{"id":10,"date":"2016-06-27T16:48:36","date_gmt":"2016-06-27T16:48:36","guid":{"rendered":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/?page_id=10"},"modified":"2024-08-21T20:51:53","modified_gmt":"2024-08-21T20:51:53","slug":"publicacoes","status":"publish","type":"page","link":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/publicacoes\/","title":{"rendered":"Publica\u00e7\u00f5es"},"content":{"rendered":"
38) Souza, J. P. A.; Jacobs, A. K.; Piovan, L.<\/strong>; Campos, R. B. Org. Biomol. Chem. 2024, 22, 3926-3932. (DOI 10.1039\/D4OB00160E<\/a>)\n

Exploring the mechanism of the reductive amination of acetophenones\u00a0via<\/em> the Borch approach: the role of the acid catalyst<\/a><\/p>\n\n37) Aggio, B. B.; de Oliveira, A. R. M.; Piovan, L.<\/strong>*; Thomas, J. C.\u00a0Rev. Virtual Quim.<\/em>\u00a02023<\/strong>,\u00a015, 367-373<\/i>. (DOI\u00a010.21577\/1984-6835.20230006<\/a>)\n

A Chemoenzymatic Synthesis of Optically Active Mandelic Acid Employing Continuous-Flow Resolution of Cyanohydrin as a Key Step<\/a><\/p>\n\n36) Burich, M. D.; Bandeira, P. T.; de Oliveira, A. R. M.; Piovan, L.<\/strong>; Thomas, J. C. Rev. Virtual Quim.<\/em> 2023<\/strong>, 15, 213-220<\/i>. (DOI\u00a010.21577\/1984-6835.20220117<\/a>)\n

Non-linear Tendency Between Acyl Chain Length and Selectivity in Enzymatic Deacylation of Carboxylic Esters in Batch and Continuous-Flow<\/span><\/a><\/p>\n\n35) Zugman, T.; Durigon, M. C. S.; Campos, S. K.; da Silva, R. R.; da Silva, T. S.; de Oliveira, A. R. M.; Piovan, L.<\/strong>* ChemistrySelect 2022<\/strong>, 7, e2022038.\u00a0 \u00a0(DOI 10.1002\/slct.202203883<\/a>).\n

Exquisite use of Selenoesters as Recyclable Acyl Donors for Lipases-catalyzes kinetic resolution<\/a><\/p>\n\n34) Gomes, J. S. O.; da Silva, M. E.; Reis, J. S.; Piovan, L.*<\/strong>; Thomas, J. C. 2023<\/strong>, 4, 100603.<\/em>\u00a0(DOI 10.1016\/j.rechem.2022.100603)<\/a>\n

Brazilian contributions to Alcohol dehydrogenases-catalyzed reactions throughout the 21st century<\/a><\/p>\n\n33) Burich, M. D.; Bandeira. P. T.; de Oliveira, A. R. M.; Piovan, L.<\/strong>*; Thomas, J. C. Rev. Virtual Quim.<\/em> 2023<\/strong>, aceito<\/em>. (DOI\u00a010.21577\/1984-6835.2022011)<\/a>\n

Non-linear Tendency Between Acyl Chain Length and Selectivity in Enzymatic Deacylation of Carboxylic Esters in Batch and Continuous-Flow<\/a><\/p>\n\n32) Souza, J. P. A.; Bandeira, P. T.; Menezes, L. R. A.; Bespalhok, M. B.; Scariot, D. B.; Garcia, F. P.; Giese, S. O. K.; Hughes, D. L.; Nakamura, C. V; Barison, A.; Oliveira, A. R. M.; Campos, R. B.; Piovan, L.<\/strong>*\u00a0Chem. Eur. J. 2021, <\/em>14427-14437. <\/em>(DOI10.1002\/chem.202102287<\/a>).<\/em>\n

Synthesis, Mechanism Elucidation and Biological Insights of\u00a0 Tellurium(IV)-containing Heterocycles<\/a><\/p>\n\n31) Bom, M. A. T.; Botton, V.; Altheia, F. M.; Thomas. J. C.; Piovan, L.<\/strong>; C\u00f3rdova, J.; Mitchell, D. A.; Krieger, N.\u00a0 Biochem.<\/em> Eng. J<\/em>. 2021<\/strong>, 165<\/em>, 107817. (DOI 10.1016\/j.bej.2020.107817<\/a>)\n

