Search Results - (Author, Cooperation:D. Moiseev)
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1Latest Papers from Table of Contents or Articles in PressH. Pauli ; M. Gottfried ; S. Dullinger ; O. Abdaladze ; M. Akhalkatsi ; J. L. Benito Alonso ; G. Coldea ; J. Dick ; B. Erschbamer ; R. Fernandez Calzado ; D. Ghosn ; J. I. Holten ; R. Kanka ; G. Kazakis ; J. Kollar ; P. Larsson ; P. Moiseev ; D. Moiseev ; U. Molau ; J. Molero Mesa ; L. Nagy ; G. Pelino ; M. Puscas ; G. Rossi ; A. Stanisci ; A. O. Syverhuset ; J. P. Theurillat ; M. Tomaselli ; P. Unterluggauer ; L. Villar ; P. Vittoz ; G. Grabherr
American Association for the Advancement of Science (AAAS)
Published 2012Staff ViewPublication Date: 2012-04-21Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: *Altitude ; *Biodiversity ; Climate ; *Ecosystem ; Europe ; Geological Phenomena ; *PlantsPublished by: -
2Articles: DFG German National LicensesStaff View
ISSN: 1573-8353Keywords: 1′-alkyl-1′,4′-dihydro-2,3′-biquinolyl-4′-thiones ; 1′-alkyl-3-(2-quinolyl)quinolinium halides ; 2,3′-biquinolyls ; nucleophilic substitution ; rearrangement ; thiolationSource: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract Thiolation of 1-alkyl-3-(2-quinolyl)quinolinium halides by a mixture of sulfur with KOH in DMF leads to formation of 1′-alkyl-1′,4′-dihydro-2,3′-biquinolyl-4′-thiones, rearrangement of which in boiling ethylene glycol makes it possible to obtain 4′-alkylthio-2,3′-biquinolyls.Type of Medium: Electronic ResourceURL: -
3Articles: DFG German National LicensesEmel'yanov, I. Ya. ; Grebennikov, R. V. ; Moiseev, D. N. ; Karasev, V. S. ; Kislik, V. S. ; Shved, Yu. F. ; Mel'nik-Kutsyn, Yu. P. ; Lutsenko, N. M. ; Demidov, P. I. ; Sumets, N. G.
Springer
Published 1971Staff ViewISSN: 1573-8205Source: Springer Online Journal Archives 1860-2000Topics: Energy, Environment Protection, Nuclear Power EngineeringPhysicsType of Medium: Electronic ResourceURL: -
4Articles: DFG German National LicensesMatishov, G. G. ; Druzhkov, N. V. ; Namyatov, A. A. ; Marasaeva, E. F. ; Larionov, V. V. ; Moiseev, D. V. ; Bronnikov, I. V. ; Ishkulova, T. G.
Springer
Published 2000Staff ViewISSN: 1608-3105Source: Springer Online Journal Archives 1860-2000Topics: BiologyType of Medium: Electronic ResourceURL: -
5Articles: DFG German National LicensesStaff View
ISSN: 1573-8353Keywords: 1-alkyl-3-(quinolyl)quinolinium halides ; 2,3-biquinolyl ; 1,4-dihydro-2,3-biquinolyls ; 1,2-dihydro-2,3-biquinolyls ; sodium borohydride ; nucleophilic addition ; regioselectivitySource: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract Reduction of 1-alkyl-3-(2-quinolyl)quinolinium halides with sodium borohydride leads to 1′-alkyl-1′,2′-dihydro-2,3′-biquinolyls which, except for the ethoxycarbonyl derivative, undergo rearrangement to 1′-alkyl-1′,4′-dihydro-2,3′-biquinolyls. The last can be synthesized by the alkylation of the corresponding 1′,4′-dihydro-2,3′-biquinolyls under conditions of interphase catalysis and in the system KOH-DMSO.Type of Medium: Electronic ResourceURL: -
6Articles: DFG German National LicensesStaff View
ISSN: 1573-8353Source: Springer Online Journal Archives 1860-2000Topics: Chemistry and PharmacologyNotes: Abstract Nucleophilic addition of organometallic lithium and magnesium compounds to 1-alkyl-3-(2-quinolyl)quinolinium cations produces a mixture of the corresponding 1′-alkyl-2′-R-1′,2′-dihydro-2,3′-biquinolyls and 1′-alkyl-4′-R-1′,4′-dihydro-2,3′-biquinolyls. The portion of the latter decreases with increasing “hardness” of the organometallic compound.Type of Medium: Electronic ResourceURL: