Claudio Santi - Publications

Affiliations: 
Dept. Pharmaceutical Sciences University of Perugia 
Area:
organic chemistry, stereoselective synthesis, selenium chemistry, biorganic chemistry, green chemistry

198 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Noè R, Inglese N, Romani P, Serafini T, Paoli C, Calciolari B, Fantuz M, Zamborlin A, Surdo NC, Spada V, Spacci M, Volta S, Ermini ML, Di Benedetto G, Frusca V, ... Santi C, et al. Organic Selenium induces ferroptosis in pancreatic cancer cells. Redox Biology. 68: 102962. PMID 38029455 DOI: 10.1016/j.redox.2023.102962  0.596
2023 di Vito R, Acito M, Fatigoni C, Schiesser CH, Davies MJ, Mangiavacchi F, Villarini M, Santi C, Moretti M. Genotoxicity assessment of 1,4-Anhydro-4-seleno-D-talitol (SeTal) in human liver HepG2 and HepaRG cells. Toxicology. 153663. PMID 37924933 DOI: 10.1016/j.tox.2023.153663  0.749
2023 Zeppilli D, Madabeni A, Sancineto L, Bagnoli L, Santi C, Orian L. Role of Group 12 Metals in the Reduction of HO by Santi's Reagent: A Computational Mechanistic Investigation. Inorganic Chemistry. 62: 17288-17298. PMID 37769326 DOI: 10.1021/acs.inorgchem.3c02568  0.612
2023 Palomba M, Dias IFC, Cocchioni M, Marini F, Santi C, Bagnoli L. Vinylation of -Heteroarenes through Addition/Elimination Reactions of Vinyl Selenones. Molecules (Basel, Switzerland). 28. PMID 37630278 DOI: 10.3390/molecules28166026  0.587
2023 Benedetto Tiz D, Bagnoli L, Rosati O, Marini F, Sancineto L, Santi C. Top Selling (2026) Small Molecule Orphan Drugs: A Journey into Their Chemistry. International Journal of Molecular Sciences. 24. PMID 36674441 DOI: 10.3390/ijms24020930  0.659
2022 di Vito R, Levorato S, Fatigoni C, Acito M, Sancineto L, Traina G, Villarini M, Santi C, Moretti M. In vitro toxicological assessment of PhSeZnCl in human liver cells. Toxicological Research. 39: 105-114. PMID 36721677 DOI: 10.1007/s43188-022-00148-y  0.581
2022 Benedetto Tiz D, Bagnoli L, Rosati O, Marini F, Santi C, Sancineto L. FDA-Approved Small Molecules in 2022: Clinical Uses and Their Synthesis. Pharmaceutics. 14. PMID 36432728 DOI: 10.3390/pharmaceutics14112538  0.689
2022 Scimmi C, Sancineto L, Drabowicz J, Santi C. New Insights into Green Protocols for Oxidative Depolymerization of Lignin and Lignin Model Compounds. International Journal of Molecular Sciences. 23. PMID 35457195 DOI: 10.3390/ijms23084378  0.631
2022 Grześ PA, Monti B, Wawrusiewicz-Kurylonek N, Bagnoli L, Sancineto L, Jastrzebska I, Santi C. Simple Zn-Mediated Seleno- and Thio-Functionalization of Steroids at C-1 Position. International Journal of Molecular Sciences. 23. PMID 35328446 DOI: 10.3390/ijms23063022  0.794
2022 Benedetto Tiz D, Bagnoli L, Rosati O, Marini F, Sancineto L, Santi C. New Halogen-Containing Drugs Approved by FDA in 2021: An Overview on Their Syntheses and Pharmaceutical Use. Molecules (Basel, Switzerland). 27. PMID 35268744 DOI: 10.3390/molecules27051643  0.678
2022 Azeredo JB, Penteado F, Nascimento V, Sancineto L, Braga AL, Lenardao EJ, Santi C. "Green Is the Color": An Update on Ecofriendly Aspects of Organoselenium Chemistry. Molecules (Basel, Switzerland). 27. PMID 35268698 DOI: 10.3390/molecules27051597  0.781
2022 Yano de Albuquerque D, Teixeira WKO, Sacramento MD, Alves D, Santi C, Schwab RS. Palladium-Catalyzed Carbonylative Synthesis of Aryl Selenoesters Using Formic Acid as an CO Source. The Journal of Organic Chemistry. 87: 595-605. PMID 34962405 DOI: 10.1021/acs.joc.1c02608  0.369
2021 Sancineto L, Ostacolo C, Ortega-Alarcon D, Jimenez-Alesanco A, Ceballos-Laita L, Vega S, Abian O, Velazquez-Campoy A, Moretti S, Dabrowska A, Botwina P, Synowiec A, Kula-Pacurar A, Pyrc K, Iraci N, ... Santi C, et al. l-Arginine Improves Solubility and ANTI SARS-CoV-2 Mpro Activity of Rutin but Not the Antiviral Activity in Cells. Molecules (Basel, Switzerland). 26. PMID 34641606 DOI: 10.3390/molecules26196062  0.597
2021 Santi C, Scimmi C, Sancineto L. Ebselen and Analogues: Pharmacological Properties and Synthetic Strategies for Their Preparation. Molecules (Basel, Switzerland). 26. PMID 34299505 DOI: 10.3390/molecules26144230  0.609
2021 Mangiavacchi F, Botwina P, Menichetti E, Bagnoli L, Rosati O, Marini F, Fonseca SF, Abenante L, Alves D, Dabrowska A, Kula-Pacurar A, Ortega-Alarcon D, Jimenez-Alesanco A, Ceballos-Laita L, Vega S, ... ... Santi C, et al. Seleno-Functionalization of Quercetin Improves the Non-Covalent Inhibition of M and Its Antiviral Activity in Cells against SARS-CoV-2. International Journal of Molecular Sciences. 22. PMID 34208928 DOI: 10.3390/ijms22137048  0.775
2021 Santi M, Sancineto L, Nascimento V, Braun Azeredo J, Orozco EVM, Andrade LH, Gröger H, Santi C. Flow Biocatalysis: A Challenging Alternative for the Synthesis of APIs and Natural Compounds. International Journal of Molecular Sciences. 22. PMID 33498198 DOI: 10.3390/ijms22030990  0.778
2021 Palomba M, De Monte E, Mambrini A, Bagnoli L, Santi C, Marini F. A three-component [3 + 2]-cycloaddition/elimination cascade for the synthesis of spirooxindole-pyrrolizines. Organic & Biomolecular Chemistry. PMID 33399163 DOI: 10.1039/d0ob02321c  0.61
2020 Mangiavacchi F, Coelho Dias IF, Di Lorenzo I, Grzes P, Palomba M, Rosati O, Bagnoli L, Marini F, Santi C, Lenardao EJ, Sancineto L. Sweet Selenium: Synthesis and Properties of Selenium-Containing Sugars and Derivatives. Pharmaceuticals (Basel, Switzerland). 13. PMID 32859124 DOI: 10.3390/Ph13090211  0.786
2020 Obieziurska-Fabisiak M, Pacuła AJ, Capoccia L, Drogosz-Stachowicz J, Janecka A, Santi C, Ścianowski J. Phenylselanyl Group Incorporation for "Glutathione Peroxidase-Like" Activity Modulation. Molecules (Basel, Switzerland). 25. PMID 32722043 DOI: 10.3390/Molecules25153354  0.343
2020 Abenante L, Padilha NB, Anghinoni JM, Penteado F, Rosati O, Santi C, Silva MS, Lenardão EJ. Arylseleninic acid as a green, bench-stable selenylating agent: synthesis of selanylanilines and 3-selanylindoles. Organic & Biomolecular Chemistry. 18: 5210-5217. PMID 32602500 DOI: 10.1039/D0Ob01073A  0.448
2020 Mangiavacchi F, Crociani L, Sancineto L, Marini F, Santi C. Continuous Bioinspired Oxidation of Sulfides. Molecules (Basel, Switzerland). 25. PMID 32545303 DOI: 10.3390/Molecules25112711  0.802
2020 Nacca FG, Monti B, Lenardão EJ, Evans P, Santi C. A Simple Zinc-Mediated Method for Selenium Addition to Michael Acceptors. Molecules (Basel, Switzerland). 25. PMID 32357472 DOI: 10.3390/Molecules25092018  0.822
