An explanation about the use of (S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1H and 13C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: a theoretical-experimental study (2019)
- Authors:
- USP affiliated authors: PALARETTI, VINICIUS - FFCLRP ; DIAS, LUIS GUSTAVO - FFCLRP ; SILVA, GIL VALDO JOSE DA - FFCLRP ; TAKAHASHI, VIVIANI NARDINI - FFCLRP
- Unidade: FFCLRP
- DOI: 10.3390/molecules24152830
- Subjects: ALDEÍDOS; QUÍMICA TEÓRICA; ESPECTROSCOPIA DE RESSONÂNCIA MAGNÉTICA NUCLEAR; ORBITAL MOLECULAR
- Keywords: Long-chain imine; Conformation; NMR; NOE
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Este periódico é de acesso aberto
- Este artigo é de acesso aberto
- URL de acesso aberto
- Cor do Acesso Aberto: gold
- Licença: cc-by
-
ABNT
TAKAHASHI, Viviani Nardini et al. An explanation about the use of (S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1H and 13C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: a theoretical-experimental study. Molecules, v. 24, n. 15, p. [11] , 2019Tradução . . Disponível em: https://doi.org/10.3390/molecules24152830. Acesso em: 29 dez. 2025. -
APA
Takahashi, V. N., Palaretti, V., Dias, L. G., & Silva, G. V. J. da. (2019). An explanation about the use of (S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1H and 13C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: a theoretical-experimental study. Molecules, 24( 15), [11] . doi:10.3390/molecules24152830 -
NLM
Takahashi VN, Palaretti V, Dias LG, Silva GVJ da. An explanation about the use of (S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1H and 13C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: a theoretical-experimental study [Internet]. Molecules. 2019 ; 24( 15): [11] .[citado 2025 dez. 29 ] Available from: https://doi.org/10.3390/molecules24152830 -
Vancouver
Takahashi VN, Palaretti V, Dias LG, Silva GVJ da. An explanation about the use of (S)-Citronellal as a Chiral Derivatizing Agent (CDA) in 1H and 13C NMR for Sec-Butylamine, Methylbenzylamine, and Amphetamine: a theoretical-experimental study [Internet]. Molecules. 2019 ; 24( 15): [11] .[citado 2025 dez. 29 ] Available from: https://doi.org/10.3390/molecules24152830 - Studies towards rotational dynamics of dimethyl 2-(triphenylphosphoranylidene) succinate by 1H NMR
- Preparação de intermediários para a síntese de furano-heliangolidos
- Synthesis and dopamine receptor binding of dihydrexidine and SKF 38393 catecholamine-based analogues
- Stereochemical assignment of four diastereoisomers of a maculalactone derivative by computational NMR calculations
- Cerium metal-mediated reformatsky-type reaction with ethyl bromosuccinate for the synthesis of novel paraconic acid analogs
- Assignment of NMR data and relative stereochemistry determination of paraconic acid derivatives
- Side-chain modifications of highly functionalized 3(2H0)-furanones
- Determinação do excesso enantiomérico e configuração absoluta de aminas quirais por rossonância magnética nuclear (RMN)
- Estudos sobre a síntese de furanoeliangolidos
- Investigação das propriedades catalíticas de metaloporfirinas e complexos salen na oxidação do agente antimicrobiano clorexidina
Informações sobre o DOI: 10.3390/molecules24152830 (Fonte: oaDOI API)
Download do texto completo
| Tipo | Nome | Link | |
|---|---|---|---|
 |
002974302.pdf | Direct link |
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
