Cite
Enantioselective Michael addition of 2-nitropropane to chalcone analogues catalyzed by chiral azacrown ethers based on α-d-glucose and d-mannitol
MLA
Bakó, Tibor, et al. “Enantioselective Michael Addition of 2-Nitropropane to Chalcone Analogues Catalyzed by Chiral Azacrown Ethers Based on α-d-Glucose and d-Mannitol.” Tetrahedron: Asymmetry, vol. 14, no. 13, July 2003, p. 1917. EBSCOhost, https://doi.org/10.1016/S0957-4166(03)00351-3.
APA
Bakó, T., Bakó, P., Keglevich, G., Báthori, N., Czugler, M., Tatai, J., Novák, T., Parlagh, G., & Tőke, L. (2003). Enantioselective Michael addition of 2-nitropropane to chalcone analogues catalyzed by chiral azacrown ethers based on α-d-glucose and d-mannitol. Tetrahedron: Asymmetry, 14(13), 1917. https://doi.org/10.1016/S0957-4166(03)00351-3
Chicago
Bakó, Tibor, Péter Bakó, György Keglevich, Nikoletta Báthori, Mátyás Czugler, János Tatai, Tibor Novák, Gyula Parlagh, and László Tőke. 2003. “Enantioselective Michael Addition of 2-Nitropropane to Chalcone Analogues Catalyzed by Chiral Azacrown Ethers Based on α-d-Glucose and d-Mannitol.” Tetrahedron: Asymmetry 14 (13): 1917. doi:10.1016/S0957-4166(03)00351-3.