1 Wiley
NMR and DFT investigations of the substituent and solvent effect on amino - imino tautomerism in acridin-9-amines substituted at the exocyclic nitrogen atom
Youssif Ebead, Agnieszka Wro'blewska, Karol Krzymiski, Janusz Rak, Jerzy Baejowski
Journal of Physical Organic Chemistry Volume 18 Issue 8, Pages 870 - 879
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http://dx.doi.org/10.1002/poc.956Synthesis and properties of oligodeoxyribonucleotides containing 2’-O-(2,3-dihydroxypropyl)- and 2’-O-(2-oxoethyl)arabinouridine residues
T. S. Zatsepin
Russian Chemical Bulletin Volume 54, Number 1 / Январь 2005 г.238-246
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http://dx.doi.org/10.1007/s11172-005-0243-29-Isothiocyanatoacridines: Convenient synthons for new functionalized 9-acridinyl derivatives
Kristian,P.
Molecules Volume 1, Number 10 / Февраль 1997 г. 181-189
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http://dx.doi.org/10.1007/s007830050036864. Acridine syntheses and reactions. Part VI. A new dehalogenation of 9-chloroacridine and its derivatives. Further acridine ionisation constants and ultraviolet spectra
Albert,A.
J.Chem.Society (Resumed) 4653 - 4657
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http://dx.doi.org/10.1039/JR9650004653