{"id":14,"date":"2015-07-28T13:13:48","date_gmt":"2015-07-28T16:13:48","guid":{"rendered":"https:\/\/www.sbq.org.br\/divisao_organica\/premio-nicola-petragnani\/"},"modified":"2024-01-18T16:09:39","modified_gmt":"2024-01-18T19:09:39","slug":"premio-nicola-petragnani","status":"publish","type":"page","link":"https:\/\/www.sbq.org.br\/organica\/premio-nicola-petragnani\/","title":{"rendered":"Pr\u00eamio Nicola Petragnani"},"content":{"rendered":"<p><span style=\"line-height: 1.538em;\">Desde 2007 na 30<sup>a<\/sup> RASBQ, al\u00e9m dos tradicionais pr\u00eamios oferecidos pela SBQ aos melhores p\u00f4steres, a Divis\u00e3o de Qu\u00edmica Org\u00e2nica passou a oferecer o Pr\u00eamio Nicola Petragnani, para o melhor trabalho de aluno de p\u00f3s-gradua\u00e7\u00e3o, que fizesse parte da SBQ e estivesse submetido a Divis\u00e3o de Qu\u00edmica Org\u00e2nica. O pr\u00eamio oferecido pela DQO, recebeu o nome de um pesquisador de grande import\u00e2ncia para a Qu\u00edmica Org\u00e2nica brasileira e que sempre merece ser relembrado.<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">Abaixo segue a lista de trabalhos premiados desde a cria\u00e7\u00e3o do Pr\u00eamio Nicola Petragnani.<\/span><\/p>\n<p><strong>44<sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RAVSBQ (2021)<\/strong>:<\/span><\/p>\n<p>N\u00e3o houve premia\u00e7\u00e3o na reuni\u00e3o anual no formato virtual em 2021.<\/p>\n<p><strong>43<sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RAVSBQ (2020)<\/strong>:<\/span><\/p>\n<p>N\u00e3o houve premia\u00e7\u00e3o na reuni\u00e3o anual no formato virtual em 2020.<\/p>\n<p><strong>42<sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2019)<\/strong>:<\/span><\/p>\n<p>&#8211;&gt; Vin\u00edcius R. do Nascimento (PG) e Leandro H. Andrade &#8211; IQ-USP<\/p>\n<p>&#8211; Explorando a reatividade do radical carbamo\u00edla para cria\u00e7\u00e3o da primeira rota sint\u00e9tica das coixespirolactamas A e B<\/p>\n<p><strong><span style=\"font-size: 13.008px;\">41<\/span><sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2018)<\/strong>:<\/span><\/p>\n<p>&#8211;&gt; Alexander G. Talero (PG), Bruna S. Martins (PQ) e Ant\u00f4nio C. B. Burtoloso (PQ) &#8211; IQSC-USP<\/p>\n<p>&#8211; Arylation of \u03b2-ketosulfoxonium ylides with arynes: a direct synthesis of pro-chiral ylides and mono-arylated ketones<\/p>\n<p><strong style=\"font-size: 13.008px;\"><span style=\"line-height: 1.538em;\">40<\/span><sup>a<\/sup><\/strong><span style=\"font-size: 13.008px; line-height: 1.538em;\"><strong>RASBQ (2017)<\/strong>: <\/span><\/p>\n<p><span style=\"font-size: 13.008px; line-height: 1.538em;\">N\u00e3o houve premia\u00e7\u00e3o na reuni\u00e3o conjunta com a IUPAC World Congress (S\u00e3o Paulo, SP)<\/span><\/p>\n<p style=\"font-size: 13.008px;\"><strong style=\"font-size: 13.008px;\"><span style=\"line-height: 1.538em;\">39<\/span><sup>a<\/sup><\/strong><span style=\"font-size: 13.008px; line-height: 1.538em;\"><strong>RASBQ (2016)<\/strong>:<\/span><\/p>\n<p style=\"font-size: 13.008px;\"><span style=\"font-size: 13.008px;\">&#8211;&gt;&nbsp;<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">Luma Fritsch&nbsp;<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">(PG), Eric S. Sales (PG) e Aloir A. Merlo<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">&nbsp;(PQ) &#8211; UFRGS<\/span><\/p>\n<p style=\"font-size: 13.008px;\">&#8211; S<strong style=\"font-size: 13.008px;\"><span style=\"font-size: 10pt; line-height: 14.2667px; font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; color: rgb(51, 51, 51); background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-weight: