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Publications in Math-Net.Ru |
Citations |
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2015 |
1. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Efficient synthesis of tertiary acyclic amides by the Chapman rearrangement of aryl benzimidates in ionic liquids”, Mendeleev Commun., 25:2 (2015), 126–128 |
6
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2. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Nucleophilic aromatic <i>cine</i>-substitution of hydrogen: the ionic liquid-promoted von Richter reaction”, Mendeleev Commun., 25:1 (2015), 41–43 |
9
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2012 |
3. |
N. I. Simirskaya, N. V. Ignat'ev, M. Schulte, S. G. Zlotin, “Mannich Synthesis of Acetylenic Amino Alcohols in Aqueous Ionic Liquids”, Mendeleev Commun., 22:6 (2012), 317–319 |
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4. |
M. A. Epishina, A. S. Kulikov, M. I. Struchkova, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Ionic Liquids-assisted Synthesis of 3,4-Dihydroisoquinolines by the Bishler–Napieralski Reaction”, Mendeleev Commun., 22:5 (2012), 267–269 |
5
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5. |
A. B. Sheremetev, N. S. Aleksandrova, N. V. Ignat'ev, M. Schulte, “Straightforward one-pot synthesis of benzofuroxans from o-halonitrobenzenes in ionic liquids”, Mendeleev Commun., 22:2 (2012), 95–97 |
18
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2011 |
6. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Ionic liquid-assisted synthesis of 5-monoand 1,5-disubstituted tetrazoles”, Mendeleev Commun., 21:6 (2011), 334–336 |
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7. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “Synthesis of 5-alkyl-2-amino-1,3,4-thiadiazoles and α,ω-bis(2-amino-1,3,4-thiadiazol-5-yl)alkanes in ionic liquids”, Mendeleev Commun., 21:6 (2011), 331–333 |
21
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8. |
N. I. Simirskaya, N. V. Ignat'ev, M. Schulte, S. G. Zlotin, “Unprecedented acceleration of the domino reaction between methyl 4-hydroxyalk-3-ynoates and amines in ionic liquids”, Mendeleev Commun., 21:2 (2011), 94–96 |
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2010 |
9. |
M. A. Epishina, A. S. Kulikov, N. V. Ignat'ev, M. Schulte, N. N. Makhova, “The first example of the Schmidt reaction in ionic liquids”, Mendeleev Commun., 20:6 (2010), 335–336 |
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