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Refinado por: Nome da Publicação: The Journal Of Organic Chemistry remover idioma: Russo remover Japonês remover
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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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12
First Synthesis of Pentasaccharide Glycoform I of the Outer Core Region of the Pseudomonas aeruginosa Lipopolysaccharide
First Synthesis of Pentasaccharide Glycoform I of the Outer Core Region of the Pseudomonas aeruginosa Lipopolysaccharide
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First Synthesis of Pentasaccharide Glycoform I of the Outer Core Region of the Pseudomonas aeruginosa Lipopolysaccharide

Komarova, Bozhena S ; Tsvetkov, Yury E ; Pier, Gerald B ; Nifantiev, Nikolay E

Journal of organic chemistry, 2008-11, Vol.73 (21), p.8411-8421 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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13
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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14
The 2-Oxocyclobutanecarboxylic Acid Keto−Enol System in Aqueous Solution:  A Remarkable Acid-Strengthening Effect of the Cyclobutane Ring
The 2-Oxocyclobutanecarboxylic Acid Keto−Enol System in Aqueous Solution:  A Remarkable Acid-Strengthening Effect of the Cyclobutane Ring
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The 2-Oxocyclobutanecarboxylic Acid Keto−Enol System in Aqueous Solution:  A Remarkable Acid-Strengthening Effect of the Cyclobutane Ring

Chang, J. A ; Chiang, Y ; Keeffe, J. R ; Kresge, A. J ; Nikolaev, V. A ; Popik, V. V

Journal of organic chemistry, 2006-06, Vol.71 (12), p.4460-4467 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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15
New .pi.-Donor Precursor Molecule for the Preparation of Organic Metals, 4,5;4',5'-Bis(1,4-dioxanediyl-2,3-dithio)tetrathiafulvalene: Synthesis and Properties
New .pi.-Donor Precursor Molecule for the Preparation of Organic Metals, 4,5;4',5'-Bis(1,4-dioxanediyl-2,3-dithio)tetrathiafulvalene: Synthesis and Properties
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New .pi.-Donor Precursor Molecule for the Preparation of Organic Metals, 4,5;4',5'-Bis(1,4-dioxanediyl-2,3-dithio)tetrathiafulvalene: Synthesis and Properties

Kotov, Alexander I ; Faulmann, Christophe ; Cassoux, Patrick ; Yagubskii, Eduard B

Journal of organic chemistry, 1994-05, Vol.59 (9), p.2626-2629 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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