2020 Bocchini B, Goldani B, Sousa FSS, Birmann PT, Brüning CA, Lenardão EJ, Santi C, Savegnago L, Alves D. Synthesis and antioxidant activity of new selenium-containing quinolines. Medicinal Chemistry (Shariqah (United Arab Emirates)). PMID 32242787 DOI: 10.2174/1573406416666200403081831  0.43
2020 Begini F, Krasowska D, Jasiak A, Drabowicz J, Santi C, Sancineto L. Continuous flow synthesis of 2,2′-diselenobis(benzoic acid) and derivatives Reaction Chemistry & Engineering. 5: 641-644. DOI: 10.1039/D0Re00012D  0.671
2020 Nascimento V, Cordeiro PS, Arca M, Marini F, Sancineto L, Braga AL, Lippolis V, Iwaoka M, Santi C. Fast and easy conversion of ortho amidoaryldiselenides into the corresponding ebselen-like derivatives driven by theoretical investigations New Journal of Chemistry. 44: 9444-9451. DOI: 10.1039/D0Nj01605E  0.793
2020 Araujo DR, Lima YR, Barcellos AM, Silva MS, Jacob RG, Lenardão EJ, Bagnoli L, Santi C, Perin G. Ultrasound‐Promoted Radical Synthesis of 5‐Methylselanyl‐4,5‐dihydroisoxazoles European Journal of Organic Chemistry. 2020: 586-592. DOI: 10.1002/Ejoc.201901611  0.364
2019 Hayashi S, Nishide T, Nakanishi W, Sancineto L, Santi C. The nature of G⋯E-Y σ(3c-4e) in -Me GCHCHEY (Me G = MeN and MeE; E = O, S, Se and Te; Y = F, Cl, Br, EMe and Me) with contributions from CT and compliance constants in noncovalent G⋯E interactions. Rsc Advances. 9: 39435-39446. PMID 35540683 DOI: 10.1039/c9ra09022c  0.565
2019 Iraci N, Tabarrini O, Santi C, Sancineto L. Corrigendum to "NCp7: targeting a multitask protein for next-generation anti-HIV drug development part 2. Noncovalent inhibitors and nucleic acid binders" [Drug Discov. Today 23(2018) 687-695]. Drug Discovery Today. PMID 31857068 DOI: 10.1016/J.Drudis.2019.12.002  0.607
2019 Krasowska D, Iraci N, Santi C, Drabowicz J, Cieslak M, Kaźmierczak-Barańska J, Palomba M, Królewska-Golińska K, Magiera J, Sancineto L. Diselenides and Benzisoselenazolones as Antiproliferative Agents and Glutathione-S-Transferase Inhibitors. Molecules (Basel, Switzerland). 24. PMID 31405214 DOI: 10.3390/Molecules24162914  0.641
2019 Jastrzebska I, Mellea S, Salerno V, Grzes PA, Siergiejczyk L, Niemirowicz-Laskowska K, Bucki R, Monti B, Santi C. PhSeZnCl in the Synthesis of Steroidal β-Hydroxy-Phenylselenides Having Antibacterial Activity. International Journal of Molecular Sciences. 20. PMID 31032813 DOI: 10.3390/Ijms20092121  0.712
2019 Krasowska D, Begini F, Santi C, Mangiavacchi F, Drabowicz J, Sancineto L. Ultrasound-assisted synthesis of alkali metals diselenides (M2Se2) and their application for the gram-scale preparation of 2,2'-diselenobis(benzoic acid) Arkivoc. 2019: 24-37. DOI: 10.24820/Ark.5550190.P010.981  0.786
2019 Perin G, Nobre P, Mailahn D, Silva M, Barcellos T, Jacob R, Lenardão E, Santi C, Roehrs J. Synthesis of 4-Organoselanyl-1H-pyrazoles: Oxone®-Mediated Electrophilic Cyclization of α,β-Alkynyl Hydrazones by Using Diorganyl Diselenides Synthesis. 51: 2293-2304. DOI: 10.1055/S-0037-1611747  0.426
2019 Hayashi S, Nishide T, Nakanishi W, Sancineto L, Santi C. The nature of G⋯E–Y σ(3c–4e) in o-MenGCH2C6H4EY (MenG = Me2N and MeE; E = O, S, Se and Te; Y = F, Cl, Br, EMe and Me) with contributions from CT and compliance constants in noncovalent G⋯E interactions Rsc Advances. 9: 39435-39446. DOI: 10.1039/C9Ra09022C  0.595
2019 Lippolis V, Santi C. Selenium & tellurium chemistry at the beginning of the 3rd millennium: a celebration of ICCST New Journal of Chemistry. 43: 11032-11033. DOI: 10.1039/C9Nj90092F  0.31
2019 Palomba M, Scarcella E, Sancineto L, Bagnoli L, Santi C, Marini F. Synthesis of Spirooxindole Oxetanes Through a Domino Reaction of 3-Hydroxyoxindoles and Phenyl Vinyl Selenone European Journal of Organic Chemistry. 2019: 5396-5401. DOI: 10.1002/Ejoc.201900499  0.778
2018 Mazzeo G, Longhi G, Abbate S, Mangiavacchi F, Santi C, Han J, Soloshonok VA, Melensi L, Ruzziconi R. Mannich-type addition of 1,3-dicarbonyl compounds to chiral tert-butanesulfinyltrifluoroacetaldimines. Mechanistic aspects and chiroptical studies. Organic & Biomolecular Chemistry. PMID 30393798 DOI: 10.1039/C8Ob02204F  0.812
2018 Iraci N, Tabarrini O, Santi C, Sancineto L. NCp7: targeting a multitask protein for next-generation anti-HIV drug development part 2. Noncovalent inhibitors and nucleic acid binders. Drug Discovery Today. PMID 29326078 DOI: 10.1016/J.Drudis.2018.01.022  0.618
2018 Sancineto L, Iraci N, Tabarrini O, Santi C. NCp7: targeting a multitasking protein for next-generation anti-HIV drug development part 1: covalent inhibitors. Drug Discovery Today. 23: 260-271. PMID 29107765 DOI: 10.1016/J.Drudis.2017.10.017  0.607
2018 Sancineto L, Monti B, Merlino O, Rosati O, Santi C. Q-Tube © assisted MCRs for the synthesis of 2,3-dihydroquinazolin-4(1H)-ones Arkivoc. 2018: 270-278. DOI: 10.24820/Ark.5550190.P010.506  0.746
2018 Santi C, Capoccia L, Monti B. Zinc-Selenium reagents in organic synthesis Physical Sciences Reviews. 3. DOI: 10.1515/Psr-2017-0129  0.707
2018 Thurow S, Penteado F, Perin G, Alves D, Santi C, Monti B, Schiesser CH, Barcellos T, Lenardão EJ. Selenium dioxide-promoted selective synthesis of mono- and bis-sulfenylindoles Organic Chemistry Frontiers. 5: 1983-1991. DOI: 10.1039/C8Qo00360B  0.689
2018 Palomba M, Sancineto L, Marini F, Santi C, Bagnoli L. A domino approach to pyrazino- indoles and pyrroles using vinyl selenones Tetrahedron. 74: 7156-7163. DOI: 10.1016/J.Tet.2018.10.044  0.727
2018 Mangiavacchi F, Mollari L, Bagnoli L, Marini F, Santi C. Condensation of 2-aminomethylaniline with aldehydes and ketones for the fast one-pot synthesis of a library of 1,2,3,4-tetrahydroquinazolines under flow conditions Chemistry of Heterocyclic Compounds. 54: 478-481. DOI: 10.1007/S10593-018-2292-0  0.817
2018 Palomba M, Trappetti F, Bagnoli L, Santi C, Marini F. Oxone-Mediated Oxidation of Vinyl Selenides in Water European Journal of Organic Chemistry. 2018: 3914-3919. DOI: 10.1002/Ejoc.201800498  0.499
2018 Penteado F, Monti B, Sancineto L, Perin G, Jacob RG, Santi C, Lenardão EJ. Ultrasound‐Assisted Multicomponent Reactions, Organometallic and Organochalcogen Chemistry Asian Journal of Organic Chemistry. 7: 2368-2385. DOI: 10.1002/Ajoc.201800477  0.784
2017 Santi C, Tomassini C, Sancineto L. Organic Diselenides: Versatile Reagents, Precursors, and Intriguing Biologically Active Compounds. Chimia. 71: 592-595. PMID 30188290 DOI: 10.2533/Chimia.2017.592  0.728
2017 Bartolini D, Sancineto L, Fabro de Bem A, Tew KD, Santi C, Radi R, Toquato P, Galli F. Selenocompounds in Cancer Therapy: An Overview. Advances in Cancer Research. 136: 259-302. PMID 29054421 DOI: 10.1016/Bs.Acr.2017.07.007  0.631
