skip to main content
Resultados 1 2 3 next page
Refinado por: Nome da Publicação: Cheminform remover
Result Number Material Type Add to My Shelf Action Record Details and Options
1
ChemInform Abstract: Regiocontrolled SNAr Reaction on 2,3-Dihalopyridines with NaSMe to Obtain Bromo(methylthio)pyridines as Key Precursors of 3-Halo-2-(hetero)arylthieno[2,3-b]pyridines and Thieno[3,2-b]pyridines
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Regiocontrolled SNAr Reaction on 2,3-Dihalopyridines with NaSMe to Obtain Bromo(methylthio)pyridines as Key Precursors of 3-Halo-2-(hetero)arylthieno[2,3-b]pyridines and Thieno[3,2-b]pyridines

Begouin, Agathe ; Peixoto, Daniela ; Queiroz, Maria-Joao R. P.

ChemInform, 2013-09, Vol.44 (39), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

2
ChemInform Abstract: Scope and Limitations of the Base-Free Copper(I) Oxide Catalyzed N-Heteroarylation of 1H-(Benz)imidazoles with B-Heteroarylboronic Acids or 2-Heteroaryl-4,4,5,5-tetramethyl-1,3,2-dioxaborolanes
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Scope and Limitations of the Base-Free Copper(I) Oxide Catalyzed N-Heteroarylation of 1H-(Benz)imidazoles with B-Heteroarylboronic Acids or 2-Heteroaryl-4,4,5,5-tetramethyl-1,3,2-dioxaborolanes

Begouin, Agathe ; Queiroz, Maria-Joao R. P.

ChemInform, 2013-09, Vol.44 (39), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

3
ChemInform Abstract: New Di(hetero)arylethers and Di(hetero)arylamines in the Thieno[3,2-b]pyridine Series: Synthesis, Growth Inhibitory Activity on Human Tumor Cell Lines and Non-tumor Cells, Effects on Cell Cycle and on Programmed Cell Death
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: New Di(hetero)arylethers and Di(hetero)arylamines in the Thieno[3,2-b]pyridine Series: Synthesis, Growth Inhibitory Activity on Human Tumor Cell Lines and Non-tumor Cells, Effects on Cell Cycle and on Programmed Cell Death

Queiroz, Maria-Joao R. P. ; ., et al

ChemInform, 2014-04, Vol.45 (15), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

4
ChemInform Abstract: Synthesis of 2-(Hetero)arylthieno[2,3-b] or [3,2-b]Pyridines from 2,3-Dihalopyridines, (Hetero)arylalkynes, and Na2S. Further Functionalizations
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Synthesis of 2-(Hetero)arylthieno[2,3-b] or [3,2-b]Pyridines from 2,3-Dihalopyridines, (Hetero)arylalkynes, and Na2S. Further Functionalizations

Peixoto, Daniela ; Begouin, Agathe ; Queiroz, Maria-Joao R. P.

ChemInform, 2013-01, Vol.44 (1), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

5
ChemInform Abstract: Tandem Palladium/Charcoal-Copper(I) Iodide (Pd/C-CuI) Catalyzed Sonogashira Coupling and Intramolecular Cyclization from 2-Bromonicotinic Acid (= 2-Bromopyridine-3-carboxylic Acid) and Ethynylarenes to 4-Azaphthalides (= Furo[3,4-b]pyridin-5(7H)-ones) and 5-Azaisocoumarins (= 5H-Pyrano[4,3-b]pyridin-5-ones)
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Tandem Palladium/Charcoal-Copper(I) Iodide (Pd/C-CuI) Catalyzed Sonogashira Coupling and Intramolecular Cyclization from 2-Bromonicotinic Acid (= 2-Bromopyridine-3-carboxylic Acid) and Ethynylarenes to 4-Azaphthalides (= Furo[3,4-b]pyridin-5(7H)-ones) and 5-Azaisocoumarins (= 5H-Pyrano[4,3-b]pyridin-5-ones)

Begouin, Agathe ; Queiroz, Maria-Joao R. P.

ChemInform, 2012-02, Vol.43 (8), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

6
Synthesis of Diarylamines in the Thiophene Series by Buchwald-Hartwig Coupling
Material Type:
Artigo
Adicionar ao Meu Espaço

Synthesis of Diarylamines in the Thiophene Series by Buchwald-Hartwig Coupling

Begouin, Agathe ; Hesse, Stephanie ; Queiroz, Maria-Joao R. P. ; Kirsch, Gilbert

ChemInform, 2006-01, Vol.37 (4), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

7
ChemInform Abstract: Synthesis of New Thieno[3,2-b]pyridine Derivatives by Palladium-Catalyzed Couplings and Intramolecular Cyclizations
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Synthesis of New Thieno[3,2-b]pyridine Derivatives by Palladium-Catalyzed Couplings and Intramolecular Cyclizations

Calhelha, Ricardo C. ; Queiroz, Maria-Joao R. P.

ChemInform, 2010-04, Vol.41 (17), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

8
ChemInform Abstract: Palladium-Catalyzed Multicomponent Aminocarbonylation of Aryl or Heteroaryl Halides with [Mo(CO)6] and Aryl- or Heteroarylamines Using Conventional Heating
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Palladium-Catalyzed Multicomponent Aminocarbonylation of Aryl or Heteroaryl Halides with [Mo(CO)6] and Aryl- or Heteroarylamines Using Conventional Heating

Begouin, Agathe ; Queiroz, Maria-Joao R. P.

ChemInform, 2009-10, Vol.40 (42), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

9
ChemInform Abstract: Reactivity of Several Deactivated 3-Aminobenzo[b]thiophenes in the Buchwald-Hartwig C-N Coupling. Scope and Limitations
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: Reactivity of Several Deactivated 3-Aminobenzo[b]thiophenes in the Buchwald-Hartwig C-N Coupling. Scope and Limitations

Queiroz, Maria-Joao R. P. ; Calhelha, Ricardo C. ; Kirsch, Gilbert

ChemInform, 2008-05, Vol.39 (21), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

10
ChemInform Abstract: New Synthesis of Methyl 5-Aryl or Heteroaryl Pyrrole-2-carboxylates by a Tandem Sonogashira Coupling/5-endo-dig-Cyclization from β-Iododehydroamino Acid Methyl Esters and Terminal Alkynes
Material Type:
Artigo
Adicionar ao Meu Espaço

ChemInform Abstract: New Synthesis of Methyl 5-Aryl or Heteroaryl Pyrrole-2-carboxylates by a Tandem Sonogashira Coupling/5-endo-dig-Cyclization from β-Iododehydroamino Acid Methyl Esters and Terminal Alkynes

Queiroz, Maria-Joao R. P. ; Begouin, Agathe ; Pereira, Goreti ; Ferreira, Paula M. T.

ChemInform, 2009-03, Vol.40 (12), p.no-no

Weinheim: WILEY-VCH Verlag

Texto completo disponível

Resultados 1 2 3 next page

Buscando em bases de dados remotas. Favor aguardar.