normal;\">ynthesis and photophysical properties of perylene bisimides from isoxazolines and isoxazoles<\/span><\/strong><\/p>\n<p style=\"font-size: 13.008px;\"><span style=\"font-size: 13.008px;\">&#8211;&gt;&nbsp;<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">Ajmir Khan<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">&nbsp;(PG) e Luiz Fernando da Silva Jr<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">&nbsp;(PQ) &#8211; USP<\/span><\/p>\n<p style=\"font-size: 13.008px;\">&#8211; Ring expansions promoted by iodine (III): synthesis of heterocycles<\/p>\n<p><strong style=\"font-size: 13.008px;\"><span style=\"line-height: 1.538em;\">38<\/span><sup>a<\/sup><\/strong><span style=\"font-size: 13.008px; line-height: 1.538em;\"><strong>RASBQ (2015)<\/strong>:<\/span><\/p>\n<p><span style=\"font-size: 13.008px;\">&#8211;&gt;&nbsp;<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">Luiz F. T. Novaes<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">&nbsp;(PG) e Ronaldo A. Pilli<\/span><span style=\"color: rgb(51, 51, 51); font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; font-size: 10pt;\">&nbsp;(PQ) &#8211; UNICAMP<\/span><\/p>\n<p>&#8211;&nbsp;<strong style=\"font-size: 13.008px;\"><span style=\"font-size: 10pt; line-height: 107%; font-family: &quot;Lucida Sans Unicode&quot;, sans-serif; color: rgb(51, 51, 51); background-image: initial; background-position: initial; background-size: initial; background-repeat: initial; background-attachment: initial; background-origin: initial; background-clip: initial; font-weight: normal;\">Total synthesis and structural elucidation of cryptolatifolione<\/span><\/strong><\/p>\n<p><strong><span style=\"line-height: 1.538em;\">37<\/span><sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2014):<\/strong><\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt;&nbsp;<\/span><span style=\"line-height: 1.538em;\">Rossini, A. F. C. (PG); Raminelli, C. (PQ) &#8211; UNIFESP<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211; Estudo visando \u00e0 s\u00edntese total c<\/span><span style=\"line-height: 1.538em;\">onvergente do alcaloide 7-oxoisotebaina<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt;&nbsp;<\/span><span style=\"line-height: 1.538em;\">Miranda, A. C. M. (PG); Silva Da, C. M. (PG); Geraldo, G. C. (PG); Barbosa, L. C. A. (PQ); Demuner, A. J. (PQ); Forlani, G. (PQ) &#8211; UFV<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&nbsp;<\/span><span style=\"line-height: 1.538em;\">S\u00edntese e avalia\u00e7\u00e3o fitot\u00f3xica de benzopironas an\u00e1logas ao alternariol<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt;&nbsp;<\/span><span style=\"line-height: 1.538em;\">Santos, F. M. (PG); Batista, J. H. C. (PG); Clososki, G. C. (PQ) &ndash; USP<\/span><\/p>\n<p>&#8211; Funcionaliza\u00e7\u00e3o de nitrilas heteroc\u00edclicas utilizando a base organomet\u00e1lica TMPMgCl.LiCl<\/p>\n<p><strong><span style=\"line-height: 1.538em;\">36<\/span><sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2013):<\/strong><\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt;&nbsp;<\/span><span style=\"line-height: 1.538em;\">Lucca Jr. de, E. C. (PG); Dias, L. C. (PQ) &#8211; IQ-UNICAMP.<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">-S\u00edntese do fragmento C23-C35 do marinisporol\u00eddeo A.<\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt; Franco, L. L. (PG); Alves, R. J. (PQ); Filho, J. D. S. (PQ) &#8211; UFMG.