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PUBLICATIONS

 
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42) Stivanin, M. L.; Gallo, R. D. C.; Spadeto, J. P. M.; Cormanich, R. A.; Jurberg, I. D.*; A Visible Light-Mediated Three-Component Strategy Based on the Ring-Opening of Cyclic Ethers with Aryldiazoacetates and Nucleophiles. Org. Chem. Frontiers, 2022, accepted.

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41) Munaretto, L. S.[+]; dos Santos, C. Y.[+]; Gallo, R. D. C.; Okada Jr., C. Y.; Deflon, V. M.; Jurberg, I. D.*; Visible-Light-Mediated Strategies to Assemble Alkyl 2-Carboxylate-2,3,3-Trisubstituted -Lactams and 5-Alkoxy-2,2,4-Trisubstituted Furan-3(2H)-ones Using Aryldiazoacetates and Aryldiazoketones. Org. Lett. 2021, 23, 9292–9296. ([+] Equal contributions)

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40) Stivanin, M. L.; Duarte, M.; Leão, L. P. M. O.; Saito, F. A.; Jurberg, I. D.*; Visible Light-Mediated Strategies for the Preparation of Oxime Ethers Derived from O-H Insertions of Oximes into Aryldiazoacetates. J. Org. Chem. 2021, 86, 17528–17532.

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39) Gallo, R. D. C.; Duarte, M.; da Silva, A. F.; Okada Jr., C. Y.; Deflon, V. M.; Jurberg, I. D.*; A Selective C-C Bond Cleavage Strategy Promoted by Visible Light. Org. Lett. 2021, 23, 8916–8920.

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38) Jurberg, I. D.;* Criação do Grupo Jurberg e Desenvolvimento de suas Pesquisas em Catálise Homogênea, Química de Heterociclos e Fotoquímica com Luz Visível, Síntese Orgânica no Brasil, SBQ, 2021, accepted (Book Chapter)

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37) Berlinck, R. G. S.*; Bernardi, D. I.; Fill, T. P.; Fernandes, A. A. G.; Jurberg, I. D.; The Chemistry and Biology of Guanidine Secondary Metabolites. Nat. Prod. Rep., 2021, 38, 586-667.

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36) Yang, Z.[+]; Stivanin, M. L.[+]; Jurberg, I. D.*; Koenigs, R. M.*; Visible Light-Promoted Reactions with Diazo Compounds: A Mild and Practical Strategy towards Free Carbene Intermediates. Chem. Soc. Rev., 2020, 49, 6833-6847. ([+] Equal contributions)

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35) da Silva, A. F.; Leonarczyk, I. A.; Ferreira, M. A. B.*; Jurberg, I. D.*; Diastereodivergent Aminocatalyzed Spirocyclization Strategies using 4-Alkylideneisoxazol-5-ones and Methyl Vinyl Ketones. Org. Chem. Frontiers, 2020, 7, 3599-3607.

- Selected as internal cover

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34) Okada Jr., C. Y.; dos Santos, C. Y.; Jurberg, I. D.*; Blue light-promoted N-H insertion of amides, isatins, sulfonamides and imides into aryldiazoacetates: synthesis of unnatural alpha-aryl amino acid derivatives. Tetrahedron 2020, 76, 131316 (invited submission, in honor of Prof. Nuno Maulide, recipient of the 2020 Tetrahedron Young Investigator Award)

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33) Sigrist, R.; Luhavaya, H.; McKinnie, S. M. K.; da Silva, A. F.; Jurberg, I. D.; Moore, B. S.*; de Oliveira, L. G.*; Nonlinear Biosynthetic Assembly of Alpiniamide by a Hybrid cis/trans-AT PKS-NRPS, ACS Chem. Biol. 2020, 15, 1067-1077.

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32) Fernandes, A. A. G.; Jurberg, I. D.*; Synergisms Between Metal and Photoredox Catalysis: Deconvoluting Complex Systems, Química Nova 2020, 43, 928-950.

Graphical Abstract_Aryldiazoacetates and

31) da Silva, A. F.; Afonso, M. A. S.; Cormanich, R. A.; Jurberg, I. D.* Room Temperature Coupling of Aryldiazoacetates with Boronic Acids Enhanced by Blue Light Irradiation. Chem. Eur. J. 2020, 26, 5648-5653.

- Selected as Internal Cover

- Highlighted in the Wiley Virtual Issue "Hot Topic: C-C Coupling"

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30) Stivanin, M. L.; Fernandes, A. A. G.; da Silva, A. F.; Okada Jr, C. Y.; Jurberg, I. D.* Blue Light-Promoted N-H Insertion of Carbazoles, Pyrazoles and 1,2,3-Triazoles into Aryldiazoacetates. Adv. Synth. Catal. 2020, 362, 1106-1111.

