A theoretical investigation of the dictating forces in small amino acid conformational preferences: the case of glycine, sarcosine and N,N-dimethylglycine (2013)
- Authors:
- Autor USP: DUCATI, LUCAS COLUCCI - IQ
- Unidade: IQ
- DOI: 10.1016/j.chemphys.2013.05.007
- Subjects: AMINOÁCIDOS; ESTEREOQUÍMICA
- Language: Inglês
- Imprenta:
- Source:
- Título: Chemical Physics
- ISSN: 0301-0104
- Volume/Número/Paginação/Ano: v. 421, p. 32-38, 2013
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
CORMANICH, Rodrigo Antônio et al. A theoretical investigation of the dictating forces in small amino acid conformational preferences: the case of glycine, sarcosine and N,N-dimethylglycine. Chemical Physics, v. 421, p. 32-38, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.chemphys.2013.05.007. Acesso em: 13 fev. 2026. -
APA
Cormanich, R. A., Ducati, L. C., Tormena, C. F., & Rittner, R. (2013). A theoretical investigation of the dictating forces in small amino acid conformational preferences: the case of glycine, sarcosine and N,N-dimethylglycine. Chemical Physics, 421, 32-38. doi:10.1016/j.chemphys.2013.05.007 -
NLM
Cormanich RA, Ducati LC, Tormena CF, Rittner R. A theoretical investigation of the dictating forces in small amino acid conformational preferences: the case of glycine, sarcosine and N,N-dimethylglycine [Internet]. Chemical Physics. 2013 ; 421 32-38.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1016/j.chemphys.2013.05.007 -
Vancouver
Cormanich RA, Ducati LC, Tormena CF, Rittner R. A theoretical investigation of the dictating forces in small amino acid conformational preferences: the case of glycine, sarcosine and N,N-dimethylglycine [Internet]. Chemical Physics. 2013 ; 421 32-38.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1016/j.chemphys.2013.05.007 - The unexpected roles of sigma and pi orbitals in electron donor and acceptor group effects on the C-13 NMR chemical shifts in substituted benzenest
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Informações sobre o DOI: 10.1016/j.chemphys.2013.05.007 (Fonte: oaDOI API)
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