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Marco Bandini, Ph.D. - Publications

Affiliations: 
Chemistry Università di Bologna, Bologna, Italy 
Area:
Organic Chemistry
Website:
http://www.mbandini-group.com/index.html

139 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 Giovanelli R, Lombardi L, Pedrazzani R, Monari M, Reis MC, López CS, Bertuzzi G, Bandini M. Nickel Catalyzed Carbonylation/Carboxylation Sequence via Double CO Incorporation. Organic Letters. PMID 37669466 DOI: 10.1021/acs.orglett.3c02394  0.301
2022 Lombardi L, Cerveri A, Giovanelli R, Castiñeira Reis M, Silva-Lopez C, Beertuzzi G, Bandini M. Direct Synthesis of α-Aryl-α-Trifluoromethyl Alcohols via Nickel Catalyzed Cross-Electrophile Coupling. Angewandte Chemie (International Ed. in English). PMID 36161744 DOI: 10.1002/anie.202211732  0.365
2022 Pedrazzani R, Pinosa E, Bertuzzi G, Monari M, Lauzon S, Ollevier T, Bandini M. Convenient synthesis of tricyclic N(1)-C(2)-fused oxazino-indolones [Au(I)] catalyzed hydrocarboxylation of allenes. Chemical Communications (Cambridge, England). 58: 8698-8701. PMID 35833468 DOI: 10.1039/d2cc02303b  0.41
2022 Bertuzzi G, Ombrosi G, Bandini M. Regio- and Stereoselective Electrochemical Alkylation of Morita-Baylis-Hillman Adducts. Organic Letters. 24: 4354-4359. PMID 35700274 DOI: 10.1021/acs.orglett.2c01529  0.321
2021 Liu Y, Battaglioli S, Lombardi L, Menichetti A, Valenti G, Montalti M, Bandini M. Visible-Light Photoredox Catalyzed Dehydrogenative Synthesis of Allylic Carboxylates from Styrenes. Organic Letters. 23: 4441-4446. PMID 34032451 DOI: 10.1021/acs.orglett.1c01375  0.353
2021 Cerveri A, Giovanelli R, Sella D, Pedrazzani R, Monari M, Nieto Faza O, López CS, Bandini M. Enantioselective CO Fixation Via a Heck-Coupling/Carboxylation Cascade Catalyzed by Nickel. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 33829576 DOI: 10.1002/chem.202101082  0.375
2020 An J, Pedrazzani R, Monari M, Marin-Luna M, Lopez CS, Bandini M. Site-selective synthesis of 1,3-dioxin-3-ones via a gold(i) catalyzed cascade reaction. Chemical Communications (Cambridge, England). PMID 32582892 DOI: 10.1039/D0Cc02703K  0.494
2020 Bandini M, Lombardi L, Bellini D, Bottoni A, Calvaresi M, Monari M, Kotvun A, Palermo V, Melucci M. Allylic and Allenylic Dearomatization of Indoles promoted by Graphene Oxide via Covalent Grafting Activation Mode. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 32346922 DOI: 10.1002/Chem.202001373  0.367
2020 An J, Bandini M. Recent Advances in the Catalytic Dearomatization of Naphthols European Journal of Organic Chemistry. 2020: 4087-4097. DOI: 10.1002/Ejoc.202000107  0.342
2020 Cerveri A, Bandini M. Recent Advances in the Catalytic Functionalization of “Electrophilic” Indoles Chinese Journal of Chemistry. 38: 287-294. DOI: 10.1002/Cjoc.201900446  0.335
2019 Liu Y, Parodi A, Battaglioli S, Monari M, Protti S, Bandini M. Visible-Light-Driven Synthesis of 1,3,4-Trisubstituted Pyrroles from Aryl Azides. Organic Letters. PMID 31545617 DOI: 10.1021/Acs.Orglett.9B02731  0.441
2019 Parodi A, Battaglioli S, Liu Y, Monari M, Marín-Luna M, Silva-López C, Bandini M. Scandium catalysed stereoselective thio-allylation of allenyl-imidates. Chemical Communications (Cambridge, England). PMID 31342026 DOI: 10.1039/C9Cc04302K  0.438
2019 Cerveri A, Faza ON, López CS, Grilli S, Monari M, Bandini M. Phosphine-Catalyzed Stereoselective Dearomatization of 3-NO-Indoles with Allenoates. The Journal of Organic Chemistry. PMID 31009560 DOI: 10.1021/Acs.Joc.9B00559  0.457
2019 Liu Y, Bandini M. Nickel Catalyzed Functionalization of Allenes Chinese Journal of Chemistry. 37: 431-441. DOI: 10.1002/Cjoc.201800568  0.359
2018 An J, Lombardi L, Grilli S, Bandini M. PPhAuTFA Catalyzed in the Dearomatization of 2-Naphthols with Allenamides. Organic Letters. PMID 30417649 DOI: 10.1021/Acs.Orglett.8B03018  0.532
2018 An J, Bandini M. Gold-catalyzed Dearomatization Reactions. Chimia. 72: 610-613. PMID 30257736 DOI: 10.2533/Chimia.2018.610  0.433
2018 Favaretto L, An J, Sambo M, De Nisi A, Bettini C, Melucci M, Kovtun A, Liscio A, Palermo V, Bottoni A, Zerbetto F, Calvaresi M, Bandini M. Graphene Oxide Promotes Site-Selective Allylic Alkylation of Thiophenes with Alcohols. Organic Letters. PMID 29863889 DOI: 10.1021/Acs.Orglett.8B01531  0.418
