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Synthetic Model of the Phosphate Binding Protein:  Solid-State Structure and Solution-Phase Anion Binding Properties of a Large Oligopyrrolic Macrocycle
Synthetic Model of the Phosphate Binding Protein:  Solid-State Structure and Solution-Phase Anion Binding Properties of a Large Oligopyrrolic Macrocycle
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Synthetic Model of the Phosphate Binding Protein:  Solid-State Structure and Solution-Phase Anion Binding Properties of a Large Oligopyrrolic Macrocycle

Katayev, Evgeny A ; Sessler, Jonathan L ; Khrustalev, Victor N ; Ustynyuk, Yuri A

Journal of organic chemistry, 2007-09, Vol.72 (19), p.7244-7252 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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2
Highly Stereoselective and Scalable Synthesis of trans-Fused Octahydrocyclohepta[b]pyrrol-4(1H)‑ones via the Aza-Cope–Mannich Rearrangement in Racemic and Enantiopure Forms
Highly Stereoselective and Scalable Synthesis of trans-Fused Octahydrocyclohepta[b]pyrrol-4(1H)‑ones via the Aza-Cope–Mannich Rearrangement in Racemic and Enantiopure Forms
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Highly Stereoselective and Scalable Synthesis of trans-Fused Octahydrocyclohepta[b]pyrrol-4(1H)‑ones via the Aza-Cope–Mannich Rearrangement in Racemic and Enantiopure Forms

Belov, Dmitry S ; Lukyanenko, Evgeny R ; Kurkin, Alexander V ; Yurovskaya, Marina A

Journal of organic chemistry, 2012-11, Vol.77 (22), p.10125-10134 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
Preparation and X-ray Structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic Acid and 3-[Hydroxy(tosyloxy)iodo]benzoic Acid:  New Recyclable Hypervalent Iodine Reagents
Preparation and X-ray Structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic Acid and 3-[Hydroxy(tosyloxy)iodo]benzoic Acid:  New Recyclable Hypervalent Iodine Reagents
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Preparation and X-ray Structures of 3-[Bis(trifluoroacetoxy)iodo]benzoic Acid and 3-[Hydroxy(tosyloxy)iodo]benzoic Acid:  New Recyclable Hypervalent Iodine Reagents

Yusubov, Mekhman S ; Funk, Tatyana V ; Chi, Ki-Whan ; Cha, Eun-Hye ; Kim, Ghyung Hwa ; Kirschning, Andreas ; Zhdankin, Viktor V

Journal of organic chemistry, 2008-01, Vol.73 (1), p.295-297 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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4
The First Example of a Diastereoselective Thio-Ugi Reaction:  A New Synthetic Approach to Chiral Imidazole Derivatives
The First Example of a Diastereoselective Thio-Ugi Reaction:  A New Synthetic Approach to Chiral Imidazole Derivatives
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The First Example of a Diastereoselective Thio-Ugi Reaction:  A New Synthetic Approach to Chiral Imidazole Derivatives

Gulevich, Anton V ; Balenkova, Elizabeth S ; Nenajdenko, Valentine G

Journal of organic chemistry, 2007-10, Vol.72 (21), p.7878-7885 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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5
Dissecting Alkynes: Full Cleavage of Polarized CC Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
Dissecting Alkynes: Full Cleavage of Polarized CC Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade
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Dissecting Alkynes: Full Cleavage of Polarized CC Moiety via Sequential Bis-Michael Addition/Retro-Mannich Cascade

Roy, Saumya ; Davydova, Maria P ; Pal, Runa ; Gilmore, Kerry ; Tolstikov, Genrikh A ; Vasilevsky, Sergei F ; Alabugin, Igor V

