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 |
|
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