Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases (2021)
- Authors:
- USP affiliated authors: LOURENÇO, RICARDO VESSECCHI - FFCLRP ; CLOSOSKI, GIULIANO CESAR - FCFRP ; SANTOS, THIAGO DOS - FCFRP ; ORENHA, HENRIQUE PEREIRA - FCFRP ; MURIE, VALTER EDUARDO - FCFRP
- Unidades: FFCLRP; FCFRP
- DOI: 10.1021/acs.orglett.1c02572
- Subjects: COMPOSTOS DE NITROGÊNIO; NITRILAS; QUÍMICA ORGÂNICA; COMPOSTOS HETEROCÍCLICOS
- Keywords: Cross coupling reaction; Electrophiles; Functionalization; Metalation; Nitrogen compounds
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Washington
- Date published: 2021
- Source:
- Título do periódico: Organic Letters
- ISSN: 1523-7060
- Volume/Número/Paginação/Ano: v. 23, n. 19, p. 7396-7400, 2021
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 29 maio 2024. -
APA
Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572 -
NLM
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 maio 29 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572 -
Vancouver
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2024 maio 29 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572 - Regioselective functionalization of ester-, amide-, carbonate-, and carbamate-substituted 2-phenyl-2-oxazolines with mixed lithium–magnesium amides
- Síntese de novos derivados triazólicos do eugenol de interesse medicinal
- Selective functionalization of benzo‐fused N‐heterocycles by using in situ trapping metalations
- Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
- Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl
- Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl
- Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones
- Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization
- Directed functionalization of cyano-substituted furans and thiophenes with TMPMgCl•LiCl
- Base-controlled regioselective functionalization of chloro-substituted quinolines
Informações sobre o DOI: 10.1021/acs.orglett.1c02572 (Fonte: oaDOI API)
Download do texto completo
Tipo | Nome | Link | |
---|---|---|---|
003088718.pdf |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas