Notícias
Publicação do livro “Química orgânica experimental: uma abordagem de química verde” de autoria de professores da UFSCar

Centro de Excelência para a Descoberta de Novos Alvos Moleculares: um modelo de interação público x privada

Comparison of the regiospecific distribution from triacylglycerols after chemical and enzymatic interesterification of high oleic sunflower oil and fully hydrogenated high oleic sunflower oil blend by carbon-13 nuclear magnetic resonance
Lopes, T.I.B.; Ribeiro, M.D.M.M. ; Ming, C.C.; Grimaldi, R.; Goncalves, L.A.G.; Marsaioli, A.J. Food Chem. 2016, 212, 641-647. DOI:10.1016/j.foodchem.2016.06.024

Multicomponent Synthesis of Cyclic Depsipeptide Mimics by Ugi Reaction Including Cyclic Hemiacetals Derived from Asymmetric Organocatalysis
de la Torre,A. F.; Rivera, D. G.; Concepción, O.; Echemendia, R.; Correa, A. G. ; Paixão, M. W. J. Org. Chem., 2016, 81, 803–809. DOI: 10.1021/acs.joc.5b02158

Continuous synthesis of hydantoins: intensifying the Bucherer–Bergs reaction
Monteiro, J.L.; Pieber, B.; Corrêa, A.G.; Kappe, C.O. Synlett 2016, 27, 83-87. DOI: 10.1055/s-0035-1560317
![Sonochemistry in organocatalytic enamine-azide [3 2] cycloadditions: A rapid alternative for the synthesis of 1,2,3-triazoyl carboxamides Sonochemistry in organocatalytic enamine-azide [3 2] cycloadditions: A rapid alternative for the synthesis of 1,2,3-triazoyl carboxamides](https://www.cersuschem.ufscar.br/news/sonochemistry-in-organocatalytic-enamine-azide-3-2-cycloadditions-a-rapid-alternative-for-the-synthesis-of-1-2-3-triazoyl-carboxamides/@@images/a984adea-048c-4d5a-af5f-7ddac7587dc4.png)
Sonochemistry in organocatalytic enamine-azide [3 2] cycloadditions: A rapid alternative for the synthesis of 1,2,3-triazoyl carboxamides
Xavier, D. M.; Goldani, B. S.; Seus, N.; Jacob, R. G.; Barcellos, T.; Paixao, M. W.; Luque, R.; Alves, D. Ultrasonics Sonochem. 2017, 34, 107-114. http://dx.doi.org/10.1016/j.ultsonch.2016.05.007

Magnetic ZSM-5 zeolite: a selective catalyst for the valorization of furfuryl alcohol to γ-valerolactone, alkyl levulinates or levulinic acid
Lima,T. M.; Lima, C. G. S.; Rathi, A. K.; Gawande, M. B.;Tucek, J.; Urquieta-González, E. A.; Zbořil, R.; Paixão, M. W.; Varma, R. S. Green Chem., 2016, 18, 5586-5593. DOI: 10.1039/C6GC01296E

Angiotensin converting enzyme immobilized on magnetic beads as a tool for ligand fishing
de Almeida, F. G.; Vanzolini, K. L.; Cass, Q. B. J. Pharmac. Biomed. Anal. 2017, 132, 159–164. DOI: 10.1016/j.jpba.2016.10.006