skip to main content
Idioma:
Primo Advanced Search
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search Query Term
Primo Advanced Search prefilters
Busca Simples
Resultados 1 2 3 4 5 next page
Mostrar Somente
Refinado por: assunto: Chemistry, Organic remover assunto: Preparations And Properties remover Physical Sciences remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts
Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts
Material Type:
Artigo 		Adicionar ao Meu Espaço

Synthesis of Azaheterocycles from Aryl Ketone O-Acetyl Oximes and Internal Alkynes by Cu–Rh Bimetallic Relay Catalysts

Too, Pei Chui ; Chua, Sze Hui ; Wong, Siong Heng ; Chiba, Shunsuke

Journal of organic chemistry, 2011-08, Vol.76 (15), p.6159-6168 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
2
A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions
A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions
Material Type:
Artigo 		Adicionar ao Meu Espaço

A β-Keto Ester as a Novel, Efficient, and Versatile Ligand for Copper(I)-Catalyzed C−N, C−O, and C−S Coupling Reactions

Lv, Xin ; Bao, Weiliang

Journal of organic chemistry, 2007-05, Vol.72 (10), p.3863-3867 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
3
Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization
Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization
Material Type:
Artigo 		Adicionar ao Meu Espaço

Construction of Nitrogen Heterocycles Bearing an Aminomethyl Group by Copper-Catalyzed Domino Three-Component Coupling−Cyclization

Ohta, Yusuke ; Chiba, Hiroaki ; Oishi, Shinya ; Fujii, Nobutaka ; Ohno, Hiroaki

Journal of organic chemistry, 2009-09, Vol.74 (18), p.7052-7058 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
4
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature
Material Type:
Artigo 		Adicionar ao Meu Espaço

TPGS-750-M: A Second-Generation Amphiphile for Metal-Catalyzed Cross-Couplings in Water at Room Temperature

Lipshutz, Bruce H ; Ghorai, Subir ; Abela, Alexander R ; Moser, Ralph ; Nishikata, Takashi ; Duplais, Christophe ; Krasovskiy, Arkady ; Gaston, Ricky D ; Gadwood, Robert C

Journal of organic chemistry, 2011-06, Vol.76 (11), p.4379-4391 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
5
Coupling Reactions of Heteroarenes with Phosphites under Silver Catalysis
Coupling Reactions of Heteroarenes with Phosphites under Silver Catalysis
Material Type:
Artigo 		Adicionar ao Meu Espaço

Coupling Reactions of Heteroarenes with Phosphites under Silver Catalysis

Xiang, Chang-Bing ; Bian, Yong-Jun ; Mao, Xue-Rong ; Huang, Zhi-Zhen

Journal of organic chemistry, 2012-09, Vol.77 (17), p.7706-7710 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
6
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway
Material Type:
Artigo 		Adicionar ao Meu Espaço

Mechanistic Studies on the Cu-Catalyzed Three-Component Reactions of Sulfonyl Azides, 1-Alkynes and Amines, Alcohols, or Water: Dichotomy via a Common Pathway

Yoo, Eun Jeong ; Ahlquist, Mårten ; Bae, Imhyuck ; Sharpless, K. Barry ; Fokin, Valery V ; Chang, Sukbok

Journal of organic chemistry, 2008-07, Vol.73 (14), p.5520-5528 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
7
Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process
Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process
Material Type:
Artigo 		Adicionar ao Meu Espaço

Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process

Cano, Rafael ; Ramón, Diego J ; Yus, Miguel

Journal of organic chemistry, 2011-07, Vol.76 (14), p.5547-5557 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
8
Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles
Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles
Material Type:
Artigo 		Adicionar ao Meu Espaço

Exploring Catalyst and Solvent Effects in the Multicomponent Synthesis of Pyridine-3,5-dicarbonitriles

Guo, Kai ; Thompson, Mark J ; Chen, Beining

Journal of organic chemistry, 2009-09, Vol.74 (18), p.6999-7006 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
9
CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism
CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism
Material Type:
Artigo 		Adicionar ao Meu Espaço

CuO Nanoparticles Catalyzed C−N, C−O, and C−S Cross-Coupling Reactions: Scope and Mechanism

Jammi, Suribabu ; Sakthivel, Sekarpandi ; Rout, Laxmidhar ; Mukherjee, Tathagata ; Mandal, Santu ; Mitra, Raja ; Saha, Prasenjit ; Punniyamurthy, Tharmalingam

Journal of organic chemistry, 2009-03, Vol.74 (5), p.1971-1976 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
10
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos
Material Type:
Artigo 		Adicionar ao Meu Espaço

Palladium-Catalyzed Carbonylation Reactions of Aryl Bromides at Atmospheric Pressure: A General System Based on Xantphos

Martinelli, Joseph R ; Watson, Donald A ; Freckmann, Dominique M. M ; Barder, Timothy E ; Buchwald, Stephen L

Journal of organic chemistry, 2008-09, Vol.73 (18), p.7102-7107 [Periódico revisado por pares]

Washington, DC: American Chemical Society

Texto completo disponível

Citações Citado por
Resultados 1 2 3 4 5 next page

Personalize Seus Resultados

  1. Editar

Refine Search Results

Expandir Meus Resultados

  1.   

Mostrar Somente

  1. Recursos Online (57.749)
  2. Revistas revisadas por pares (58.359)

Refinar Meus Resultados

Tipo de Recurso 

  1. Artigos  (58.558)
  2. Resenhas  (17)
  3. Anais de Congresso  (3)
  4. Book Chapters  (1)
  5. Mais opções open sub menu

Data de Publicação 

De até
Refinar
  1. Antes de1987  (9.170)
  2. 1987Até1992  (19.232)
  3. 1993Até1998  (8.423)
  4. 1999Até2005  (4.595)
  5. Após 2005  (17.160)
  6. Mais opções open sub menu

Idioma 

  1. Japonês  (12.099)
  2. Alemão  (17)
  3. Francês  (7)
  4. Galês  (1)
  5. Mais opções open sub menu

  • Realização: ABCD-USP USP   Logos de Redes Sociais: Freepik

Buscando em bases de dados remotas. Favor aguardar.