Fermented solids that contain lipases produced by\u00a0Rhizopus microsporus<\/em>\u00a0have an\u00a0S<\/em>-enantiopreference in the resolution of secondary alcohols<\/a><\/span><\/p>\n

30) Borges, F. G.; Zugman, T.; Bandeira, P. T.; Dalmolin, M. C.; Scariot, D. B.; Garcia, F. P.; de Oliveira, A. R. M.; Nakamura, C. V.;\u00a0Piovan, L.<\/strong>*\u00a0J. Braz. Chem. Soc<\/em>.\u00a02021<\/strong>, 32, 462-475. (DOI\u00a010.21577\/0103-5053.20200201<\/a>)<\/p>\n

Complementary Performance of Organoselenides and Organotellurides as Antimicrobials Agents<\/a><\/p>\n\n29) Bandeira, P. T.; Gotor-Fern\u00e1ndez, V.; Piovan, L.*<\/strong>\u00a0Eur. J. Org. Chem<\/em>. 2020<\/strong>, 1129-1135. (DOI 10.1002\/ejoc.201901841<\/a>)\n

Stereoselective Bioreduction of Telluro-acetophenones to Optically Active Hydroxy Tellurides\u00a0<\/a><\/p>\n\n28) Dias, G. S.; Bandeira, P. T.; Jaerger, S.; Piovan, L<\/strong>.; Mitchell, D. A.; Wypych, F.; Krieger, N. Enzyme Microb. Tech.<\/em> 2019<\/strong>, 130<\/em>, 109365.\n

Immobilization of Pseudomonas cepacia<\/em> lipase on layered double hydroxide of Zn\/Al-Cl for kinetic resolution of rac-1-phenylethanol<\/a><\/p>\n\n27) Barros, H. R.; Santos, M. C.; Barbisa, L. R. S.; Piovan, L.<\/strong>; Riegel-Vidotti, I. C. J. Braz. Chem. Soc<\/em>. 2019<\/strong>, 00, 1-12. (DOI 10.21577\/0103-5053.20190127<\/a>)\n

Physicochemical Study of the Interaction between Gold Nanoparticles and Lipase from Candida sp. (CALB): Insights into the Nano-Bio Interface<\/a><\/p>\n\n26) Thomas, J. C.; Alnoch, R. C.; Costa, A. C. S.; Bandeira, P. T.; Burich, M. D.; Campos, S. K.;\u00a0 de Oliveira, A. R. M.; de Souza, E. M.; Pedrosa, F. O.; Krieger, N.; Piovan, L.*<\/strong> Molecular Catalysis<\/em> 2019<\/strong>, 473, 110402. (DOI 10.1016\/j.mcat.2019.110402<\/a>)\n

LipG9-mediated enzymatic kinetic resolution of racemates: expanding the substrate-scope for a metagenomic lipase<\/a><\/p>\n\n25) Bandeira, P. T.; Souza, J. P. A.; Scariot, D. B.; Garcia, F. P.; Nakamura, C. V.; de Oliveira, A. R. M.; Piovan, L.*<\/strong> ACS Med. Chem<\/em>. Lett<\/em>. 2019<\/strong>, 10<\/em>, 806-810. (<\/em>DOI 10.1021\/acsmedchemlett.9b00060<\/a>)\n

Diacetal Ditellurides as Highly Active and Selective Antiparasitic Agents Toward Leishmania amazonensis<\/em><\/a> <\/i><\/p>\n\n24) Bandeira, P. T.; Dalmolin, M. C.; de Oliveira, M. M.; Nunes, K. C.; Garcia, F. P.; Nakamura, C. V.; de Oliveira, A. R. M.; Piovan, L.*<\/strong> Bioorg. Med. Chem<\/em>. 2019<\/strong>, 27<\/em>, 410-415. (DOI 10.1016\/j.bmc.2018.12.017<\/a>)\n

