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1
1-(2,3,4-trimethoxyphenyl)-3-(3-(2-chloroquinolinyl))-2-propen-1-one, a chalcone derivative with analgesic, anti-inflammatory and immunomodulatory properties
1-(2,3,4-trimethoxyphenyl)-3-(3-(2-chloroquinolinyl))-2-propen-1-one, a chalcone derivative with analgesic, anti-inflammatory and immunomodulatory properties
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1-(2,3,4-trimethoxyphenyl)-3-(3-(2-chloroquinolinyl))-2-propen-1-one, a chalcone derivative with analgesic, anti-inflammatory and immunomodulatory properties

De León, E J ; Alcaraz, M J ; Dominguez, J N ; Charris, J ; Terencio, M C

Inflammation research, 2003-06, Vol.52 (6), p.246-257 [Periódico revisado por pares]

Switzerland: Springer Nature B.V

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2
1,1-Dioxonaphtho[1,2-b]thiophene-2-methyloxycarbonyl (α-Nsmoc) and 3,3-Dioxonaphtho[2,1-b]thiophene-2-methyloxycarbonyl (β-Nsmoc) Amino-Protecting Groups
1,1-Dioxonaphtho[1,2-b]thiophene-2-methyloxycarbonyl (α-Nsmoc) and 3,3-Dioxonaphtho[2,1-b]thiophene-2-methyloxycarbonyl (β-Nsmoc) Amino-Protecting Groups
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1,1-Dioxonaphtho[1,2-b]thiophene-2-methyloxycarbonyl (α-Nsmoc) and 3,3-Dioxonaphtho[2,1-b]thiophene-2-methyloxycarbonyl (β-Nsmoc) Amino-Protecting Groups

Carpino, Louis A ; Abdel-Maksoud, Adel Ali ; Ionescu, Dumitru ; Mansour, E. M. E ; Zewail, Mohamed A

Journal of organic chemistry, 2007-03, Vol.72 (5), p.1729-1736 [Periódico revisado por pares]

Washington, DC: American Chemical Society

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3
1,1-Diphenyl-2-picrylhydrazyl radical-scavenging active compounds from greater cardamom (Amomum subulatum Roxb.)
1,1-Diphenyl-2-picrylhydrazyl radical-scavenging active compounds from greater cardamom (Amomum subulatum Roxb.)
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1,1-Diphenyl-2-picrylhydrazyl radical-scavenging active compounds from greater cardamom (Amomum subulatum Roxb.)

Kikuzaki, H. (Osaka City Univ. (Japan)) ; Kawai, Y ; Nakatani, N

Journal of Nutritional Science and Vitaminology, 2001, Vol.47(2), pp.167-171 [Periódico revisado por pares]

Tokyo: Center for Academic Publications Japan

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4
1,1'-Linked Cyclopropane Derivatives: The Helical Conformation of Quinquecyclopropanol
1,1'-Linked Cyclopropane Derivatives: The Helical Conformation of Quinquecyclopropanol
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1,1'-Linked Cyclopropane Derivatives: The Helical Conformation of Quinquecyclopropanol

Kurahashi, Takuya ; Kozhushkov, Sergei I ; Schill, Heiko ; Meindl, Kathrin ; Rühl, Stephan ; de Meijere, Armin

Angewandte Chemie (International ed.), 2007-01, Vol.46 (34), p.6545-6548 [Periódico revisado por pares]

Weinheim: Wiley-VCH Verlag

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5
1,10-Phenanthroline-H2O2-KSCN-CuSO4-NaOH oscillating chemiluminescence system
1,10-Phenanthroline-H2O2-KSCN-CuSO4-NaOH oscillating chemiluminescence system
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1,10-Phenanthroline-H2O2-KSCN-CuSO4-NaOH oscillating chemiluminescence system

Sorouraddin, M. H. ; Iranifam, M.