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29) Quevedo-Acosta, Y.; Jurberg, I. D.*; Gamba-Sánchez, D.* Activating Imides with Triflic Acid: A General Intramolecular Aldol Condensation Strategy Towards Indolizidine, Quinolizidine and Valmerin Alkaloids. Org. Lett. 2020, 22, 239-243.

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28) Thurow, S.[+]; Fernandes, A. A. G.[+]; Quevedo-Acosta, Y.; Oliveira, M. F.; Oliveira, M. G.; Jurberg, I. D.* Preparation of Organic Nitrates from Aryldiazoacetates and Fe(NO3)3.9H2O. Org. Lett. 2019, 21, 6909-6913 ([+]: equal contributions)

- Highlighted in the Organic Chemistry Portal

- Selected for the Virtual Issue Celebrating Chemistry in Latin America of Org. Lett./ J. Org. Chem./ Organometallics

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27) Fernandes, A. A. G.[+]; da Silva, A. F. [+]; Okada Jr., C. Y. [+]; Suzukawa, V.; Cormanich, R. A.; Jurberg, I. D.* General Platform for the Conversion of Isoxazol-5-ones to 3,5-Disubstituted Isoxazoles via Nucleophilic Substitutions and Palladium Catalyzed Cross-Coupling Strategies Eur. J. Org. Chem. 2019 3022-3034 ([+]: equal contributions)

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26) Fernandes, A. A. G.; Stivanin, M. L.; Jurberg, I. D.* RuCl3/PPh3 - Catalyzed Direct Conversion of Isoxazol-5-ones to 2,3-Disubstituted Pyridines.  ChemistrySelect 2019, 4, 3360-3365.

- Top 10% most downloaded paper of ChemistrySelect in the period Jan 2018-Dec 2019

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25) Fernandes, A. A. G.; da Silva, A. F.; Thurow, S.; Okada Jr., C. Y.; Jurberg, I. D.*  Isoxazol-5-ones: Unusual Heterocycles with Great Synthetic Potential. Targets in Heterocyclic Systems 2019, 409-435. Eds. Attanazi, O. A.; Merino, P.; Spinelli, D. Italian Society of Chemistry. (Book Chapter)

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24) Fill, T. P.*; Pallini, H. F.;  Din, Z. U.; Jurberg, I. D.;  Silva, J. V.; Rodrigues-Filho, E. Conjugation of Antifungal Benzoic Acid Derivatives as a Path for Detoxification in Penicillium brasilianum, an Endophite from Melia azedarach. Bioorg. Chem. 201881, 367.

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23) Bertuzzi, D.; Becher, T.; Capreti, N. M. R.; Almeida, J.; Jurberg, I. D.; Megiatto Jr., J. D.; Ornelas, C.* General Protocol to Obtain D-Glucosamine From Biomass Residues: Shrimp Shells, Cicada Sloughs and Cockroaches. Global Challenges 20182, 1800046

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22) Jurberg, I. D.*; Davies, H. M. L.* Blue Light-Promoted Photolysis of Aryldiazoacetates Chem. Sci. 20189, 5112-5118.

Abstract Synthesis2018_Review Isoxazolon

21) da Silva, A. F.; Fernandes, A. A. G.; Thurow, S.; Stivanin, M. L.; Jurberg, I. D.* Isoxazol-5-ones as Strategic Building Blocks in Organic Synthesis. Synthesis 201850, 2473–2489 (Invited Short Review)

Abstract Chem Sci2018_Claisen Mechanism.

20) Maryasin, B.*; Kaldre, D.; Galaverna, R.; Klose, I.; Ruider, S.; Drescher, M.; Kählig, H.; Gonzalez, L.; Eberlin, M.; Jurberg, I. D.*; Maulide, N.* Unusual Mechanisms in Claisen Rearrangements: an Ionic Fragmentation leading to a meta-Selective Rearrangement. Chem. Sci. 2018, 9, 4124-4131.

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19) Stivanin, M. L.; Duarte, M.; Sartori, C.; Capreti, N. M. R.; Angolini, C. F. F.; Jurberg, I. D.* An Aminocatalyzed Michael Addition/Iron-mediated Decarboxylative Cyclization Sequence for the Preparation of 2,3,4,6-Tetrasubstituted Pyridines: Scope and Mechanistic Insights. J. Org. Chem. 201782, 10319–10330.

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18) Jurberg, I. D.*; Davies, H. M. L.* Rhodium- and Non-Metal-Catalyzed Approaches for the Conversion of Isoxazol-5-ones to 2,3-Dihydro-6H-1,3-Oxazin-6-ones. Org Lett. 201719, 5158–5161.

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17) Jurberg, I. D.* An Aminocatalyzed Stereoselective Strategy for the Formal alpha-Propargylation of Ketones. Chem. Eur. J. 2017, 23, 9716-9720.

