Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide (2003)
- Authors:
- USP affiliated authors: POLITI, MARIO JOSE - IQ ; CUCCOVIA, IOLANDA MIDEA - IQ ; GURALNIK, HERNAN CHAIMOVICH - IQ ; BERCI FILHO, PEDRO - IQSC
- Unidades: IQ; IQSC
- DOI: 10.1002/poc.618
- Assunto: FÍSICO-QUÍMICA ORGÂNICA
- Language: Inglês
- Imprenta:
- Publisher place: Chichester
- Date published: 2003
- Source:
- Título: Journal of Physical Organic Chemistry
- ISSN: 0894-3230
- Volume/Número/Paginação/Ano: v. 16, p. 311-317, 2003
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
TRIBONI, Eduardo Rezende et al. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide. Journal of Physical Organic Chemistry, v. 16, p. 311-317, 2003Tradução . . Disponível em: https://doi.org/10.1002/poc.618. Acesso em: 28 dez. 2025. -
APA
Triboni, E. R., Politi, M. J., Cuccovia, I. M., Chaimovich Guralnik, H., & Berci Filho, P. (2003). Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide. Journal of Physical Organic Chemistry, 16, 311-317. doi:10.1002/poc.618 -
NLM
Triboni ER, Politi MJ, Cuccovia IM, Chaimovich Guralnik H, Berci Filho P. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide [Internet]. Journal of Physical Organic Chemistry. 2003 ; 16 311-317.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1002/poc.618 -
Vancouver
Triboni ER, Politi MJ, Cuccovia IM, Chaimovich Guralnik H, Berci Filho P. Rate-limiting step and micellar catalysis of the non-classical nitro group nucleophilic substitution by thiols in 4-nitro-N-n-butyl-1,8-naphthalimide [Internet]. Journal of Physical Organic Chemistry. 2003 ; 16 311-317.[citado 2025 dez. 28 ] Available from: https://doi.org/10.1002/poc.618 - Neighboring group participation in the formation and decomposition of amides
- Formacao e decomposicao de n-alquilimidas e anidridos derivados dos acidos 2,3 e 1,8-naftalicos
- Reactions of N-alkylnaphthalimides: towards artificial proteases
- Formation and decomposition of N-alkylnaphthalimides: experimental evidences and ab initio description of the reaction pathways
- Aromatic nitro substitution reaction between 4-nitro-N-n-butyl-1,8-naphthalimide and n-heptanethiol in water-methanol binary mixtures
- Hydrolysis of 1,8-and 2,3-naphthalic anhydrides and the mechanism of cyclization of 1,8-naphthalic acid in aqueous solutions
- Vesicles in catalysis
- Catalysis and inhibition by micelles and vesicles
- Micellar effects on reaction mechanisms
- Weight - averaged molecular weight by light scattering of chloroform injected dodac vesicles
Informações sobre o DOI: 10.1002/poc.618 (Fonte: oaDOI API)
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