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1
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoquinodimethane ( tcnq ) in organic solvents
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoquinodimethane ( tcnq ) in organic solvents
Material Type:
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Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoquinodimethane ( tcnq ) in organic solvents

Omar A El Seoud F P Ribeiro; A Martins; P P Brotero

Washington v.50, p.5099-102, 1985 Journal of Organic Chemistry

Washington 1985

Item não circula. Consulte sua biblioteca.(Acessar)

2
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents

Omar A El Seoud F P Ribeiro; A Martins; P P Brotero

Washington v.50, n.25, p.5099-102, 1985 Journal of Organic Chemistry

Washington 1985

Item não circula. Consulte sua biblioteca.(Acessar)

3
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents
Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents
Material Type:
Artigo 		Adicionar ao Meu Espaço

Kinetics of the reaction of alkylamines with 7,7,8,8- tetracyanoguinodimethane (tcnq) in organic solvents

Omar A El Seoud F P Ribeiro; A Martins; P P Brotero

Washington v.50, n.25, p.5099-102, 1985 Journal of Organic Chemistry

Washington 1985

Item não circula. Consulte sua biblioteca.(Acessar)

4
Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation
Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation
Material Type:
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Copper-catalyzed synthesis of pyrrolo[1,2-c]quinazolines and pyrrolo[2,1-a]isoquinolines and antiplasmodial evaluation

Natália Menezes Moreira Ingrid Telles de Miranda; Jhonathan Renner Nunes dos Santos; Till Opatz; Glaucius Oliva; Rafael Victorio Carvalho Guido; Arlene Gonçalves Corrêa

Journal of Organic Chemistry Washington, DC v. 88, n. 13, p. 8781-8790 + supporting information: 1-30, July 2023

Washington, DC 2023

Localização: IFSC - Inst. Física de São Carlos    (PROD034663 )(Acessar)

5
Intramolecular electronic and hydrogen-bonding interactions in N.N-Dimethyl-2,3-di-O-methyl-L-tartaramide
Intramolecular electronic and hydrogen-bonding interactions in N.N-Dimethyl-2,3-di-O-methyl-L-tartaramide
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Intramolecular electronic and hydrogen-bonding interactions in N.N-Dimethyl-2,3-di-O-methyl-L-tartaramide

Carlos Alemán Sérgio Emanuel Galembeck

Journal of Organic Chemistry Baltimore

Baltimore 1997

Item não circula. Consulte sua biblioteca.(Acessar)

6
Hydrozirconation of stannylacetylenes synthesis and reactions of ketene stannyl (Telluro) acetals
Hydrozirconation of stannylacetylenes synthesis and reactions of ketene stannyl (Telluro) acetals
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Hydrozirconation of stannylacetylenes synthesis and reactions of ketene stannyl (Telluro) acetals

Miguel Joaquim Dabdoub Adriano Cesar de Morais Baroni

Journal of Organic Chemistry Washigton v. 65, n. 1, p. 54-60, 2000

Washington 2000

Localização: FFCLRP - Fac. Fil. Ciên. Let. de R. Preto    (pcd 1127517 )(Acessar)

7
Hydrozirconation of lithium alkynylselenolate anions generation and reactions of 'alfa'-zirconated vinyl selenide intermediates
Hydrozirconation of lithium alkynylselenolate anions generation and reactions of 'alfa'-zirconated vinyl selenide intermediates
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Hydrozirconation of lithium alkynylselenolate anions generation and reactions of 'alfa'-zirconated vinyl selenide intermediates

Miguel Joaquim Dabdoub Mauro Luiz Begnini; Palimécio G Guerrero; Adriano Cesar de Morais Baroni

Journal of Organic Chemistry Washington v. 65, n. 1, p. 61-67, 2000

washington 2000

Localização: FFCLRP - Fac. Fil. Ciên. Let. de R. Preto    (pcd 1127116 )(Acessar)

8
Thallium trinitrate mediated ring contraction of trans-2-decalones an alternative entry to the hydrindane system
Thallium trinitrate mediated ring contraction of trans-2-decalones an alternative entry to the hydrindane system
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Thallium trinitrate mediated ring contraction of trans-2-decalones an alternative entry to the hydrindane system

Helena Maria Carvalho Ferraz L F Silva Junior

Journal of Organic Chemistry Washington v. 63, p. 1716-9, 1998

Washington 1998

Item não circula. Consulte sua biblioteca.(Acessar)

9
Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone Efficient kinetic resolution of chiral racemic vinylcyclohexenes
Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone Efficient kinetic resolution of chiral racemic vinylcyclohexenes
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Enantioselective Diels-Alder cycloadditions with (SS)-2-(p-tolylsulfinyl)-1,4-naphthoquinone Efficient kinetic resolution of chiral racemic vinylcyclohexenes

M C Carreño Antonio Urbano; Cláudio Di Vitta

Journal of Organic Chemistry Washington v. 63, n. 23, p. 8320-8330, 1998

Washington 1998

Item não circula. Consulte sua biblioteca.(Acessar)

10
Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran the chemical Modifications drive the pseudoratational preferences
Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran the chemical Modifications drive the pseudoratational preferences
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Conformational preferences of 2,3,3a,8a-Tetrahydrofuro[2,3-b]benzofuran the chemical Modifications drive the pseudoratational preferences

Carlos Alemán Paulo Marcos Donate; Rosangela da Silva; Gil Valdo José da Silva

Journal of Organic Chemistry Columbus v. 65, p. 5712-5714, 1999

Columbus 1999

Localização: FFCLRP - Fac. Fil. Ciên. Let. de R. Preto    (pcd 1075685 )(Acessar)

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Deste Autor:

  1. Ferraz, H
  2. Galembeck, S
  3. Constantino, M
  4. Oliveira, K
  5. El Seoud, O

Neste Assunto:

  1. Química Orgânica
  2. Síntese Orgânica
  3. Reações Orgânicas
  4. Solvente
  5. Química

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

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