2017 Galant LS, Braga MM, de Souza D, de Bem AF, Sancineto L, Santi C, da Rocha JBT. Induction of reactive oxygen species by diphenyl diselenide is preceded by changes in cell morphology and permeability in Saccharomyces cerevisiae. Free Radical Research. 1-12. PMID 28840761 DOI: 10.1080/10715762.2017.1355054  0.623
2017 Sancineto L, Pinto Vargas J, Monti B, Arca M, Lippolis V, Perin G, Lenardao EJ, Santi C. Atom Efficient Preparation of Zinc Selenates for the Synthesis of Selenol Esters under "On Water" Conditions. Molecules (Basel, Switzerland). 22. PMID 28594361 DOI: 10.3390/Molecules22060953  0.788
2017 Mazzeo G, Longhi G, Abbate S, Palomba M, Bagnoli L, Marini F, Santi C, Han J, Soloshonok VA, Di Crescenzo E, Ruzziconi R. Solvent-free, uncatalyzed asymmetric "ene" reactions of N-tert-butylsulfinyl-3,3,3-trifluoroacetaldimines: a general approach to enantiomerically pure α-(trifluoromethyl)tryptamines. Organic & Biomolecular Chemistry. PMID 28436530 DOI: 10.1039/C7Ob00670E  0.623
2017 Perin G, Barcellos AM, Luz EQ, Borges EL, Jacob RG, Lenardão EJ, Sancineto L, Santi C. Green Hydroselenation of Aryl Alkynes: Divinyl Selenides as a Precursor of Resveratrol. Molecules (Basel, Switzerland). 22. PMID 28230754 DOI: 10.3390/Molecules22020327  0.721
2017 Cerra B, Mangiavacchi F, Santi C, Lozza AM, Gioiello A. Selective continuous flow synthesis of hydroxy lactones from alkenoic acids Reaction Chemistry & Engineering. 2: 467-471. DOI: 10.1039/C7Re00083A  0.787
2017 Fiorito S, Epifano F, Preziuso F, Taddeo VA, Santi C, Genovese S. New insights into the seleniranium ion promoted cyclization of prenyl and propenylbenzene aryl ethers Tetrahedron Letters. 58: 371-374. DOI: 10.1016/J.Tetlet.2016.12.044  0.428
2017 Kamińska K, Wojaczyńska E, Santi C, Sancineto L, Francesca Pensa M, Kochel A, Wieczorek R, Wojaczyński J, Slupski G. An enantiopure diselenide based on a chiral bicyclic backbone—synthesis and configuration assignment Tetrahedron: Asymmetry. 28: 1367-1372. DOI: 10.1016/J.Tetasy.2017.08.008  0.677
2017 Lima DB, Penteado F, Vieira MM, Alves D, Perin G, Santi C, Lenardão EJ. α-Keto Acids as Acylating Agents in the Synthesis of 2-Substituted Benzothiazoles and Benzoselenazoles European Journal of Organic Chemistry. 2017: 3830-3836. DOI: 10.1002/Ejoc.201700648  0.455
2017 Sancineto L, Mangiavacchi F, Tidei C, Bagnoli L, Marini F, Gioiello A, Scianowski J, Santi C. Selenium-Catalyzed Oxacyclization of Alkenoic Acids and Alkenols Asian Journal of Organic Chemistry. 6: 988-992. DOI: 10.1002/Ajoc.201700193  0.813
2016 Santi C, Jacob RG, Monti B, Bagnoli L, Sancineto L, Lenardão EJ. Water and Aqueous Mixtures as Convenient Alternative Media for Organoselenium Chemistry. Molecules (Basel, Switzerland). 21. PMID 27827970 DOI: 10.3390/Molecules21111482  0.773
2016 Sancineto L, Piccioni M, De Marco S, Pagiotti R, Nascimento V, Braga AL, Santi C, Pietrella D. Diphenyl diselenide derivatives inhibit microbial biofilm formation involved in wound infection. Bmc Microbiology. 16: 220. PMID 27654924 DOI: 10.1186/S12866-016-0837-X  0.772
2016 Palomba M, Rossi L, Sancineto L, Tramontano E, Corona A, Bagnoli L, Santi C, Pannecouque C, Tabarrini O, Marini F. A new vinyl selenone-based domino approach to spirocyclopropyl oxindoles endowed with anti-HIV RT activity. Organic & Biomolecular Chemistry. 14: 2015-24. PMID 26754878 DOI: 10.1039/C5Ob02451J  0.722
2016 Tomassini C, Sarra FD, Monti B, Sancineto L, Bagnoli L, Marini F, Santi C. Kinetic resolution of 2-carbomethoxy-3-alkenols through a stereoselective cyclofunctionalization promoted by an enantiomerically pure electrophilic selenium reagent Arkivoc. 2017. DOI: 10.3998/Ark.5550190.P009.826  0.81
2016 Pacuła AJ, Mangiavacchi F, Sancineto L, J. Lenardão E, Ścianowski J, Santi C. An Update on “Selenium Containing Compounds from Poison to Drug Candidates: A Review on the GPx-like Activity” Current Chemical Biology. 9: 97-112. DOI: 10.2174/2212796810666160120220725  0.769
2016 Bellino G, Scisciani M, Vargas JP, Sancineto L, Bagnoli L, Marini F, Lüdtke DS, Lenardao EJ, Santi C. Reaction of Acyl Chlorides withIn SituFormed Zinc Selenolates: Synthesis of SelenoestersversusRing-Opening Reaction of Tetrahydrofuran Journal of Chemistry. 2016: 1-8. DOI: 10.1155/2016/2849140  0.822
2016 Palomba M, Bagnoli L, Marini F, Santi C, Sancineto L. Recent advances in the chemistry of vinylchalcogenides Phosphorus, Sulfur and Silicon and the Related Elements. 191: 235-244. DOI: 10.1080/10426507.2015.1067212  0.684
2016 Fiorito S, Epifano F, Taddeo V, Genovese S, Sancineto L, Santi C. Preliminary investigations on seleno-analogues of plant oxyprenylated secondary metabolites Planta Medica. 81: S1-S381. DOI: 10.1055/S-0036-1596776  0.601
2016 Perin G, Barcellos A, Peglow TJ, Nobre PC, Cargnelutti R, Lenardão EJ, Marini F, Santi C. Tellurium-promoted stereoselective hydrodebromination of 1,1-dibromoalkenes: synthesis of (E)-bromoalkenes Rsc Adv.. 6: 103657-103661. DOI: 10.1039/C6Ra24295B  0.616
2016 Penteado F, Vieira MM, Perin G, Alves D, Jacob RG, Santi C, Lenardão EJ. Niobium-promoted reaction of α-phenylglyoxylic acid with ortho-functionalized anilines: synthesis of 2-arylbenzothiazoles and 3-aryl-2H-benzo[b][1,4]benzoxazin-2-ones Green Chemistry. 18: 6675-6680. DOI: 10.1039/C6Gc02495E  0.435
2016 Boualy B, El Houssame S, Sancineto L, Santi C, Ait Ali M, Stoeckli-Evans H, El Firdoussi L. A mild and efficient method for the synthesis of a new optically active diallyl selenide and its catalytic activity in the allylic chlorination of natural terpenes New Journal of Chemistry. 40: 3395-3399. DOI: 10.1039/C5Nj02797G  0.69
2016 Palomba M, Vinti E, Marini F, Santi C, Bagnoli L. Synthesis of oxazino[4,3- a ]indoles by domino addition-cyclization reactions of (1 H -indol-2-yl)methanols and vinyl selenones in the presence of 18-crown-6 Tetrahedron. 72: 7059-7064. DOI: 10.1016/J.Tet.2016.09.045  0.634
2016 Sancineto L, Tidei C, Bagnoli L, Marini F, Lippolis V, Arca M, Lenardão EJ, Santi C. Synthesis of Thiol Esters Using PhSZnBr as Sulfenylating Agent: A DFT-Guided Optimization of Reaction Conditions European Journal of Organic Chemistry. 2016: 2999-3005. DOI: 10.1002/Ejoc.201600366  0.813
2015 Achibat H, AlOmari NA, Messina F, Sancineto L, Khouili M, Santi C. Organoselenium Compounds as Phytochemicals from the Natural Kingdom. Natural Product Communications. 10: 1885-92. PMID 26749817 DOI: 10.1177/1934578X1501001119  0.765
