs so as not to combine a pair sharing the same binding site. This has been accomplished using two different techniques: 125I-labeling of the ICPs with further measurement of the radioactivity bound to brush border membrane vesicles, and microscopic visualization of the bound ICPs by enzyme-linked reagents such as antibodies or streptavidin using biotinylated ICPs. Our results show that CrylA(b), CrylB, and CrylC bind to different sites in the brush border membrane of midgut epithelial cells. Also, the affinity of the binding sites for the ICPs and their concentration in brush border membrane vesicles has been determined in a laboratory strain and a storage collected population. No significant differences were found between these two strains. © 1994 Wiley-Liss, Inc.
    Additional Material: 3 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Chemical Kinetics 22 (1990), S. 1127-1136 
    ISSN: 0538-8066
    Keywords: Chemistry ; Physical Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The pyrolyses of p-nitrophenyl t-butyl ether, p-methoxyphenyl t-butyl ether, p-aminophenyl t-butyl ether, p-nitrophenyl t-butyl sulfide, and propargyl t-butyl sulfide have been studied in a stirred-flow reactor over the temperature range 430-530°C and pressures in the range 7-14 torr, using toluene as carrier gas. The reactions yielded between 90 and 99% isobutene plus the corresponding phenol, thiophenol, or thiol as products. The first order rate coefficients for reactant consumption, based on isobutene production, followed the Arrhenius equationsp-nitrophenyl t-butyl ether\documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm s}^{ - 1}) = 10^{12.79 \pm 0.24} {\rm exp}(- 179 \pm 3{\rm kJ/mol}RT) $$\end{document} p-methoxyphenyl t-butyl ether \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm s}^{ - 1}) = 10^{14.50 \pm 0.30} {\rm exp}(- 210 \pm 4{\rm kJ/mol}RT) $$\end{document} p-aminophenyl t-butyl ether: \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm s}^{ - 1}) = 10^{14.59 \pm 0.28} {\rm exp}(- 208 \pm 4{\rm kJ/mol}RT) $$\end{document} p-nitrophenyl t-butyl sulfide \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm s}^{ - 1}) = 10^{12.12 \pm 0.27} {\rm exp}(- 185 \pm 4{\rm kJ/mol}RT) $$\end{document} propargyl t--butyl sulfide: \documentclass{article}\pagestyle{empty}\begin{document}$$ k({\rm s}^{ - 1}) = 10^{13.79 \pm 0.24} {\rm exp}(- 204 \pm 3{\rm kJ/mol}RT) $$\end{document}The results support a unimolecular elimination of the isobutene involving polar, four-center cyclic transition states.
    Additional Material: 1 Ill.
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