- Selected as "Hot Paper"

- Selected as Internal Cover

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16) Lima, C.; Lima, T.;  Duarte, M.; Jurberg, I. D.*; Paixão, M. W.*; Organic Synthesis Enabled by Light-Irradiation of EDA Complexes: Theoretical Background and Synthetic Applications. ACS Catalysis2016, 6, 1389-1407 (Review)

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15) Capreti, N. M. R.; Jurberg, I. D.*; Comprehensive Organic Chemistry Experiments for the Laboratory Classroom 2016, RSC Eds. Afonso, C. A. M.; Candeias, N. R.; Simão, D. P.; Trindade, A. F.;  Coelho, J. A. S; Tan, B.; Franzén, R. (Book chapters)

   i)  Preparation of Diethyl 2,3-O-isopropylidene-L-tartrate
   ii) Preparation of (4R,5R)-4,5-Bis(diphenylhydroxymethyl)-2,2-dimethyldioxolane ((-)-TADDOL)

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14) Capreti, N. M. R.; Jurberg, I. D.*; Michael Addition of Soft Carbon Nucleophiles to Alkylidene Isoxazol-5-ones: a Divergent Entry to beta-Branched Carbonyl Compounds.  Org. Lett. 2015, 17, 2490-2493.

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13) Jurberg, I. D.*; Synthèse d´Alcynes et Nouvelles Transformations Catalysées par l´Or(I), 2014, Presses Académiques Francophones. (Book, 500 pages).

Post-Doctoral and Graduate Studies

12) Silvi, M.; Arceo, E.; Jurberg, I. D.; Cassani, C.; Melchiorre, P.*; Enantioselective Organocatalytic Alkylation of Aldehydes and Enals Driven by the Direct Photoexcitation of Enamines J. Am. Chem. Soc. 2015, 137, 6120.

   - Highlighted in SYNFACTS 2015, 7, 765

11) Kandukuri, S.; Bahamonde, A.; Chatterjee, I.; Jurberg, I. D.; Escudero-Adán, E.; Melchiorre, P.*;   X-Ray Characterization of an EDA Complex which Drives the Photochemical Alkylation of Indoles. Angew. Chem. Int. Ed. 2015, 54, 1485.

10) Arceo, E.[+]; Jurberg, I. D.[+]; Álvarez-Fernández, A.; Melchiorre, P.*; Photochemical activity of a key donor-acceptor complex can drive stereoselective catalytic α-alkylation of aldehydes. Nature Chem. 2013, 750.([+]: equal contributions)

   - Highlighted in SYNFACTS 2013, 9, 11, 1229.

9) Jurberg, I. D.; Chatterjee, I.; Tannert, R.; Melchiorre, P.* When asymmetric aminocatalysis meets the vinylogy principle. Chem. Commun. 2013, 49, 4869. (Review)

8) Jurberg, I. D.; Ikeda, K.; Antwi-Omane, D.; Gagosz, F.* Synthesis of Functionalized Chromenes and Benzofurans from Aryloxy Propargyl Malonates. Isr. J. Chem. 2013, 53, 915.

7) Peng, B.; O’Donnovan, D.[+]; Jurberg, I.D.[+]; Maulide, N.*; Dual Nucleophilic/Electrophilic Capture of In-Situ Generated Iminium Ethers: Towards the Synthesis of Functionalized Amide Building Blocks. Chem. -Eur. J.  2012, 18, 16292. ([+]: equal contributions)

6) Jurberg, I. D.; Peng, B.; Woestefeld, E.; Wasserloos, M.; Maulide, N.*; Intramolecular Redox-Triggered C-H Functionalization. Angew. Chem. Int. Ed. 2012, 51, 1950.

   - Selected as "Hot Paper" 

5) Jurberg, I. D.*; Spotlight Article: Silver Carbonate. Synlett 20/ 2011, S375. (Highlight)

4) Jurberg, I. D.; Gagosz, F.*; Formation of Cinnoline Derivatives by a Gold(I)-Catalyzed Hydroarylation of N-Propargyl-N’-Arylhydrazines. J. Organomet. Chem. 2011, 696, 37.

3) Jurberg, I. D.; Odabachian, Y.; Gagosz, F.*; Hydroalkylation of Alkynyl Ethers via Gold(I)-Catalyzed 1,5-Hydride Shift/ Cyclization Sequence. J. Am. Chem. Soc. 2010, 132, 3543.

2) Jurberg, I.D.; Gagosz, F.; Zard, S.*; An Unusual Approach to Branched 3-Alkynylamides and to 1,5-Dihydropyrrol-2-ones. Org. Lett. 2010, 12, 416.

1) Istrate, F.; Buzas, A.; Jurberg, I. D.; Odabachian, Y.; Gagosz, F.*; Synthesis of Functionalized Oxazolones by a Sequence of Cu(II)- and Au(I)-Catalyzed Transformations. Org. Lett. 2008, 10, 925.