Synthesis, Antioxidant Activity and Cytotoxicity of N<\/em>-Functionalized Organotellurides<\/a><\/p>\n\n23) Serres, J. D. S.; Bandeira, P. T.; Zappani, P. C.; Piovan, L.<\/strong>; Corazza, M. L.\u00a0J. Supercrit. Fluids<\/em> 2019<\/strong>, 143<\/em>, 330\u2013335. (DOI 10.1016\/j.supflu.2018.09.011<\/a>)\n

A greener bioreduction using baker\u2019s yeast cells in\u00a0supercritical carbon dioxide and glycerol system.<\/a><\/p>\n\n22) Dalmolin, M. C.; Bandeira, P. T.; Ferri, M.; de Oliveira, A. R. M.; Piovan, L<\/strong>.*<\/strong>\u00a0 J.\u00a0Organomet. Chem.<\/em>\u00a02018<\/strong>, 874, 32-39. (DOI 10.1016\/j.jorganchem.2018.08.007<\/a>)\n

Straighforward microwave-assisted synthesis of organochalcogen amines by reductive amination.<\/a><\/p>\n\n21) Teixeira, M. L.; Menezes, L. R. A.; Barison, A.; de Oliveira, A. R. M.; Piovan, L<\/strong>.*<\/strong> J. Org. Chem<\/em>. 2018<\/strong>, 83<\/em>, 7341-7346. (DOI 10.1021\/acs.joc.7b02971<\/a>)\n

Investigation of Chemical Stability of Dihalogenated\u00a0Organotelluranes in Organic\u2212Aqueous Media: The Protagonism of Water<\/a><\/p>\n\n20) Botton, V.; Piovan, L<\/strong>.; Meier, H. F.; Mitchell, D. A.; Cordova, J.; Krieger, N. Bioprocess Biosystems Eng<\/em>. 2018<\/strong>, 41<\/em>, 573-583. (DOI 10.1007\/s00449-018-1892-5<\/a>)\n

Optimization of biodiesel synthesis by esterification using a fermented solid produced by Rhizopus microsporus on sugarcane bagasse.<\/a><\/p>\n\n19) Bandeira, P. T.; Thomas, J.C.;\u00a0Oliveira, A. R. M.; Piovan, L<\/strong>.*<\/strong> J. Chem. Ed<\/em>. 2017<\/strong>, 94,\u00a0<\/em>800-805. (DOI 10.1021\/acs.jchemed.6b00606<\/a>)\n

Lipase-Mediated Kinetic Resolution: An Introductory Approach to\u00a0Practical Biocatalysis.<\/a><\/p>\n\n18) Thomas, J. C.; Burich, M. D.; Bandeira, P. T.; \u00a0Oliveira, A. R. M.;\u00a0Piovan, L<\/strong>.*<\/strong> Biocatalysis<\/em>\u00a02017<\/strong>, 3<\/em>, 27- 36. (DOI 10.1515\/boca-2017-0003<\/a>)\n

Biocatalysis in continuous-flow mode: A case study in the enzymatic kinetic resolution of secondary alcohols via acylation and deacylation reactions mediated by Novozym 435.<\/a><\/p>\n\n17)\u00a0da Silva, T. S.; Campos, S. K.;\u00a0Oliveira, A. R. M.; Piovan, L<\/strong>.*<\/strong> J. Mol. Catal. B, Enzymatic\u00a0<\/em>2016<\/strong>, 133<\/em>, S317\u2013S323. (10.1016\/j.molcatb.2017.02.001<\/a>)\n

An unexpected inversion of CAL-B enantiopreference based on substrate engineering of 2-bromoesters: Effect of (R<\/em>)-1-phenylethyl moiety.<\/a><\/p>\n\n16)\u00a0Thomas, J. C.; Aggio, B. B.;\u00a0Oliveira, A. R. M.; Piovan, L<\/strong>.*<\/strong> Eur. J. Org. Chem.<\/em> 2016<\/strong>, 5964\u20135970. (DOI 10.1002\/ejoc.201601028<\/a>)\n

High-Throughput Preparation of Optically Active Cyanohydrins\u00a0Mediated by Lipases.<\/a><\/p>\n\n15) Barros, H. R.; Piovan, L.<\/strong>; Sassaki, G. L.; Sabry, D. A.; Mattoso, N.; Nunes, A. M.; Meneghetti, M. R. Riegel-Vidotti, I. C.\u00a0Carbohydrate Polymers 2016<\/strong>,\u00a0<\/em>152, 479\u2013486. (DOI 10.1016\/j.carbpol.2016.07.018<\/a>)\n