2015 Sancineto L, Mariotti A, Bagnoli L, Marini F, Desantis J, Iraci N, Santi C, Pannecouque C, Tabarrini O. Design and Synthesis of DiselenoBisBenzamides (DISeBAs) as Nucleocapsid Protein 7 (NCp7) Inhibitors with anti-HIV Activity. Journal of Medicinal Chemistry. PMID 26613134 DOI: 10.1021/Acs.Jmedchem.5B01183  0.7
2015 Vieira BM, Thurow S, Brito JS, Perin G, Alves D, Jacob RG, Santi C, Lenardão EJ. Sonochemistry: An efficient alternative to the synthesis of 3-selanylindoles using CuI as catalyst. Ultrasonics Sonochemistry. 27: 192-9. PMID 26186837 DOI: 10.1016/J.Ultsonch.2015.05.012  0.39
2015 Bartolini D, Commodi J, Piroddi M, Incipini L, Sancineto L, Santi C, Galli F. Glutathione S-transferase pi expression regulates the Nrf2-dependent response to hormetic diselenides. Free Radical Biology & Medicine. 88: 466-480. PMID 26151571 DOI: 10.1016/J.Freeradbiomed.2015.06.039  0.624
2015 Sancineto L, Tidei C, Bagnoli L, Marini F, Lenardão EJ, Santi C. Selenium Catalyzed Oxidation of Aldehydes: Green Synthesis of Carboxylic Acids and Esters. Molecules (Basel, Switzerland). 20: 10496-510. PMID 26060915 DOI: 10.3390/Molecules200610496  0.829
2015 Vieira AA, Azeredo JB, Godoi M, Santi C, Da Silva Júnior EN, Braga AL. Catalytic chalcogenylation under greener conditions: A solvent-free sulfur- and seleno-functionalization of olefins via I2/DMSO oxidant system Journal of Organic Chemistry. 80: 2120-2127. PMID 25607341 DOI: 10.1021/Jo502621A  0.424
2015 Bartolini D, Piroddi M, Tidei C, Giovagnoli S, Pietrella D, Manevich Y, Tew KD, Giustarini D, Rossi R, Townsend DM, Santi C, Galli F. Reaction kinetics and targeting to cellular glutathione S-transferase of the glutathione peroxidase mimetic PhSeZnCl and its D,L-polylactide microparticle formulation. Free Radical Biology & Medicine. 78: 56-65. PMID 25452145 DOI: 10.1016/J.Freeradbiomed.2014.10.008  0.776
2015 Sancineto L, Palomba M, Bagnoli L, Marini F, Santi C. Advances in Electrophilic Organochalcogen Reagents Current Organic Chemistry. 20: 122-135. DOI: 10.2174/1385272819666150724233204  0.714
2015 Lopes EF, Gonçalves LC, Vinueza JCG, Jacob RG, Perin G, Santi C, Lenardão EJ. DES as a green solvent to prepare 1,2-bis-organylseleno alkenes. Scope and limitations Tetrahedron Letters. 56: 6890-6895. DOI: 10.1016/J.Tetlet.2015.10.095  0.457
2014 Nascimento V, Ferreira NL, Canto RFS, Schott KL, Waczuk EP, Sancineto L, Santi C, Rocha JBT, Braga AL. Synthesis and biological evaluation of new nitrogen-containing diselenides European Journal of Medicinal Chemistry. 87: 131-139. PMID 25244678 DOI: 10.1016/J.Ejmech.2014.09.022  0.807
2014 Santoro S, Azeredo JB, Nascimento V, Sancineto L, Braga AL, Santi C. The green side of the moon: Ecofriendly aspects of organoselenium chemistry Rsc Advances. 4: 31521-31535. DOI: 10.1039/C4Ra04493B  0.784
2014 Tidei C, Sancineto L, Bagnoli L, Battistelli B, Marini F, Santi C. A recyclable biphasic system for stereoselective and easily handled hydrochalcogenations European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201402668  0.812
2013 Santoro S, Superchi S, Messina F, Santoro E, Rosati O, Santi C, Marcotullio MC. Agarsenone, a Cadinane Sesquiterpenoid from Commiphora erythraea. Journal of Natural Products. 76: 1254-9. PMID 23844767 DOI: 10.1021/Np400114B  0.633
2013 Santi C, Tidei C, Scalera C, Piroddi M, Galli F. Selenium Containing Compounds from Poison to Drug Candidates: A Review on the GPx-like Activity Current Chemical Biology. 7: 25-36. DOI: 10.2174/2212796811307010003  0.782
2013 Propersi S, Tidei C, Bagnoli L, Marini F, Testaferri L, Santi C. " On-water " thiolysis of epoxides promoted by PhSZnBr Journal of Sulfur Chemistry. 34: 671-676. DOI: 10.1080/17415993.2013.781604  0.828
2013 Santi C, Galli F, Piroddi M, Tidei C. Thiols oxidation for the evaluation of Gpx-like activity Phosphorus, Sulfur and Silicon and the Related Elements. 188: 507-508. DOI: 10.1080/10426507.2012.727924  0.751
2013 Sternativo S, Battistelli B, Bagnoli L, Santi C, Testaferri L, Marini F. Synthesis of γ-lactams via a domino Michael addition/cyclization reaction of vinyl selenone with substituted amides Tetrahedron Letters. 54: 6755-6757. DOI: 10.1016/J.Tetlet.2013.10.004  0.827
2013 Bagnoli L, Casini S, Marini F, Santi C, Testaferri L. Vinyl selenones: Annulation agents for the synthesis of six-membered benzo-1,4-heterocyclic compounds Tetrahedron. 69: 481-486. DOI: 10.1016/J.Tet.2012.11.036  0.627
2013 Harrad MA, Boualy B, El Firdoussi L, Mehdi A, Santi C, Giovagnoli S, Nocchetti M, Ait Ali M. Colloidal nickel(0)-carboxymethyl cellulose particles: A biopolymer-inorganic catalyst for hydrogenation of nitro-aromatics and carbonyl compounds Catalysis Communications. 32: 92-100. DOI: 10.1016/J.Catcom.2012.11.025  0.372
2013 Bagnoli L, Casini S, Marini F, Santi C, Testaferri L. ChemInform Abstract: Vinyl Selenones: Annulation Agents for the Synthesis of Six-Membered Benzo-1,4-heterocyclic Compounds. Cheminform. 44: no-no. DOI: 10.1002/CHIN.201324163  0.537
2013 Santi C, Tidei C. Electrophilic Selenium/Tellurium Reagents: Reactivity and their Contribution to Green Chemistry Patai's Chemistry of Functional Groups. DOI: 10.1002/9780470682531.Pat0720  0.835
2012 Santi C, Battistelli B, Testaferri L, Tiecco M. On water preparation of phenylselenoesters Green Chemistry. 14: 1277. DOI: 10.1039/C2Gc16541D  0.809
2012 Tidei C, Piroddi M, Galli F, Santi C. Oxidation of thiols promoted by PhSeZnCl Tetrahedron Letters. 53: 232-234. DOI: 10.1016/J.Tetlet.2011.11.025  0.771
2012 Santi C, Di Lorenzo R, Tidei C, Bagnoli L, Wirth T. Stereoselective selenium catalyzed dihydroxylation and hydroxymethoxylation of alkenes Tetrahedron. 68: 10530-10535. DOI: 10.1016/J.Tet.2012.08.078  0.828
2012 Legnaioli⁎ S, Piroddi M, Tidei C, Santi C, Galli F. PhSeZnCl: a new seleno-organic compound with glutathione peroxidase-like activity Free Radical Biology and Medicine. 53: S147. DOI: 10.1016/J.Freeradbiomed.2012.08.308  0.758
2012 Legnaioli⁎ S, Piroddi M, Tidei C, Santi C, Galli F. Targeting the GSTP-dependent control of cell kinases and apoptosis with PhSeZnCl: a new seleno-organic drug Free Radical Biology and Medicine. 53: S112. DOI: 10.1016/J.Freeradbiomed.2012.08.235  0.739
2011 Senatore M, Lattanzi A, Santoro S, Santi C, Della Sala G. A general phosphoric acid-catalyzed desymmetrization of meso-aziridines with silylated selenium nucleophiles. Organic & Biomolecular Chemistry. 9: 6205-7. PMID 21796320 DOI: 10.1039/C1Ob05837A  0.732