<\/span><\/p>\n<p>N-(2-acetamido-3,4,6-tri-O-acetil-2-desoxi-\u03b2-D-glicopiranosil)-1-naftalenossulfonamida: estudos de m\u00e9todos para sua obten\u00e7\u00e3o<\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt; Lordello, L. D. (PG); Bernardim, B. (PG); Burtoloso, A. C. B. (PQ) &#8211; IQSC-USP<\/span><\/p>\n<p>Diazocetonas \u03b1,\u03b2-insaturadas como precursoras de alcaloides piperidinicos e quinolizidinicos hidroxilados<\/p>\n<p>&#8211;&gt;&nbsp;<span style=\"line-height: 1.538em;\">Oliveira, C. C. (PG); Angnes, R. A. (PG); Correia, C. R. D. (PQ) &ndash; UNICAMP<\/span><\/p>\n<p>Arila\u00e7\u00e3o enantiosseletiva de olefinas ac\u00edclicas via reac\u00e3o de Heck-Matsuda. s\u00edntese e aplica\u00e7\u00f5es sint\u00e9ticas de 4-arillactonas<\/p>\n<p><strong><span style=\"line-height: 1.538em;\">35<\/span><sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2012):<\/strong><\/span><\/p>\n<p><span style=\"line-height: 1.538em;\">&#8211;&gt;&nbsp;<\/span><span style=\"line-height: 1.538em;\">Rossini, A. F. C. (IC); Frota, C. (PG); Raminelli, C. (PQ) &#8211; UFGD<\/span><\/p>\n<p>&#8211; Rea\u00e7\u00e3o de acoplamento seletiva entre 2,6-diiodoanis\u00f3is e alcinos terminais catalisada por Pd(PPh3)2Cl2 e CuI<\/p>\n<p>&#8211;&gt;&nbsp;<span style=\"line-height: 1.538em;\">Santos, E. A. F. (IC); Oliveira, C. C. (PG); Correia, C. R. D. (PQ) &#8211; UNICAMP<\/span><\/p>\n<p>&#8211; Arila\u00e7\u00e3o de olefinas c\u00edclicas n\u00e3o ativadas via rea\u00e7\u00e3o de Heck-Matsuda e sua aplica\u00e7\u00e3o de s\u00edntese de an\u00e1logos de C-aril-nucleos\u00eddeos<\/p>\n<p>&#8211;&gt;&nbsp;<span style=\"line-height: 1.538em;\">Oliveira, C. C. (PG); Salles Jr., A. G. (PQ); Correia, C. R. D. (PQ) &ndash; UNICAMP<\/span><\/p>\n<p>&#8211; Primeiros exemplos da rea\u00e7\u00e3o de Heck-Matsuda enantiosseletiva<\/p>\n<p><strong><span style=\"line-height: 1.538em;\">30<\/span><sup>a<\/sup><\/strong><span style=\"line-height: 1.538em;\"><strong>RASBQ (2007):<\/strong><\/span><\/p>\n<p><span style=\"line-height: 1.538em;\"><span style=\"font-size: 13.008px;\">&#8211;&gt;<\/span>&nbsp;<\/span><span style=\"line-height: 1.538em;\">Cristiano Raminelli (PG), Jo\u00e3o Gargalaka (IC), Cl\u00e1udio da Cruz Silveira (PQ), Jo\u00e3o V. Comasseto (PQ) &#8211; USP<\/span><\/p>\n<p><span style=\"font-size: 13.008px;\">-Acoplamento entre Teluretos Butilvin\u00edlicos e Reagentes Organomet\u00e1licos Catalisado por Complexos de N\u00edquel<\/span><\/p>\n<p>&nbsp;<\/p>\n<p><a href='http:\/\/www.sbq.org.br\/wp-content\/uploads\/sites\/13\/2023\/12\/captura_de_tela_2015-07-28_as_15.13.15.png'>http:\/\/www.sbq.org.br\/wp-content\/uploads\/sites\/13\/2023\/12\/captura_de_tela_2015-07-28_as_15.13.15.png<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Desde 2007 na 30a RASBQ, al\u00e9m dos tradicionais pr\u00eamios oferecidos pela SBQ aos melhores p\u00f4steres, a Divis\u00e3o de Qu\u00edmica Org\u00e2nica passou a oferecer o Pr\u00eamio Nicola Petragnani, para o melhor trabalho de aluno de p\u00f3s-gradua\u00e7\u00e3o, que fizesse parte da SBQ e estivesse submetido a Divis\u00e3o de Qu\u00edmica Org\u00e2nica. O pr\u00eamio oferecido pela DQO, recebeu o [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"institucional","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/pages\/14"}],"collection":[{"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/comments?post=14"}],"version-history":[{"count":1,"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/pages\/14\/revisions"}],"predecessor-version":[{"id":56,"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/pages\/14\/revisions\/56"}],"wp:attachment":[{"href":"https:\/\/www.sbq.org.br\/organica\/wp-json\/wp\/v2\/media?parent=14"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}