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1
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids
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Artigo 		Adicionar ao Meu Espaço

Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids

Hélio Alexandre Stefani Monica Franco Zanini Junqueira Amaral; Gloria Reyes-Rangel; Jorge Vargas-Caporali; Eusebio Juaristi

European Journal of Organic Chemistry Weinheim v. 2010, n. 33, p. 6393-6403, 2010

Weinheim 2010

Item não circula. Consulte sua biblioteca.(Acessar)

2
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals
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α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals

Mariana P Darbem Henrique A Esteves; Isadora Maria de Oliveira; Hélio Alexandre Stefani

European Journal of Organic Chemistry Weinheim v. 2020, p. 5220–5226, 2020

Weinheim 2020

Item não circula. Consulte sua biblioteca.(Acessar)

3
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids
Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids
Material Type:
Artigo 		Adicionar ao Meu Espaço

Functionalization of (2S)-isopropyl-5-iodo-2,3-dihydro-4(H)-pyrimidin-4-ones by a Suzuki-Miyaura cross-coupling reaction using aryltrifluoroborate salts convenient enantioselective preparation of 'alpha'-substituted 'beta'-amino acids

Hélio Alexandre Stefani Monica Franco Zanini Junqueira Amaral; Gloria Reyes-Rangel; Jorge Vargas-Caporali; Eusebio Juaristi

European Journal of Organic Chemistry Weinheim v. 2010, n. 33, p. 6393-6403, 2010

Weinheim 2010

Item não circula. Consulte sua biblioteca.(Acessar)

4
Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides
Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides
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Carbonylative negishi-type coupling of 2-iodoglycals with alkyl and aryl halides

Henrique A Esteves Mariana P Darbem; Daniel Carvalho Pimenta; Hélio Alexandre Stefani

European Journal of Organic Chemistry Weinheim v. 2019, p. 7384-7388, 2019

Weinheim 2019

Item não circula. Consulte sua biblioteca.(Acessar)

5
Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals
Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals
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Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals

Antonio Augusto Soares Paulino Hélio Alexandre Stefani

European Journal of Organic Chemistry Weinhein v. 2020, p. 3847–3855, 2020

Weinhein 2020

Item não circula. Consulte sua biblioteca.(Acessar)

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Assunto 

  1. Aminoácidos  (2)
  2. Ureia  (1)
  3. Monóxido De Carbono  (1)
  4. Glicosídeos  (1)
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Deste Autor:

  1. Stefani, H
  2. Darbem, M
  3. Esteves, H
  4. Vargas-Caporali, J
  5. Juaristi, E

Neste Assunto:

  1. Paládio
  2. Aminoácidos
  3. Ureia
  4. Monóxido De Carbono
  5. Glicosídeos

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

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