2011 Battistelli B, Lorenzo T, Tiecco M, Santi C. “On-Water” Michael-Type Addition Reactions Promoted by PhSeZnCl European Journal of Organic Chemistry. 2011: 1848-1851. DOI: 10.1002/Ejoc.201100045  0.813
2010 Santi C, Santoro S, Battistelli B. Organoselenium Compounds as Catalysts in Nature and Laboratory Current Organic Chemistry. 14: 2442-2462. DOI: 10.2174/138527210793358231  0.779
2010 Santi C, Santoro S, Battistelli B, Gjoka B, Si C, Testaferri L, Tiecco M. Oxidation of Alkynes in Aqueous Media Catalyzed by Diphenyl Diselenide Synlett. 2010: 1402-1406. DOI: 10.1055/S-0029-1219817  0.804
2010 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. ChemInform Abstract: Asymmetric Synthesis of Thioamido Selenides. A Simple Synthetic Route to Enantiopure Thiazolines. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200236174  0.751
2010 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. ChemInform Abstract: Optically Active Isoxazolidines and 1,3-Amino Alcohols by Asymmetric Selenocyclization Reactions of O-Allyl Oximes. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200234143  0.703
2010 Tiecco M, Testaferri L, Bagnoli L, Purgatorio V, Temperini A, Marini F, Santi C. ChemInform Abstract: Efficient Asymmetric Selenocyclizations of Alkenyl Oximes into Cyclic Nitrones and 1,2-Oxazines Promoted by Sulfur Containing Diselenides. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200234045  0.738
2010 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. ChemInform Abstract: Oxidation of Diphenyl Diselenide with 2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ). A New Method for the Electrophilic Phenylselenenylation of Alkenes under Mild Conditions. Cheminform. 33: no-no. DOI: 10.1002/CHIN.200210155  0.703
2010 Tiecco M, Testaferri L, Marini F, Sternativo S, Bagnoli L, Santi C, Temperini A. ChemInform Abstract: A Sulfur-Containing Diselenide as an Efficient Chiral Reagent in Asymmetric Selenocyclization Reactions. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200150034  0.758
2010 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. ChemInform Abstract: A New Synthesis of α-Phenylseleno Esters and Acids from Terminal Alkynes. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200133207  0.734
2010 Tiecco M, Testaferri L, Bagnoli L, Marini F, Temperini A, Tomassini C, Santi C. ChemInform Abstract: Efficient Asymmetric Selenomethoxylation and Selenohydroxylation of Alkenes with a New Sulfur Containing Chiral Diselenide. Cheminform. 31: no-no. DOI: 10.1002/CHIN.200036185  0.731
2010 Tiecco M, Testaferri L, Bagnoli L, Marini F, Temperini A, Tomassini C, Santi C. ChemInform Abstract: Electrophilic 2-Thienylselenenylation of Thiophene. Preparation of Oligo(seleno-2,5-thienylenes). Cheminform. 31: no-no. DOI: 10.1002/CHIN.200033170  0.724
2010 Tiecco M, Testaferri L, Marini F, Santi C, Bagnoli L, Temperini A. ChemInform Abstract: Asymmetric Oxyselenenylation-Deselenenylation Reactions of Alkenes Induced by Camphor Diselenide and Ammonium Persulfate. A Convenient One-Pot Synthesis of Enantiomerically Enriched Allylic Alcohols and Ethers. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199933092  0.745
2010 Tiecco M, Testaferri L, Temperini A, Marini F, Bagnoli L, Santi C. ChemInform Abstract: Selenium Promoted Stereospecific One-Pot Conversion of Cinnamyl Derivatives into Oxazolines. A Simple Synthetic Route to Racemic Taxol Side Chain. Cheminform. 30: no-no. DOI: 10.1002/CHIN.199931153  0.727
2010 TIECCO M, TESTAFERRI L, TEMPERINI A, BAGNOLI L, MARINI F, SANTI C. ChemInform Abstract: Electrophilic Azido Selenenylation of Alkenes. A Simple Synthetic Route to Racemic Taxol Side Chain. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199842173  0.71
2010 TIECCO M, TESTAFERRI L, SANTI C, MARINI F, BAGNOLI L, TEMPERINI A. ChemInform Abstract: Asymmetric Selenomethoxylation of Alkenes with Camphorselenenyl Sulfate. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199830209  0.725
2010 TIECCO M, TESTAFERRI L, MARINI F, TEMPERINI A, BAGNOLI L, SANTI C. ChemInform Abstract: One-Pot Conversion of Alkenes into Oxazolines and Oxazolidin-2-ones Promoted by Diphenyl Diselenide. Cheminform. 29: no-no. DOI: 10.1002/CHIN.199808109  0.734
2010 TIECCO M, TESTAFERRI L, MARINI F, SANTI C, BAGNOLI L, TEMPERINI A. ChemInform Abstract: Factors Controlling the Selenium-Induced Cyclizations of Alkenyl Hydrazines to Pyridazine or Pyrrolidinamine Derivatives. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199748045  0.695
2010 TIECCO M, TESTAFERRI L, MARINI F, SANTI C, BAGNOLI L, TEMPERINI A. ChemInform Abstract: Pyrrolidinamine, Piperidinamine and Tetrahydropyridazine Derivatives from Selenium Promoted Cyclization of Alkenyl Phenylhydrazones. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199742212  0.736
2010 TIECCO M, TESTAFERRI L, MARINI F, BAGNOLI L, SANTI C, TEMPERINI A. ChemInform Abstract: Phenylselenenyl Sulfate Induced Cyclization of Allylhydrazines. Synthesis of Pyrazole Derivatives. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199729109  0.748
2010 TIECCO M, TESTAFERRI L, BAGNOLI L, MARINI F, SANTI C, TEMPERINI A. ChemInform Abstract: Selenium-Catalyzed Conversion of δ-Phenyl-γ-alkenyl Oximes into 2-Phenylpyridines. Cheminform. 28: no-no. DOI: 10.1002/CHIN.199717134  0.743
2010 TIECCO M, TESTAFERRI L, TINGOLI M, BAGNOLI L, MARINI F, SANTI C, TEMPERINI A. ChemInform Abstract: Production and Reactivity of New Organoselenium Intermediates. Formation of Carbon-Oxygen and Carbon-Nitrogen Bonds Cheminform. 28: no-no. DOI: 10.1002/CHIN.199709263  0.674
2009 Freudendahl DM, Santoro S, Shahzad SA, Santi C, Wirth T. Green chemistry with selenium reagents: development of efficient catalytic reactions. Angewandte Chemie (International Ed. in English). 48: 8409-11. PMID 19802863 DOI: 10.1002/Anie.200903893  0.746
2009 Santi C, Santoro S, Tomassini C, Pascolini F, Testaferri L, Tiecco M. Enantioselective Methoxyselenenylation of α,β-Unsaturated Aldehydes Synlett. 2009: 743-746. DOI: 10.1055/S-0028-1087936  0.788
2009 Santoro S, Battistelli B, Testaferri L, Tiecco M, Santi C. Vinylic Substitutions Promoted by PhSeZnCl: Synthetic and Theoretical Investigations European Journal of Organic Chemistry. 2009: 4921-4925. DOI: 10.1002/Ejoc.200900800  0.82
2009 Santi C, Santoro S, Tomassini C, Pascolini F, Testaferri L, Tiecco M. ChemInform Abstract: Enantioselective Methoxyselenenylation of α,β-Unsaturated Aldehydes. Cheminform. 40. DOI: 10.1002/chin.200932180  0.621