Surface interactions of gold nanorods and polysaccharides: From clusters to individual nanoparticles<\/a><\/p>\n\n14) Bandeira, P. T.; Alnoch, R. C.; Oliveira, A. R. M.; Souza, E. M.; Pedrosa, F. O.; Piovan, L.<\/strong>*\u00a0 J. Mol. Catal. B, Enzymatic<\/em> 2016<\/strong>, 125, 58-63. (j.molcatb.2015.12.010<\/a>)\n

Enzymatic kinetic resolution of aliphatic sec-alcohols by LipG9, a metagenomic lipase.<\/a><\/p>\n\n13) de Oliveira, A. R. M.; Piovan, L.<\/strong>; Simonelli, F.; Barison, A.; Santos, M. F. C. de Mello, M. B. M.\u00a0\u00a0J. Organomet. Chem.\u00a0<\/em>2016<\/strong>, 806<\/em>, 54-59. (DOI 10.1016\/j.jorganchem.2016.01.028<\/a>)\n

A 77<\/sup>Se NMR study of elemental selenium reduction using NaBH4<\/sub>.<\/a><\/p>\n\n12) Alnoch, R. C.; Martini, V. P. ; Costa, A. C. S.; Piovan, L.<\/strong>; Muller-Sanstos, M.; Souza, E. M.; Pedrosa, F. O.; Mitchell, D.; Krieger, N. PLoS One<\/em>, 2015<\/strong>, 10. (DOI 10.1371\/journal.pone.0114945<\/a>)\n

Immobilization and Characterization of a New Regioselective and Enantioselective Lipase Obtained from a Metagenomic Library.<\/a><\/p>\n\n11) de Mello, M. B.M.; Clososki, G. C.; Piovan, L.<\/strong>; de Oliveira, A. R.M. \u00a0J.\u00a0Organomet. Chem.<\/em>\u00a02015<\/strong>, 794<\/em>, 11-16. (DOI 10.1016\/j.jorganchem.2015.06.022<\/a>)\n

An alternative approach to differentially substituted 2-oxazoline chalcogen derivatives.<\/a><\/p>\n\n10) Piovan, L.<\/strong>; Milani, P.; Silva, M. S.; Moraes, P. G.; Demasi, M.; Andrade, L. H. \u00a0Eur. \u00a0J. Med. Chem.<\/em>\u00a02014<\/strong>, 73<\/em>, 280-285. (DOI 10.1016\/j.ejmech.2013.12.011<\/a>)\n

20S proteasome as novel biological target for organochalcogenanes.<\/a><\/p>\n\n9) Madalozzo, A. D.; Muniz, L. S.; Baron, A. M.; Piovan, L.<\/strong>; Mitchell, D. A.; Krieger, N. Biocatalysis and Agricultural Biotechnology<\/em> 2014<\/strong>, 3<\/em>, 13-19. (DOI 10.1016\/j.bcab.2013.12.005<\/a>)\n

Characterization of an immobilized recombinant lipase from Rhizopus oryzae<\/em>: Synthesis of ethyl-oleate.<\/a><\/p>\n\n8) Piovan, L.<\/strong>; Wu, L.; Zhang, Z.; Andrade, L. H. \u00a0Org. Biomol. Chem.\u00a0<\/em>2011<\/strong>, 9<\/em>, 1347-1351. (DOI 10.1039\/C0OB01050B<\/a>)\n

Hypervalent Organochalcogenanes as Inhibitors of Protein Tyrosine Phosphatases.<\/a><\/p>\n\n7) Piovan, L.<\/strong>; Alves, M. F. M.; Juliano, L.; Bromme, D.; Cunha, R. L. O. R.; Andrade, L. H. Bioorg.\u00a0Med. Chem.<\/em>\u00a02011<\/strong>, 19<\/em>, 2009-2014. (DOI 10.1016\/j.bmc.2011.01.054<\/a>)\n

