Transition metal-mediated synthesis of monocyclic aromatic heterocycles AV Gulevich, AS Dudnik, N Chernyak, V Gevorgyan Chemical reviews 113 (5), 3084-3213, 2013 | 736 | 2013 |
Isocyanoacetate derivatives: synthesis, reactivity, and application AV Gulevich, AG Zhdanko, RVA Orru, VG Nenajdenko Chemical reviews 110 (9), 5235-5331, 2010 | 456 | 2010 |
Versatile Reactivity of Rhodium–Iminocarbenes Derived from N‐Sulfonyl Triazoles AV Gulevich, V Gevorgyan Angewandte Chemie International Edition 52 (5), 1371-1373, 2013 | 258 | 2013 |
Double-fold C–H oxygenation of arenes using PyrDipSi: a general and efficient traceless/modifiable silicon-tethered directing group AV Gulevich, FS Melkonyan, D Sarkar, V Gevorgyan Journal of the American Chemical Society 134 (12), 5528-5531, 2012 | 119 | 2012 |
Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: efficient synthesis of indolizines V Helan, AV Gulevich, V Gevorgyan Chemical Science 6 (3), 1928-1931, 2015 | 107 | 2015 |
Conversion of 1-alkenes into 1, 4-diols through an auxiliary-mediated formal homoallylic C–H oxidation N Ghavtadze, FS Melkonyan, AV Gulevich, C Huang, V Gevorgyan Nature chemistry 6 (2), 122-125, 2014 | 83 | 2014 |
General and Practical Carboxyl‐Group‐Directed Remote C H Oxygenation Reactions of Arenes Y Wang, AV Gulevich, V Gevorgyan Chemistry–A European Journal 19 (47), 15836-15840, 2013 | 82 | 2013 |
Rhodium‐Catalyzed NH Insertion of Pyridyl Carbenes Derived from Pyridotriazoles: A General and Efficient Approach to 2‐Picolylamines and Imidazo [1, 5‐a] pyridines Y Shi, AV Gulevich, V Gevorgyan Angewandte Chemie International Edition 53 (51), 14191-14195, 2014 | 76 | 2014 |
Twofold Unsymmetrical CH Functionalization of PyrDipSi‐Substituted Arenes: A General Method for the Synthesis of Substituted meta‐Halophenols D Sarkar, FS Melkonyan, AV Gulevich, V Gevorgyan Angewandte Chemie 125 (41), 11000-11004, 2013 | 73 | 2013 |
The Ugi reaction with 2-substituted cyclic imines. Synthesis of substituted proline and homoproline derivatives VG Nenajdenko, AV Gulevich, ES Balenkova Tetrahedron 62 (25), 5922-5930, 2006 | 73 | 2006 |
The first example of a diastereoselective thio-Ugi reaction: A new synthetic approach to chiral imidazole derivatives AV Gulevich, ES Balenkova, VG Nenajdenko The Journal of organic chemistry 72 (21), 7878-7885, 2007 | 67 | 2007 |
The Ugi reaction with CF3-carbonyl compounds: effective synthesis of α-trifluoromethyl amino acid derivatives AV Gulevich, NE Shevchenko, ES Balenkova, GV Roeschenthaler, ... Tetrahedron 64 (51), 11706-11712, 2008 | 62 | 2008 |
Synthesis of multisubstituted arenes via pyrdipsi-directed unsymmetrical iterative c–h functionalizations D Sarkar, AV Gulevich, FS Melkonyan, V Gevorgyan ACS Catalysis 5 (11), 6792-6801, 2015 | 50 | 2015 |
Chiral isocyanoazides: Efficient bifunctional reagents for bioconjugation VG Nenajdenko, AV Gulevich, NV Sokolova, AV Mironov, ES Balenkova European Journal of Organic Chemistry 2010 (8), 1445-1449, 2010 | 49 | 2010 |
One-step synthesis of N-acetylcysteine and glutathione derivatives using the Ugi reaction AG Zhdanko, AV Gulevich, VG Nenajdenko Tetrahedron 65 (24), 4692-4702, 2009 | 47 | 2009 |
Rhodiumiminocarbene aus N‐Sulfonyltriazolen: vielseitig abstimmbare Reaktivität AV Gulevich, V Gevorgyan Angewandte Chemie 125 (5), 1411-1413, 2013 | 44 | 2013 |
Efficient multicomponent synthesis of α-trifluoromethyl proline, homoproline, and azepan carboxylic acid dipeptides AV Gulevich, NE Shevchenko, ES Balenkova, GV Roeschenthaler, ... Synlett 2009 (03), 403-406, 2009 | 39 | 2009 |
Pyridine group assisted addition of diazo-compounds to imines in the 3-CC Reaction of 2-aminopyridines, aldehydes, and diazo-compounds AV Gulevich, V Helan, DJ Wink, V Gevorgyan Organic letters 15 (4), 956-959, 2013 | 29 | 2013 |
The Passerini Reaction with CF3‐Carbonyl Compounds – Multicomponent Approach to Trifluoromethyl Depsipeptides AV Gulevich, IV Shpilevaya, VG Nenajdenko European Journal of Organic Chemistry 2009 (22), 3801-3808, 2009 | 25 | 2009 |
A New Reactivity Mode for the Diazo Group: Diastereoselective 1, 3‐Aminoalkylation Reaction of β‐Amino‐α‐Diazoesters To Give Triazolines A Kuznetsov, AV Gulevich, DJ Wink, V Gevorgyan Angewandte Chemie International Edition 53 (34), 9021-9025, 2014 | 24 | 2014 |