2009 Freudendahl D, Santoro S, Shahzad S, Santi C, Wirth T. Grüne Chemie mit Selenreagentien: Entwicklung effizienter katalytischer Reaktionen Angewandte Chemie. 121: 8559-8562. DOI: 10.1002/Ange.200903893  0.653
2008 Santi C, Tiecco M, Testaferri L, Tomassini C, Santoro S, Bizzoca G. Diastereo and Enantioselective Synthesis of 1,2-Diols Promoted by Electrophilic Selenium Reagents Phosphorus, Sulfur, and Silicon and the Related Elements. 183: 956-960. DOI: 10.1080/10426500801900881  0.807
2008 Tiecco M, Marini F, Testaferri L, Sternativo S, Verme F, Santi C, Bagnoli L, Temperini A. Salen-Chromium Complex Catalyzed Ring Opening ofmeso-Epoxides Synfacts. 2008: 0728-0728. DOI: 10.1055/S-2008-1077847  0.715
2008 Santi C, Santoro S, Testaferri L, Tiecco M. A Simple Zinc-Mediated Preparation of Selenols Synlett. 2008: 1746-1746. DOI: 10.1055/S-2008-1067136  0.795
2008 Tiecco M, Testaferri L, Marini F, Sternativo S, Del Verme F, Santi C, Bagnoli L, Temperini A. Synthesis of enantiomerically enriched β-hydroxy selenides by catalytic asymmetric ring opening of meso-epoxides with (phenylseleno)silanes Tetrahedron. 64: 3337-3342. DOI: 10.1016/J.Tet.2008.01.126  0.762
2008 Santi C, Santoro S, Battistelli B, Testaferri L, Tiecco M. Preparation of the First Bench-Stable Phenyl Selenolate: an Interesting “On Water” Nucleophilic Reagent European Journal of Organic Chemistry. 2008: 5387-5390. DOI: 10.1002/Ejoc.200800869  0.823
2008 Tiecco M, Testaferri L, Marini F, Sternativo S, Del Verme F, Santi C, Bagnoli L, Temperini A. ChemInform Abstract: Synthesis of Enantiomerically Enriched β-Hydroxy Selenides by Catalytic Asymmetric Ring Opening of meso-Epoxides with (Phenylseleno)silanes. Cheminform. 39. DOI: 10.1002/CHIN.200840172  0.742
2008 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Temperini A, Marini F, Santi C. ChemInform Abstract: Selenium-Promoted Synthesis of Enantiopure Pyrrolidines Starting from Chiral Amino Alcohols. Cheminform. 39. DOI: 10.1002/CHIN.200817114  0.717
2008 Tiecco M, Testaferri L, Santi C, Tomassini C, Santoro S, Marini F, Bagnoli L, Temperini A. ChemInform Abstract: Synthesis of Enantiomerically Pure β-Azidoselenides Starting from Natural Terpenes. Cheminform. 39. DOI: 10.1002/CHIN.200814195  0.722
2008 Santoro S, Santi C, Sabatini M, Testaferri L, Tiecco M. Eco-Friendly Olefin Dihydroxylation Catalyzed by Diphenyl Diselenide Advanced Synthesis & Catalysis. 350: 2881-2884. DOI: 10.1002/Adsc.200800571  0.79
2007 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Stereocontrolled synthesis of substituted N-arenesulfonyl azetidines from gamma-(phenylseleno)alkyl arylsulfonamides. Organic & Biomolecular Chemistry. 5: 3510-9. PMID 17943211 DOI: 10.1039/B712861D  0.765
2007 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. A simple synthesis of (R)-3-aminooctanoic acid (D-BAOA) from (S)-1-octyn-3-ol Tetrahedron Letters. 48: 4343-4345. DOI: 10.1016/J.Tetlet.2007.04.115  0.738
2007 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Temperini A, Marini F, Santi C. Selenium promoted synthesis of enantiopure pyrrolidines starting from chiral aminoalcohols Tetrahedron: Asymmetry. 18: 2758-2767. DOI: 10.1016/J.Tetasy.2007.11.003  0.78
2007 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Temperini A, Marini F, Santi C. Organoselenium Mediated Asymmetric Cyclizations. Synthesis of Enantiomerically Pure 1,6-Dioxaspiro[4.4]nonanes. Cheminform. 38. DOI: 10.1016/J.Tetasy.2006.10.021  0.746
2007 Tiecco M, Testaferri L, Santi C, Tomassini C, Santoro S, Marini F, Bagnoli L, Temperini A. Synthesis of enantiomerically pure β-azidoselenides starting from natural terpenes Tetrahedron. 63: 12373-12378. DOI: 10.1016/J.Tet.2007.09.047  0.818
2007 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Intramolecular addition of carbon radicals to aldehydes: synthesis of enantiopure tetrahydrofuran-3-ols Tetrahedron. 63: 5482-5489. DOI: 10.1016/J.Tet.2007.04.047  0.749
2007 Bagnoli L, Tiecco M, Testaferri L, Scarponi C, Temperini A, Marini F, Santi C. Selenium-Promoted Enantioselective Synthesis of Spiroketals Cheminform. 38. DOI: 10.1002/chin.200729238  0.745
2006 Tiecco M, Testaferri L, Bagnoli L, Marini F, Santi C, Temperini A, Scarponi C, Sternativo S, Terlizzi R, Tomassini C. Enantioselective Synthesis of Heterocyclic Compounds Mediated by Organoselenium Reagents Cheminform. 37. DOI: 10.3998/Ark.5550190.0007.715  0.781
2006 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Synthesis of γ- and δ-Lactones from Alkynols. Cheminform. 37. DOI: 10.1055/S-2006-932477  0.769
2006 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Temperini A, Marini F, Santi C. Organoselenium mediated asymmetric cyclizations. Synthesis of enantiomerically pure 1,6-dioxaspiro[4.4]nonanes Tetrahedron: Asymmetry. 17: 2768-2774. DOI: 10.1016/J.TETASY.2006.10.021  0.756
2006 Tiecco M, Testaferri L, Santi C, Tomassini C, Santoro S, Marini F, Bagnoli L, Temperini A, Costantino F. Intramolecular Nonbonding Interactions between Selenium and Sulfur – Spectroscopic Evidence and Importance in Asymmetric Synthesis European Journal of Organic Chemistry. 2006: 4867-4873. DOI: 10.1002/Ejoc.200600517  0.826
2006 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Synthesis of Optically Pure 1,4-Dioxanes from Alkenes Promoted by Organoselenium Reagents Cheminform. 37. DOI: 10.1002/chin.200619261  0.709
2005 Tiecco M, Testaferri L, Marini F, Bagnoli L, Santi C, Temperini A, Sternativo S, Tomassini C. Asymmetric Syntheses Promoted by Organoselenium Reagents Cheminform. 36. DOI: 10.1080/10426500590907462  0.786
2005 Tiecco M, Testaferri L, Marini F, Bagnoli L, Santi C, Temperini A, Sternativo S, Tomassini C. Asymmetric Syntheses Promoted by Organoselenium Reagents Phosphorus, Sulfur, and Silicon and the Related Elements. 180: 729-740. DOI: 10.1080/10426500590907462  0.742
2005 Santi C, Tiecco M, Testaferri L, Tomassini C, Marini F, Bagnoli L, Temperini A. Kinetic Resolution of Allylic Alcohols Promoted by Electrophilic Selenium Reagents. Cheminform. 36. DOI: 10.1080/10426500590906355  0.712
2005 Santi C, Tiecco M, Testaferri L, Tomassini C, Marini F, Bagnoli L, Temperini A. Kinetic Resolution of Allylic Alcohols Promoted by Electrophilic Selenium Reagents Phosphorus, Sulfur, and Silicon and the Related Elements. 180: 1071-1075. DOI: 10.1080/10426500590906355  0.679
2005 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Short Synthesis of (R)- and (S)-4-Amino-3-hydroxybutyric Acid (GABOB). Cheminform. 36. DOI: 10.1055/S-2005-861783  0.72