Luminescence (Chichester, England), 2009-03, Vol.24 (2), p.115-122 [Periódico revisado por pares]

Chichester, UK: John Wiley & Sons, Ltd

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6
1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols
1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols
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1,1,1-Tris(hydroxymethyl)ethane as a New, Efficient, and Versatile Tripod Ligand for Copper-Catalyzed Cross-Coupling Reactions of Aryl Iodides with Amides, Thiols, and Phenols

Chen, Yao-Jung ; Chen, Hsin-Hung

Organic letters, 2006-11, Vol.8 (24), p.5609-5612 [Periódico revisado por pares]

United States: American Chemical Society

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7
1,2 AND 1,4 ADDITIONS OF CINNAMIC ACID DERIVATIVES WITH SODIO KETONES, GRIGNARD REAGENTS, AND METALLIC AMIDES
1,2 AND 1,4 ADDITIONS OF CINNAMIC ACID DERIVATIVES WITH SODIO KETONES, GRIGNARD REAGENTS, AND METALLIC AMIDES
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1,2 AND 1,4 ADDITIONS OF CINNAMIC ACID DERIVATIVES WITH SODIO KETONES, GRIGNARD REAGENTS, AND METALLIC AMIDES

HAUSER, CHARLES R ; YOST, ROBERT S ; RINGLER, BETTY I

Journal of organic chemistry, 1949-03, Vol.14 (2), p.261-271 [Periódico revisado por pares]

United States: American Chemical Society

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8
1,2-bis(arylsulfonyl)hydrazines. 2. The influence of arylsulfonyl and aralkylsulfonyl substituents on antitumor and alkylating activity
1,2-bis(arylsulfonyl)hydrazines. 2. The influence of arylsulfonyl and aralkylsulfonyl substituents on antitumor and alkylating activity
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1,2-bis(arylsulfonyl)hydrazines. 2. The influence of arylsulfonyl and aralkylsulfonyl substituents on antitumor and alkylating activity

Shyam, K ; Furubayashi, R ; Hrubiec, R T ; Cosby, L A ; Sartorelli, A C

Journal of medicinal chemistry, 1986-07, Vol.29 (7), p.1323 [Periódico revisado por pares]

United States

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9
1,2-Di- O-acetyl-5- O-benzoyl-3-deoxy-3-fluoro- d-xylofuranose. A versatile precursor for the synthesis of 3-deoxy-3-fluoro-β- d-xylofuranosyl nucleosides as potential antiviral agents
1,2-Di- O-acetyl-5- O-benzoyl-3-deoxy-3-fluoro- d-xylofuranose. A versatile precursor for the synthesis of 3-deoxy-3-fluoro-β- d-xylofuranosyl nucleosides as potential antiviral agents
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1,2-Di- O-acetyl-5- O-benzoyl-3-deoxy-3-fluoro- d-xylofuranose. A versatile precursor for the synthesis of 3-deoxy-3-fluoro-β- d-xylofuranosyl nucleosides as potential antiviral agents

Gosselin, Gilles ; Puech, Frédéric ; Génu-Dellac, Corinne ; Imbach, Jean-Louis

Carbohydrate research, 1993-10, Vol.249 (1), p.1-17 [Periódico revisado por pares]

Netherlands: Elsevier Ltd

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10
1,2-Diacetylbenzene, the Neurotoxic Metabolite of a Chromogenic Aromatic Solvent, Induces Proximal Axonopathy
1,2-Diacetylbenzene, the Neurotoxic Metabolite of a Chromogenic Aromatic Solvent, Induces Proximal Axonopathy
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1,2-Diacetylbenzene, the Neurotoxic Metabolite of a Chromogenic Aromatic Solvent, Induces Proximal Axonopathy

Kim, Min-Sun ; Sabri, Mohammad I. ; Miller, Victor H. ; Kayton, Robert J. ; Dixon, David A. ; Spencer, Peter S.

Toxicology and applied pharmacology, 2001-12, Vol.177 (2), p.121-131 [Periódico revisado por pares]

San Diego, CA: Elsevier Inc

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