Structure-Activity Relationships of Hypervalent Organochalcogenanes as inhibitors of cysteine cathepsins V and S.<\/a><\/p>\n\n6) Piovan, L<\/strong>.; Pasquini, M. D.; Andrade, L. H. Molecules<\/em> 2011<\/strong>, 16, 8098-8109. (DOI 10.3390\/molecules16098098<\/a>)\n

Enzymatic Kinetic Resolution of tert-Butyl 2-(1-Hydroxyethyl)phenylcarbamate, A Key Intermediate to Chiral Organoselenanes and Organotelluranes.<\/a><\/p>\n\n5) Piovan, L.<\/strong>; Kagohara, E.; Vale, J. A.; Comasseto, J. V.; Shoenlein-Crusius; Andrade, L. H.; Porto, A. L. M. Food Technol.\u00a0 Biotechnol.\u00a0<\/em>2011<\/strong>, 49<\/em>, 460-464.\n

Demethylation of N,N-Dimethylbenzenamine and N,N,3-Trimethylbenzenamine by Whole Cells of Aspergillus terreus.<\/em><\/a><\/p>\n\n4) Piovan, L.<\/strong>; Alves, M. F. M.; Juliano, L.; Bomme, D.; Cunha, R. L. O. R ; Andrade, L. H. J. Braz. Chem. Soc.\u00a0<\/em>2010<\/strong>, 21, 2108-2118. (DOI 10.1590\/S0103-50532010001100012<\/a>)\n

Chemoenzymatic synthesis of organoselenium(IV) compounds and their evaluation as cysteine protease inhibitors.<\/a><\/p>\n\n3) Andrade, L. H.; Piovan, L.<\/strong>; Pasquini, M. D. Tetrahedron: Asymm.<\/em>\u00a02009<\/strong>, 20<\/em>, 1521-1525. (DOI 10.1016\/j.tetasy.2009.05.033<\/a>)\n

Improving the enantioselective bioreduction of aromatic ketones mediated by Aspergillus terreus<\/em> and Rhizopus oryzae<\/em>: the role of glycerol as a co-solvent.<\/a><\/p>\n\n2) Piovan, L.<\/strong>; Kagohara, E.; Ricci, L. C.; Keppler, A. F.; Andrade, L. H.; Comasseto, J. V.; Porto, A. L. M.\u00a0Tetrahedron. <\/em>Asymm.\u00a0<\/em>2008<\/strong>, 19, 2385-2389. (DOI 10.1016\/j.tetasy.2008.10.003<\/a>)\n

Chemoselective screening for the reduction of a chiral functionalised (\u00b1)-2<\/a>-(<\/a>phenylthio)cyclohexanone by whole cells of Brazilian micro-organisms.<\/a><\/p>\n\n1) Piovan, L.<\/strong>; Capelari, M.; Andrade, L. H.; Comasseto, J. V.; Porto, A. L. Tetrahedron: Asymm.<\/em>\u00a02007<\/strong>, 18<\/em>, 1398-1402. (DOI 10.1016\/j.tetasy.2007.05.036<\/a>)\n

Biocatalytic reduction of a racemic selenocyclohexanone by Brazilian basidiomycetes<\/em>. <\/a><\/p><\/div><\/div><\/div><\/div><\/div><\/div>","protected":false},"excerpt":{"rendered":"

38) Souza, J. P. A.; Jacobs, A. K.; Piovan, L.; Campos, R. B. Org. Biomol. Chem. 2024, 22, 3926-3932. (DOI 10.1039\/D4OB00160E) Exploring the mechanism of the reductive amination of acetophenones\u00a0via the Borch approach: the role of the acid catalyst 37) Aggio, B. B.; de Oliveira, A. R. M.; Piovan, L.*; Thomas, J. C.\u00a0Rev. Virtual Quim.\u00a02023,\u00a015, […]<\/p>\n","protected":false},"author":7,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-10","page","type-page","status-publish","hentry","post"],"_links":{"self":[{"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/pages\/10","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/users\/7"}],"replies":[{"embeddable":true,"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/comments?post=10"}],"version-history":[{"count":108,"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/pages\/10\/revisions"}],"predecessor-version":[{"id":633,"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/pages\/10\/revisions\/633"}],"wp:attachment":[{"href":"http:\/\/www.quimica.ufpr.br\/paginas\/leandro-piovan\/wp-json\/wp\/v2\/media?parent=10"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}