Source: Journal of Molecular Structure. Unidade: IFSC
Assunto: CRISTALOGRAFIA
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SEIDL, P. R. et al. Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure. Journal of Molecular Structure, v. 654, p. 139-143, 2003Tradução . . Disponível em: https://doi.org/10.1016/s0022-2860(03)00204-7. Acesso em: 22 jun. 2024.APA
Seidl, P. R., Sabino, J. R., Castellano, E. E., Mascarenhas, Y. P., Costa, V. E. U., Alifantes, J., et al. (2003). Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure. Journal of Molecular Structure, 654, 139-143. doi:10.1016/s0022-2860(03)00204-7NLM
Seidl PR, Sabino JR, Castellano EE, Mascarenhas YP, Costa VEU, Alifantes J, Paula e Silva CHT, Dias JF. Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure [Internet]. Journal of Molecular Structure. 2003 ; 654 139-143.[citado 2024 jun. 22 ] Available from: https://doi.org/10.1016/s0022-2860(03)00204-7Vancouver
Seidl PR, Sabino JR, Castellano EE, Mascarenhas YP, Costa VEU, Alifantes J, Paula e Silva CHT, Dias JF. Co-crystallization of pentacyclododecane acetate rotamers of opposite chirality: effects of steric interactions and negative hyperconjugation on molecular structure [Internet]. Journal of Molecular Structure. 2003 ; 654 139-143.[citado 2024 jun. 22 ] Available from: https://doi.org/10.1016/s0022-2860(03)00204-7