Journal of organic chemistry, 2011-09, Vol.76 (18), p.7482-7490 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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6
A General and Convenient Preparation of [Bis(trifluoroacetoxy)iodo]perfluoroalkanes and [Bis(trifluoroacetoxy)iodo]arenes by Oxidation of Organic Iodides Using Oxone and Trifluoroacetic Acid
A General and Convenient Preparation of [Bis(trifluoroacetoxy)iodo]perfluoroalkanes and [Bis(trifluoroacetoxy)iodo]arenes by Oxidation of Organic Iodides Using Oxone and Trifluoroacetic Acid
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A General and Convenient Preparation of [Bis(trifluoroacetoxy)iodo]perfluoroalkanes and [Bis(trifluoroacetoxy)iodo]arenes by Oxidation of Organic Iodides Using Oxone and Trifluoroacetic Acid

Zagulyaeva, Aleksandra A ; Yusubov, Mekhman S ; Zhdankin, Viktor V

Journal of organic chemistry, 2010-03, Vol.75 (6), p.2119-2122 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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7
Enantioselective Intramolecular Hydroamination Catalyzed by Lanthanide Ate Complexes Coordinated by N-Substituted (R)-1,1‘-Binaphthyl-2,2‘-diamido Ligands
Enantioselective Intramolecular Hydroamination Catalyzed by Lanthanide Ate Complexes Coordinated by N-Substituted (R)-1,1‘-Binaphthyl-2,2‘-diamido Ligands
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Enantioselective Intramolecular Hydroamination Catalyzed by Lanthanide Ate Complexes Coordinated by N-Substituted (R)-1,1‘-Binaphthyl-2,2‘-diamido Ligands

Riegert, David ; Collin, Jacqueline ; Meddour, Abdelkrim ; Schulz, Emmanuelle ; Trifonov, Alexander

Journal of organic chemistry, 2006-03, Vol.71 (6), p.2514-2517 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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8
Porphyrins in 1,3-Dipolar Cycloaddition Reactions. Synthesis of New Porphyrin−Chlorin and Porphyrin−Tetraazachlorin Dyads
Porphyrins in 1,3-Dipolar Cycloaddition Reactions. Synthesis of New Porphyrin−Chlorin and Porphyrin−Tetraazachlorin Dyads
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Porphyrins in 1,3-Dipolar Cycloaddition Reactions. Synthesis of New Porphyrin−Chlorin and Porphyrin−Tetraazachlorin Dyads

Silva, Ana M. G ; Lacerda, Paula S. S ; Tomé, Augusto C ; Neves, Maria G. P. M. S ; Silva, Artur M. S ; Cavaleiro, José A. S ; Makarova, Elena A ; Lukyanets, Evgeny A

Journal of organic chemistry, 2006-10, Vol.71 (22), p.8352-8356 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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9
New Four-Component Ugi-Type Reaction. Synthesis of Heterocyclic Structures Containing a Pyrrolo[1,2-a][1,4]diazepine Fragment
New Four-Component Ugi-Type Reaction. Synthesis of Heterocyclic Structures Containing a Pyrrolo[1,2-a][1,4]diazepine Fragment
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New Four-Component Ugi-Type Reaction. Synthesis of Heterocyclic Structures Containing a Pyrrolo[1,2-a][1,4]diazepine Fragment

Ilyn, Alexey P ; Trifilenkov, Andrey S ; Kuzovkova, Julia A ; Kutepov, Sergey A ; Nikitin, Alexandre V ; Ivachtchenko, Alexandre V

Journal of organic chemistry, 2005-02, Vol.70 (4), p.1478-1481 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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10
Bisaziridine Tetracarboxylates as Building Blocks in the Stereoselective Synthesis of C60-Fullerene Diads and Dumbbell-like Bis-C60-fullerene Triads
Bisaziridine Tetracarboxylates as Building Blocks in the Stereoselective Synthesis of C60-Fullerene Diads and Dumbbell-like Bis-C60-fullerene Triads
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Bisaziridine Tetracarboxylates as Building Blocks in the Stereoselective Synthesis of C60-Fullerene Diads and Dumbbell-like Bis-C60-fullerene Triads

Konev, Alexander S ; Khlebnikov, Alexander F ; Frauendorf, Holm

Journal of organic chemistry, 2011-08, Vol.76 (15), p.6218-6229 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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