A. V. Gulevich

发表

Synthetic Application of Isocyanoacetic Acid Derivatives

V. Nenajdenko, R. Orru, A. V. Gulevich, 2012 .

Chiral Isocyanoazides: Efficient Bifunctional Reagents for Bioconjugation

V. Nenajdenko, E. Balenkova, A. V. Gulevich, 2010 .

Versatile reactivity of rhodium-iminocarbenes derived from N-sulfonyl triazoles.

V. Gevorgyan, A. V. Gulevich, 2013, Angewandte Chemie.

Novel Reagents for Multi-Component Reactions

I. V. Plekhanova, A. V. Popov, V. A. Glushkov, 2011 .

Synthesis of Multisubstituted Arenes via PyrDipSi-Directed Unsymmetrical Iterative C–H Functionalizations

Ferdinand S. Melkonyan, V. Gevorgyan, D. Sarkar, 2015 .

The Ugi reaction with 2-substituted cyclic imines. Synthesis of substituted proline and homoproline derivatives

V. Nenajdenko, E. Balenkova, A. V. Gulevich, 2006 .

One-step synthesis of N-acetylcysteine and glutathione derivatives using the Ugi reaction

V. Nenajdenko, A. V. Gulevich, Alexander G Zhdanko, 2009 .

Double-fold C-H oxygenation of arenes using PyrDipSi: a general and efficient traceless/modifiable silicon-tethered directing group.

Ferdinand S. Melkonyan, V. Gevorgyan, D. Sarkar, 2012, Journal of the American Chemical Society.

The Passerini Reaction with CF3‐Carbonyl Compounds – Multicomponent Approach to Trifluoromethyl Depsipeptides

V. Nenajdenko, A. V. Gulevich, Inga V. Shpilevaya, 2009 .

Multicomponent synthesis of artificial nucleases and their RNase and DNase activity

O. Morozova, V. Silnikov, V. Nenajdenko, 2011, Beilstein journal of organic chemistry.

Rhodium-catalyzed NH insertion of pyridyl carbenes derived from pyridotriazoles: a general and efficient approach to 2-picolylamines and imidazo[1,5-a]pyridines.

V. Gevorgyan, Yi Shi, A. V. Gulevich, 2014, Angewandte Chemie.

Isocyanoacetate derivatives: synthesis, reactivity, and application.

V. Nenajdenko, R. Orru, A. V. Gulevich, 2010, Chemical reviews.

Transition metal-mediated synthesis of monocyclic aromatic heterocycles.

A. S. Dudnik, V. Gevorgyan, A. V. Gulevich, 2013, Chemical reviews.

The Ugi reaction with CF3-carbonyl compounds: effective synthesis of α-trifluoromethyl amino acid derivatives

G. Röschenthaler, V. Nenajdenko, E. Balenkova, 2008 .

The first example of a diastereoselective thio-Ugi reaction: a new synthetic approach to chiral imidazole derivatives.

V. Nenajdenko, E. Balenkova, A. V. Gulevich, 2007, The Journal of organic chemistry.

Conversion of 1-alkenes into 1,4-diols through an auxiliary-mediated formal homoallylic C–H oxidation

Chunhui Huang, Ferdinand S. Melkonyan, V. Gevorgyan, 2014, Nature chemistry.

General and practical carboxyl-group-directed remote C-H oxygenation reactions of arenes.

V. Gevorgyan, Yang Wang, A. V. Gulevich, 2013, Chemistry.

Twofold unsymmetrical C-H functionalization of PyrDipSi-substituted arenes: a general method for the synthesis of substituted meta-halophenols.

Ferdinand S. Melkonyan, V. Gevorgyan, D. Sarkar, 2013, Angewandte Chemie.

A new reactivity mode for the diazo group: diastereoselective 1,3-aminoalkylation reaction of β-amino-α-diazoesters to give triazolines.

D. Wink, V. Gevorgyan, A. Kuznetsov, 2014, Angewandte Chemie.

Pyridine group assisted addition of diazo-compounds to imines in the 3-CC reaction of 2-aminopyridines, aldehydes, and diazo-compounds.

D. Wink, V. Gevorgyan, A. V. Gulevich, 2013, Organic letters.

Efficient Multicomponent Synthesis of α-Trifluoromethyl Proline, Homoproline, and Azepan Carboxylic Acid Dipeptides

G. Röschenthaler, V. Nenajdenko, E. Balenkova, 2009 .

R-α-Phenylglycinol and R-α-phenylglycinamide as novel chiral templates in diastereoselective Ugi reaction

V. Nenajdenko, K. Chernichenko, E. Balenkova, 2011 .

Cu-catalyzed transannulation reaction of pyridotriazoles with terminal alkynes under aerobic conditions: efficient synthesis of indolizines

V. Gevorgyan, A. V. Gulevich, V. Helan, 2015, Chemical science.

Design of Multi-Component Reactions

A. S. Medvedeva, Alexey P. Ilyin, V. A. Glushkov, 2011 .

Conversion of 1‐Alkenes into 1,4‐Diols Through an Auxiliary‐Mediated Formal Homoallylic C—H Oxidation.

Chunhui Huang, Ferdinand S. Melkonyan, V. Gevorgyan, 2014 .