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1
Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition
Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition
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Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition

Hélio Alexandre Stefani Hugo A Canduzini; Flávia Manarin

Tetrahedron Letters Oxford v. 52, n. 46, p. 6086-6090 : + Supplementary materials (p. S1-S10), 2011

Oxford 2011

Item não circula. Consulte sua biblioteca.(Acessar)

2
Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition
Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition
Material Type:
Artigo 		Adicionar ao Meu Espaço

Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition

Hélio Alexandre Stefani Hugo A Canduzini; Flávia Manarin

Tetrahedron Letters Oxford v. 52, n. 46, p. 6086-6090 : + Supplementary materials (p. S1-S10), 2011

Oxford 2011

Item não circula. Consulte sua biblioteca.(Acessar)

3
Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters efficient synthesis of β-unsaturated α-amino esters
Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters efficient synthesis of β-unsaturated α-amino esters
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Ytterbium(III)-catalyzed addition reaction of alkynyltrifluoroborate salts to α-imino esters efficient synthesis of β-unsaturated α-amino esters

Hélio Alexandre Stefani Flávia Manarin; Amna N Khan; Stanley Nunes Siqueira Vasconcelos

European Journal of Organic Chemistry Weinheim v. 6, p. 1236-1240, 2014

Weinheim 2014

Item não circula. Consulte sua biblioteca.(Acessar)

4
Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters
Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters
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Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters

Hélio Alexandre Stefani Flávia Manarin; Ariane C.S Sousa; Frederico B Souza; Witor Ribeiro Ferraz

Tetrahedron Oxford v. 70, n. 20, p. 3243-3248, 2014

Oxford 2014

Item não circula. Consulte sua biblioteca.(Acessar)

5
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction
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Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction

Hélio Alexandre Stefani Nathália Cristina da Silva e Silva; Stanley Nunes Siqueira Vasconcelos; Flávia Manarin; Frederico B Souza

Tetrahedron Letters Oxford v. 54, n. 22, p. 2809-2812, 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

6
One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles
One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles
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One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles

Hélio Alexandre Stefani Stanley Nunes Siqueira Vasconcelos; Frederico B Souza; Flávia Manarin; Júlio Zukerman-Schpector

Tetrahedron Letters Oxford v. 54, n. 43, p. 5821-5825, 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

7
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction
Material Type:
Artigo 		Adicionar ao Meu Espaço

Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction

Hélio Alexandre Stefani Nathália Cristina da Silva e Silva; Stanley Nunes Siqueira Vasconcelos; Flávia Manarin; Frederico B Souza

Tetrahedron Letters Oxford v. 54, n. 22, p. 2809-2812, 2013

Oxford 2013

Item não circula. Consulte sua biblioteca.(Acessar)

8
Negishi cross-coupling of organotellurium compounds synthesis of biaryls, aryl-, and diaryl acetylenes
Negishi cross-coupling of organotellurium compounds synthesis of biaryls, aryl-, and diaryl acetylenes
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Negishi cross-coupling of organotellurium compounds synthesis of biaryls, aryl-, and diaryl acetylenes

Hélio Alexandre Stefani Jesus Marcelo Pena; Flávia Manarin; Rômulo Augusto Ando; Daiana Mendes Leal; Nicola Petragnani

Tetrahedrn Letters Oxford v. 52, n. 34, p. 4398-4401 : + Supplementary materials (p. S1-S9), 2011

Oxford 2011

Item não circula. Consulte sua biblioteca.(Acessar)

9
Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´
Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´
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Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´

Hélio Alexandre Stefani AMNA N Khan; Flávia Manarin; Pedro H Vendramini; Marcos Nogueira Eberlin

Tetrahedron Letters Basel v. 54, n. 46, p. 6204-6207, 2013

Basel 2013

Item não circula. Consulte sua biblioteca.(Acessar)

10
Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling
Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling
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Copper(I)/succinic acid cooperatively catalyzed one-pot synthesis of organoseleniumpropargylamines via 'A POT. 3' -coupling

Isadora Maria de Oliveira Daniel Carvalho Pimenta; Júlio Zukerman-Schpector; Hélio Alexandre Stefani; Flávia Manarin

New Journal of Chemistry Cambridge v. 42, n. 12, p. 10118-10123, 2018

Cambridge 2018

Item não circula. Consulte sua biblioteca.(Acessar)

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Deste Autor:

  1. Stefani, H
  2. Manarin, F
  3. Oliveira, I
  4. Monteiro, F
  5. Manarin, S

Neste Assunto:

  1. Síntese Orgânica
  2. Science & Technology
  3. Itérbio
  4. Telúrio
  5. Capim Mombaça

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

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