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Публикации в базе данных Math-Net.Ru |
Цитирования |
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2020 |
| 1. |
M. V. Zlokazov, K. K. Pivnitsky, “Lamellar conglomerates”, Mendeleev Commun., 30:1 (2020), 1–6   |
10
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2019 |
| 2. |
N. S. Vostrikov, L. V. Spirikhin, A. N. Lobov, A. M. Gimazetdinov, Z. R. Zileeva, Yu. V. Vakhitova, Z. R. Macaev, K. K. Pivnitsky, M. S. Miftakhov, “Simple antitumor model compounds for cross-conjugated cyclopentenone prostaglandins”, Mendeleev Commun., 29:4 (2019), 372–374 |
11
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| 3. |
V. P. Kislyi, Ya. V. Zubavichus, K. K. Babievsky, V. N. Khrustalev, K. K. Pivnitsky, “Racemic estrone methyl ether is the lamellar conglomerate”, Mendeleev Commun., 29:3 (2019), 256–259 |
2
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| 4. |
V. A. Vil', E. S. Gorlov, O. V. Bityukov, I. B. Krylov, G. I. Nikishin, K. K. Pivnitsky, A. O. Terent'ev, “Oxidative C–O coupling as a new idea in the 'click-like chemistry': malonyl peroxides for the conjugation of two molecules”, Mendeleev Commun., 29:2 (2019), 132–134 |
2
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2018 |
| 5. |
M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Dimethylmalonoyl peroxide – the neglected lowest homologue: simple synthesis and high reactivity”, Mendeleev Commun., 28:5 (2018), 505–507 |
2
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2017 |
| 6. |
M. A. Lapitskaya, V. A. Vil', L. L. Vasiljeva, E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Spontaneous reaction of malonyl peroxides with methanol”, Mendeleev Commun., 27:3 (2017), 243–245 |
3
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| 7. |
N. S. Vostrikov, I. F. Lobko, L. V. Spirikhin, Yu. V. Vakhitova, K. K. Pivnitsky, M. S. Miftakhov, “Side-modified 15-deoxy-Δ<sup>12,14</sup>-prostaglandin D<sub>2</sub>, precursor of corresponding PGJ<sub>2</sub>. Synthesis from cloprostenol and anticancer activity”, Mendeleev Commun., 27:2 (2017), 125–127 |
9
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2016 |
| 8. |
M. A. Lapitskaya, V. A. Vil', E. D. Daeva, A. O. Terent'ev, K. K. Pivnitsky, “Alcoholysis of malonyl peroxides to give peracids”, Mendeleev Commun., 26:1 (2016), 14–15 |
7
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2015 |
| 9. |
A. A. Grachev, M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Facile reaction of bis(tri-n-butyltin) oxide with silica gel”, Mendeleev Commun., 25:1 (2015), 51–53 |
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2014 |
| 10. |
A. O. Terent'ev, V. A. Vil', O. M. Mulina, K. K. Pivnitsky, G. I. Nikishin, “A convenient synthesis of cyclopropane malonyl peroxide”, Mendeleev Commun., 24:6 (2014), 345 |
16
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| 11. |
Z. R. Valiullina, L. S. Khasanova, N. K. Selezneva, F. A. Gimalova, K. K. Pivnitsky, M. S. Miftakhov, “Unexpected fragmentation of 16β-acetoxy-22-oxocholestanes on the action of methylenetriphenylphosphorane”, Mendeleev Commun., 24:5 (2014), 272–273 |
1
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2013 |
| 12. |
M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Potassium fluoride on calcium fluoride – a practical reagent for removal of organotin residues from reaction mixtures”, Mendeleev Commun., 23:5 (2013), 257–259 |
7
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2012 |
| 13. |
I. M. Kumanyaev, M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Pyridinium o-iodoxybenzoate as a Safe form of a Famous Oxidant”, Mendeleev Commun., 22:3 (2012), 129–131 |
9
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2010 |
| 14. |
M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Practical synthesis of 16,22-diketocholesterol acetate, a precursor of anticancer saponin OSW-1, from diosgenin”, Mendeleev Commun., 20:6 (2010), 318–320 |
2
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2008 |
| 15. |
M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “o-Iodoxybenzoic acid in dimethylformamide as a convenient reagent for the oxidation of alcohols to aldehydes and ketones”, Mendeleev Commun., 18:6 (2008), 309–311 |
16
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2005 |
| 16. |
M. A. Lapitskaya, G. V. Zatonsky, K. K. Pivnitsky, “Enantiomeric NMR analysis of chiral epoxides as addition compounds with d-ephedrine”, Mendeleev Commun., 15:5 (2005), 175–178 |
2
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2004 |
| 17. |
M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Total synthesis of trioxilins 11,12-threo-(8,11,12)-A<sub>3</sub> through type B<sub>3</sub> trioxilins”, Mendeleev Commun., 14:6 (2004), 291–293 |
3
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| 18. |
M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Enantiodivergent total synthesis of trioxilins B<sub>3</sub> using Sharpless asymmetric olefin dihydroxylation”, Mendeleev Commun., 14:6 (2004), 287–290 |
4
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2000 |
| 19. |
M. A. Lapitskaya, L. L. Vasiljeva, G. V. Zatonsky, K. K. Pivnitsky, “Synthesis of series 2 trioxilins from trioxilin B<sub>3</sub> by selective hydrogenation”, Mendeleev Commun., 10:4 (2000), 130–131 |
3
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1999 |
| 20. |
M. A. Lapitskaya, G. V. Zatonsky, K. K. Pivnitsky, “Enantiomeric NMR analysis of organic acids with the Corey chiral controller”, Mendeleev Commun., 9:4 (1999), 149–151 |
4
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1997 |
| 21. |
P. M. Demin, D. M. Kochev, H. Perrier, C. R. Pace-Asciak, K. K. Pivnitsky, “Synthesis of a photoaffinic hepoxilin analog”, Mendeleev Commun., 7:3 (1997), 90–91 |
4
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1996 |
| 22. |
L. L. Vasiljeva, K. K. Pivnitsky, “Synthesis of trioxilins B<sub>3</sub> from hepoxilins B<sub>3</sub>”, Mendeleev Commun., 6:6 (1996), 251–252 |
7
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| 23. |
P. M. Demin, T. A. Manukina, C. R. Pace-Asciak, K. K. Pivnitsky, “Total synthesis of 20-hydroxy-hepoxilins, new metabolites of the hepoxilin family”, Mendeleev Commun., 6:4 (1996), 130–132 |
8
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1960 |
| 24. |
И. К. Коробицына, К. К. Пивницкий, “Новый метод синтеза 2,2,6,6-тетраалкилтетрагидропирандионов-3,5”, Докл. АН СССР, 132:1 (1960), 127–129 |
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