| Referências: |
BIBLIOGRAFIA:
BÁSICA:
• Eliel, E. L.; Wilen, S. H. Stereochemistry of Organic Compounds. John Wiley & Sons, New York, 1994.
• Jacobsen, E.N.; Pfaltz, A.; Yamamoto, H. Comprehensive Asymmetric Catalysis I–III. Rev. Edition. Springer, 2003.
• Karnik, A.V.; Hasan, M. Stereochemistry: a three-dimensional insight. 1st edition. Elsevier, 2021.
• Krupadanam, G.L.D. Fundamentals of Asymmetric Synthesis. 1st edition. CRC Press, 2014.
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• Morrison, J.D. Asymmetric Synthesis Volume 1: Analytical Methods. 1st edition. Academic Press, 1983.
COMPLEMENTAR:
• Francotte, E.; Lindner, W. Chirality in Drug Research. 1st edition. Wiley, 2006.
• Gridnev, I.D.; Dub, P.A. Enantioselection in Asymmetric Catalysis. 1st edition. CRC Press, 2019.
• Reddy, I.K.; Mehvar, R. Chirality in Drug Design and Development. 1st edition. CRC Press, 2004.
• Yang, J. Six-membered Transition States in Organic Synthesis. 1st edition. Wiley-Interscience, 2010.
• Zhu, H. Organic Stereochemistry: Experimental and Computational Methods. 1st edition. Wiley, 2015.
PERÍODICOS CIENTÍFICOS E OUTROS:
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• Fance, S.; Guerin, D. J.; Miller, S. J.; Leckta, T., Nucleophilic Chiral Amines as Catalysts in Asymmetric Synthesis. Chem Rev. 2003, 103, 2985.
• Finelli, F.G.; Santos, B.; Frota, L. Organocatálise enantiosseletiva: evolução e aspectos recentes. Química Nova. 2019, 42, 425.
• Hajos, Z.G.; Parrish, D.R. Asymmetric synthesis of bicyclic intermediates of natural product chemistry. J. Org. Chem. 1974, 39, 1615.
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• Kobayashi, S.; Ishitani, H. Catalytic enantioselective addition to imines. Chem. Rev. 1999, 99, 1069.
• Lourenço, T.C.; Cassiano, N.M.; Cass, Q.B. Fases Estacionárias para Cromatografia Líquida de Alta Eficiência. Química Nova. 2010, 33, 10, 2155.
• Martins, B.S.; Lüdke, D.S.; Moro, A.V. Modelos Estereoquímicos de Adição à Carbonila. Química Nova. 2017, 40, 3, 342.
• Mukherjee, S.; Yang, J.W.; Hoffmann, S.; List, B. Asymmetric Enamine Catalysis. Chem. Rev. 2007, 107, 12, 5471.
• Paek, S. et al. Recent Advances in Substrate-Controlled Asymmetric Induction Derived from Chiral Pool α-Amino Acids for Natural Product Synthesis. Molecules. 2016, 21, 7, 951.
• Palomo, C.; Oiarbide, M.; García, J. M. The Aldol Addition Reaction: An Old Transformation at Constant Rebirth. Chem. Eur. J. 2002, 8, 36.
• Santos et al. Atropoisomerismo: o efeito da quiralidade axial em substâncias bioativas. Química Nova. 2007, 30, 1, 125.
• Zou, Y.; Hörmann, F.M.; Bach, T. Iminium and enamine catalysis in enantioselective photochemical reactions. Chem. Soc. Rev., 2018, 47, 278-290. |