2005 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Short Synthesis of (R)- and (S)-4-Amino-3-Hydroxybutyric Acid (GABOB) Synthesis. 2005: 579-582. DOI: 10.1055/S-2005-861783  0.693
2005 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Synthesis of Selenoxides by Oxidation of Selenides with Superoxide Radical Anions and 2-Nitrobenzenesulfonyl Chloride. Cheminform. 36. DOI: 10.1016/J.Tetlet.2005.05.122  0.74
2005 Tiecco M, Testaferri L, Temperini A, Terlizzi R, Bagnoli L, Marini F, Santi C. Synthesis of selenoxides by oxidation of selenides with superoxide radical anions and 2-nitrobenzenesulfonyl chloride Tetrahedron Letters. 46: 5165-5168. DOI: 10.1016/J.TETLET.2005.05.122  0.707
2005 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Purgatorio V, Temperini A, Marini F, Santi C. Synthesis of Enantiomerically Pure Perhydrofuro[2,3-b]furans. Cheminform. 36. DOI: 10.1016/J.Tetasy.2005.06.016  0.745
2005 Tiecco M, Testaferri L, Bagnoli L, Scarponi C, Purgatorio V, Temperini A, Marini F, Santi C. Synthesis of enantiomerically pure perhydrofuro[2,3-b]furans Tetrahedron: Asymmetry. 16: 2429-2435. DOI: 10.1016/J.TETASY.2005.06.016  0.706
2005 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Conjugated Additions of Selenium Containing Enolates to Enones - Enantioselective Synthesis of ?-Oxo-?-Seleno Esters and Their Facile Transformations European Journal of Organic Chemistry. 2005: 543-551. DOI: 10.1002/Ejoc.200400686  0.786
2005 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Conjugated Additions of Selenium Containing Enolates to Enones — Enantioselective Synthesis of δ-Oxo-α-Seleno Esters and Their Facile Transformations. Cheminform. 36. DOI: 10.1002/CHIN.200522183  0.739
2004 Tiecco M, Testaferri L, Santi C, Tomassini C, Bonini R, Marini F, Bagnoli L, Temperini A. A chiral electrophilic selenium reagent to promote the kinetic resolution of racemic allylic alcohols. Organic Letters. 6: 4751-3. PMID 15575677 DOI: 10.1021/Ol048001+  0.729
2004 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. Ring-closure reactions through intramolecular displacement of the phenylselenonyl group by nitrogen nucleophiles: a new stereospecific synthesis of N-tosyl and N-benzoyl-1,3-oxazolidin-2-ones from beta-hydroxyalkyl phenyl selenides. Chemistry (Weinheim An Der Bergstrasse, Germany). 10: 1752-64. PMID 15054763 DOI: 10.1002/Chem.200305497  0.75
2004 Tiecco M, Testaferri L, Bagnoli L, Terlizzi R, Temperini A, Marini F, Santi C, Scarponi C. Synthesis of Enantiomerically Pure Perhydrofuro[3,4-b]pyrans and Perhydrofuro[3,4-b]furans. Cheminform. 35. DOI: 10.1016/J.Tetasy.2004.05.009  0.745
2004 Tiecco M, Testaferri L, Bagnoli L, Terlizzi R, Temperini A, Marini F, Santi C, Scarponi C. Synthesis of enantiomerically pure perhydrofuro[3,4-b]pyrans and perhydrofuro[3,4-b]furans Tetrahedron: Asymmetry. 15: 1949-1955. DOI: 10.1016/J.TETASY.2004.05.009  0.679
2004 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Asymmetric aldol reactions from titanium enolates of α-seleno ketones and esters Tetrahedron: Asymmetry. 15: 783-791. DOI: 10.1016/J.Tetasy.2003.12.035  0.765
2004 Tiecco M, Testaferri L, Bagnoli L, Purgatorio V, Temperini A, Marini F, Santi C. Synthesis of enantiomerically pure substituted tetrahydrofurans from epoxides and phenylselenium reagents Tetrahedron: Asymmetry. 15: 405-412. DOI: 10.1016/J.Tetasy.2003.10.042  0.793
2004 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C, Terlizzi R. Synthesis of SubstitutedSe-Phenyl Selenocarboxylates from Terminal Alkynes European Journal of Organic Chemistry. 2004: 3447-3458. DOI: 10.1002/Ejoc.200400177  0.754
2004 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C, Terlizzi R. Synthesis of Substituted Se-Phenyl Selenocarboxylates from Terminal Alkynes. Cheminform. 35. DOI: 10.1002/chin.200449160  0.749
2003 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. Asymmetric azidoselenenylation of alkenes: a key step for the synthesis of enantiomerically enriched nitrogen-containing compounds. Angewandte Chemie (International Ed. in English). 42: 3131-3. PMID 12866098 DOI: 10.1002/Anie.200351229  0.761
2003 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. A New Synthesis of α-Phenylseleno γ- and δ-Lactones from Terminal Alkynes. Cheminform. 34. DOI: 10.1055/S-2003-38359  0.748
2003 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Selenium-promoted synthesis of enantiomerically pure substituted morpholines starting from alkenes and chiral aminoalcohols Tetrahedron: Asymmetry. 14: 2651-2657. DOI: 10.1016/S0957-4166(03)00498-1  0.767
2003 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Synthesis of enantiomerically pure 1,4-dioxanes from alkenes promoted by organoselenium reagents Tetrahedron: Asymmetry. 14: 1095-1102. DOI: 10.1016/S0957-4166(03)00124-1  0.789
2003 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Selenium-Promoted Synthesis of Enantiomerically Pure Substituted Morpholines Starting from Alkenes and Chiral Aminoalcohols. Cheminform. 34. DOI: 10.1002/CHIN.200352175  0.758
2002 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. Preparation of a new chiral non-racemic sulfur-containing diselenide and applications in asymmetric synthesis. Chemistry (Weinheim An Der Bergstrasse, Germany). 8: 1118-24. PMID 11891899 DOI: 10.1002/1521-3765(20020301)8:5<1118::Aid-Chem1118>3.0.Co;2-2  0.791
2002 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. Asymmetric synthesis of thioamido selenides. A simple synthetic route to enantiopure thiazolines Tetrahedron: Asymmetry. 13: 429-435. DOI: 10.1016/S0957-4166(02)00122-2  0.783
2001 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. Oxidation of Diphenyl Diselenide with 2,3-Dichloro-5,6-dicyanobenzoquinone (DDQ). A New Method for the Electrophilic Phenylselenenylation of Alkenes under Mild Conditions Synlett. 2001: 1767-1771. DOI: 10.1055/S-2001-18091  0.714
2001 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. A New Synthesis of α-Phenylseleno Esters and Acids from Terminal Alkynes Synlett. 2001: 0706-0708. DOI: 10.1055/S-2001-13370  0.748
2001 Tiecco M, Testaferri L, Bagnoli L, Purgatorio V, Temperini A, Marini F, Santi C. Efficient asymmetric selenocyclizations of alkenyl oximes into cyclic nitrones and 1,2-oxazines promoted by sulfur containing diselenides Tetrahedron: Asymmetry. 12: 3297-3304. DOI: 10.1016/S0957-4166(02)00013-7  0.778
