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  1. 2017

  2. Structure and photoluminescence of Zn(II) and Сd(II) complexes with chiral bis-pyridine containing fragments of natural (–)-α-pinene

    Kokina, T. E., Glinskaya, L. A., Vasiliev, E. S., Rakhmanova, M. I., Makarova, S. V., Piryazev, D. A., Korol’kov, I. V., Tkachev, A. V. & Larionov, S. V., 1 Sept 2017, In: Journal of Structural Chemistry. 58, 5, p. 994-1003 10 p.

    Research output: Contribution to journal › Article › peer-review

  3. Ln(III) complexes (Ln = Eu, Gd, Tb, Dy) with a chiral ligand containing 1,10-phenanthroline and (-)-menthol fragments: Synthesis, structure, magnetic properties and photoluminescence

    Larionov, S. V., Bryleva, Y. A., Glinskaya, L. A., Plyusnin, V. F., Kupryakov, A. S., Agafontsev, A. M., Tkachev, A. V., Bogomyakov, A. S., Piryazev, D. A. & Korolkov, I. V., 29 Aug 2017, In: Dalton Transactions. 46, 34, p. 11440-11450 11 p.

    Research output: Contribution to journal › Article › peer-review

  4. Complexes PdCl2 with optically active hybrid ligands built of α-pinene and β-alanine molecules

    Kokina, T. E., Glinskaya, L. A., Marenin, K. S., Korol’kov, I. V., Naumov, D. Y., Tkachev, A. V. & Larionov, S. V., 1 Apr 2017, In: Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya. 43, 4, p. 213-222 10 p.

    Research output: Contribution to journal › Article › peer-review

  5. Syntheses of chiral nopinane-annelated pyridines of C2 and D2-symmetry: X-ray structures of the fused derivatives of 4,5-diazafluorene, 4,5-diaza-9H-fluoren-9-one, and 9,9’-bi-4,5-diazafluorenylidene

    Vasilyev, E. S., Bagryanskaya, I. Y. & Tkachev, A. V., 1 Mar 2017, In: Mendeleev Communications. 27, 2, p. 128-130 3 p.

    Research output: Contribution to journal › Article › peer-review

  6. Stereoselectivity of formation of monoterpene – Amino acids hybrid molecules in the reaction of monoterpene nitroso chlorides with α-amino acid derivatives

    Marenin, K. S., Gatilov, Y. V., Agafontsev, A. M. & Tkachev, A. V., 1 Jan 2017, In: Steroids. 117, p. 112-119 8 p.

    Research output: Contribution to journal › Article › peer-review

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