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Publications in Math-Net.Ru |
Citations |
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2018 |
| 1. |
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   |
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2017 |
| 2. |
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 |
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2016 |
| 3. |
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 |
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2015 |
| 4. |
A. A. Grachev, M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Facile reaction of bis(tri-<i>n</i>-butyltin) oxide with silica gel”, Mendeleev Commun., 25:1 (2015), 51–53 |
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2013 |
| 5. |
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 |
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2012 |
| 6. |
I. M. Kumanyaev, M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “Pyridinium <i>o</i>-iodoxybenzoate as a Safe form of a Famous Oxidant”, Mendeleev Commun., 22:3 (2012), 129–131 |
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2010 |
| 7. |
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 |
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2008 |
| 8. |
M. A. Lapitskaya, L. L. Vasiljeva, K. K. Pivnitsky, “<i>o</i>-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 |
| 9. |
M. A. Lapitskaya, G. V. Zatonsky, K. K. Pivnitsky, “Enantiomeric NMR analysis of chiral epoxides as addition compounds with <i>d</i>-ephedrine”, Mendeleev Commun., 15:5 (2005), 175–178 |
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2004 |
| 10. |
M. A. Lapitskaya, L. L. Vasiljeva, P. M. Demin, K. K. Pivnitsky, “Total synthesis of trioxilins 11,12-<i>threo</i>-(8,11,12)-A<sub>3</sub> through type B<sub>3</sub> trioxilins”, Mendeleev Commun., 14:6 (2004), 291–293 |
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| 11. |
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 |
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2000 |
| 12. |
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 |
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1999 |
| 13. |
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 |
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