2001 Tiecco M, Testaferri L, Marini F, Sternativo S, Santi C, Bagnoli L, Temperini A. Optically active isoxazolidines and 1,3-amino alcohols by asymmetric selenocyclization reactions of O-allyl oximes Tetrahedron: Asymmetry. 12: 3053-3059. DOI: 10.1016/S0957-4166(01)00543-2  0.747
2001 Tiecco M, Testaferri L, Marini F, Sternativo S, Bagnoli L, Santi C, Temperini A. A sulfur-containing diselenide as an efficient chiral reagent in asymmetric selenocyclization reactions Tetrahedron: Asymmetry. 12: 1493-1502. DOI: 10.1016/S0957-4166(01)00248-8  0.789
2001 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. ChemInform Abstract: New Nitrogen Containing Chiral Diselenides: Synthesis and Asymmetric Addition Reactions to Olefins. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200119038  0.77
2001 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. ChemInform Abstract: Asymmetric Amidoselenenylation of Alkenes Promoted by Camphorselenenyl Sulfate: A Useful Synthetic Route to Enantiopure Oxazolines. Cheminform. 32: no-no. DOI: 10.1002/CHIN.200109122  0.729
2000 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. New nitrogen containing chiral diselenides: synthesis and asymmetric addition reactions to olefins Tetrahedron: Asymmetry. 11: 4645-4650. DOI: 10.1016/S0957-4166(00)00469-9  0.783
2000 Tiecco M, Testaferri L, Bagnoli L, Marini F, Temperini A, Tomassini C, Santi C. Efficient asymmetric selenomethoxylation and selenohydroxylation of alkenes with a new sulfur containing chiral diselenide Tetrahedron Letters. 41: 3241-3245. DOI: 10.1016/S0040-4039(00)00358-0  0.772
2000 Tiecco M, Testaferri L, Bagnoli L, Marini F, Temperini A, Tomassini C, Santi C. Electrophilic 2-Thienylselenenylation of Thiophene. Preparation of Oligo(seleno-2,5-thienylenes) Tetrahedron. 56: 3255-3260. DOI: 10.1016/S0040-4020(00)00245-3  0.774
2000 Tiecco M, Testaferri L, Santi C, Tomassini C, Marini F, Bagnoli L, Temperini A. Asymmetric Amidoselenenylation of Alkenes Promoted by Camphorselenenyl Sulfate: A Useful Synthetic Route to Enantiopure Oxazolines European Journal of Organic Chemistry. 2000: 3451-3457. DOI: 10.1002/1099-0690(200010)2000:20<3451::Aid-Ejoc3451>3.0.Co;2-Q  0.764
1999 Tiecco M, Testaferri L, Temperini A, Marini F, Bagnoli L, Santi C. Selenium Promoted Stereospecific One-Pot Conversion Of Cinnamyl Derivatives Into Oxazoleses. A Simple Synthetic Route To Racemic Taxol Side Chain Synthetic Communications. 29: 1773-1778. DOI: 10.1080/00397919908086165  0.774
1999 Santi C, Wirth T. Synthesis of non-racemic nitrogen-containing diselenides as efficient precursor catalysts in the diethylzinc addition to benzaldehyde Tetrahedron: Asymmetry. 10: 1019-1023. DOI: 10.1016/S0957-4166(99)00090-7  0.578
1999 Tiecco M, Testaferri L, Marini F, Santi C, Bagnoli L, Temperini A. Asymmetric oxyselenenylation–deselenenylation reactions of alkenes induced by camphor diselenide and ammonium persulfate. A convenient one-pot synthesis of enantiomerically enriched allylic alcohols and ethers Tetrahedron: Asymmetry. 10: 747-757. DOI: 10.1016/S0957-4166(99)00048-8  0.775
1999 Tiecco M, Testaferri L, Santi C. Catalytic Oxyselenenylation–Deselenenylation Reactions of Alkenes – Stereoselective One-Pot Conversion of 3-Alkenols into 2,5-Dihydrofurans European Journal of Organic Chemistry. 1999: 797-803. DOI: 10.1002/(Sici)1099-0690(199904)1999:4<797::Aid-Ejoc797>3.0.Co;2-O  0.705
1998 Tiecco M, Testaferri L, Temperini A, Bagnoli L, Marini F, Santi C. Electrophilic Azido Selenenylation of Alkenes. A Simple Synthetic Route to Racemic Taxol Side Chain Synthetic Communications. 28: 2167-2179. DOI: 10.1080/00397919808007031  0.75
1998 Santi C, Fragale G, Wirth T. Synthesis Of A New Chiral Nitrogen Containing Diselenide As A Precursor For Selenium Electrophiles Tetrahedron-Asymmetry. 9: 3625-3628. DOI: 10.1016/S0957-4166(98)00380-2  0.588
1998 Tiecco M, Testaferri L, Santi C, Marini F, Bagnoli L, Temperini A. Asymmetric selenomethoxylation of alkenes with camphorselenenyl sulfate Tetrahedron Letters. 39: 2809-2812. DOI: 10.1016/S0040-4039(98)00252-4  0.767
1998 Tiecco M, Testaferri L, Santi C, Marini F, Bagnoli L, Temperini A, Tomassini C. Asymmetric Selenohydroxylation of Alkenes with Camphorselenenyl Sulfate European Journal of Organic Chemistry. 1998: 2275-2277. DOI: 10.1002/(Sici)1099-0690(199811)1998:11<2275::Aid-Ejoc2275>3.0.Co;2-O  0.743
1997 Tiecco M, Testaferri L, Marini F, Temperini A, Bagnoli L, Santi C. One-Pot Conversion of Alkenes into Oxazolines and Oxazolidin-2-Ones Promoted by Diphenyl Diselenide Synthetic Communications. 27: 4131-4140. DOI: 10.1080/00397919708005461  0.771
1997 Tiecco M, Testaferri L, Marini F, Santi C, Bagnoli L, Temperini A. Factors controlling the selenium-induced cyclizations of alkenyl hydrazines to pyridazine or pyrrolidinamine derivatives Tetrahedron. 53: 10591-10602. DOI: 10.1016/S0040-4020(97)00670-4  0.697
1997 Tiecco M, Testaferri L, Marini F, Santi C, Bagnoli L, Temperini A. Pyrrolidinamine, piperidinamine and tetrahydropyridazine derivatives from selenium promoted cyclization of alkenyl phenylhydrazones Tetrahedron. 53: 7311-7318. DOI: 10.1016/S0040-4020(97)00414-6  0.769
1997 Tiecco M, Testaferri L, Marini F, Bagnoli L, Santi C, Temperini A. Phenylselenenyl sulfate induced cyclization of allylhydrazines. Synthesis of pyrazole derivatives Tetrahedron. 53: 4441-4446. DOI: 10.1016/S0040-4020(97)00116-6  0.79
1996 Tiecco M, Testaferri L, Bagnoli L, Marini F, Santi C, Temperini A. Selenium Catalyzed Conversion of d-Phenyl-g-alkenyl Oximes into 2-Phenylpyridines Heterocycles. 43: 2679. DOI: 10.3987/Com-96-7606  0.695
1995 Tiecco M, Testaferri L, Tingoli M, Santi C. New synthesis of isoxazolidines from the selenium-induced cyclization of O-allyl hydroxylamines Tetrahedron Letters. 36: 163-166. DOI: 10.1016/0040-4039(94)02201-L  0.702
1995 Tiecco M, Testaferri L, Tingoli M, Bagnoli L, Santi C. Selenium-induced cyclization of O-allyl oximes as a synthetic route to N-alkyl isoxazolidines Tetrahedron. 51: 1277-1284. DOI: 10.1016/0040-4020(94)01006-L  0.673
1993 Tiecco M, Testaferri L, Tingoli M, Bagnoli L, Santi C. Selenium Catalysed Conversion of β,γ-Unsaturated Acids into Butenolides Synlett. 1993: 798-800. DOI: 10.1055/S-1993-22614  0.645
1993 Tiecco M, Testaferri L, Tingoli M, Bagnoli L, Santi C. Catalytic conversion of β,γ-unsaturated esters, amides and nitriles into γ-alkoxy or γ-hydroxy α,β-unsaturated derivatives induced by persulfate anion oxidation of diphenyl diselenide Journal of the Chemical Society, Chemical Communications. 637-639. DOI: 10.1039/C39930000637  0.678
Show low-probability matches.