2018 Bandini M, Liu Y, Daka M. Regio- and Stereoselective Nickel-Catalyzed Coupling of Boronic Acids with Allenoates Synthesis. 50: 3187-3196. DOI: 10.1055/S-0037-1610023  0.408
2018 Liu Y, Cerveri A, De Nisi A, Monari M, Nieto Faza O, Lopez CS, Bandini M. Nickel catalyzed regio- and stereoselective arylation and methylation of allenamides via coupling reactions. An experimental and computational study Organic Chemistry Frontiers. 5: 3231-3239. DOI: 10.1039/C8Qo00729B  0.477
2018 Giacinto P, Bottoni A, Garelli A, Miscione GP, Bandini M. Covalent or Non-Covalent? A Mechanistic Insight into the Enantioselective Brønsted Acid Catalyzed Dearomatization of Indoles with Allenamides Chemcatchem. 10: 2442-2449. DOI: 10.1002/Cctc.201701933  0.422
2017 An J, Parodi A, Monari M, Reis MC, Lopez CS, Bandini M. Gold-Catalyzed Dearomatization of 2-Naphthols with Alkynes. Chemistry (Weinheim An Der Bergstrasse, Germany). 23: 17473-17477. PMID 29193515 DOI: 10.1002/Chem.201704942  0.483
2017 Liu Y, De Nisi A, Cerveri A, Monari M, Bandini M. Nickel-Catalyzed Synthesis of Stereochemically Defined Enamides via Bi- and Tricomponent Coupling Reaction. Organic Letters. 19: 5034-5037. PMID 28901140 DOI: 10.1021/Acs.Orglett.7B02166  0.529
2017 De Nisi A, Sierra S, Ferrara M, Monari M, Bandini M. TBAF catalyzed one-pot synthesis of allenyl-indoles Organic Chemistry Frontiers. 4: 1849-1853. DOI: 10.1039/C7Qo00414A  0.45
2017 Sauer C, Liu Y, De Nisi A, Protti S, Fagnoni M, Bandini M. Photocatalyst-free, Visible Light Driven, Gold Promoted Suzuki Synthesis of (Hetero)biaryls Chemcatchem. 9: 4456-4459. DOI: 10.1002/Cctc.201701436  0.465
2016 Manoni E, De Nisi A, Bandini M. New opportunities in the stereoselective dearomatization of indoles Pure and Applied Chemistry. 88: 207-214. DOI: 10.1515/Pac-2016-0101  0.501
2016 Manoni E, Bandini M. N-Allenyl Amides and O-Allenyl Ethers in Enantioselective Catalysis European Journal of Organic Chemistry. 2016: 3135-3142. DOI: 10.1002/Ejoc.201600304  0.397
2016 Quintavalla A, Bandini M. ChemInform Abstract: Gold-Catalyzed Allylation Reactions Cheminform. 47. DOI: 10.1002/chin.201624261  0.402
2016 Bandini M, Cera G, Miscione GP. Unveiling the Reaction Machinery of the [AuI]-Catalyzed Synthesis of Substituted Acenes by a [1,5]-H Shift Cascade Reaction Chemcatchem. 9: 316-321. DOI: 10.1002/Cctc.201601113  0.738
2016 Quintavalla A, Bandini M. Gold‐Catalyzed Allylation Reactions Chemcatchem. 8: 1437-1453. DOI: 10.1002/Cctc.201600071  0.504
2016 Manoni E, Daka M, Mastandrea MM, Nisi AD, Monari M, Bandini M. Catalytic α-Allylation of Enones with Alcohols via [Gold(I)]-Mediated [3,3]-Sigmatropic Rearrangement of Propargylic Carboxylates Advanced Synthesis & Catalysis. 358: 1404-1409. DOI: 10.1002/Adsc.201600113  0.5
2015 De Nisi A, Bergamini C, Leonzio M, Sartor G, Fato R, Naldi M, Monari M, Calonghi N, Bandini M. Synthesis, cytotoxicity and anti-cancer activity of new alkynyl-gold(i) complexes. Dalton Transactions (Cambridge, England : 2003). PMID 26687209 DOI: 10.1039/C5Dt02905H  0.318
2015 Ocello R, De Nisi A, Jia M, Yang QQ, Monari M, Giacinto P, Bottoni A, Miscione GP, Bandini M. Gold(I)-Catalyzed Dearomative [2+2]-Cycloaddition of Indoles with Activated Allenes: A Combined Experimental-Computational Study. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26517191 DOI: 10.1002/Chem.201503598  0.494
2015 Yang QQ, Marchini M, Xiao WJ, Ceroni P, Bandini M. Visible-Light-Induced Direct Photocatalytic Carboxylation of Indoles with CBr4 /MeOH. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26509744 DOI: 10.1002/Chem.201503787  0.459
2015 Mastandrea MM, Mellonie N, Giacinto P, Collado A, Nolan SP, Miscione GP, Bottoni A, Bandini M. Gold(I)-Assisted α-Allylation of Enals and Enones with Alcohols. Angewandte Chemie (International Ed. in English). PMID 26473619 DOI: 10.1002/Anie.201507218  0.452
2015 Jia M, Monari M, Yang QQ, Bandini M. Enantioselective gold catalyzed dearomative [2+2]-cycloaddition between indoles and allenamides. Chemical Communications (Cambridge, England). 51: 2320-3. PMID 25562811 DOI: 10.1039/C4Cc08736D  0.567
2015 Manoni E, Gualandi A, Mengozzi L, Bandini M, Cozzi PG. Organocatalytic enantioselective synthesis of 1-vinyl tetrahydroisoquinolines through allenamide activation with chiral Brønsted acids Rsc Advances. 5: 10546-10550. DOI: 10.1039/C4Ra14942D  0.68
2015 Jia M, Bandini M. Counterion effects in homogeneous gold catalysis Acs Catalysis. 5: 1638-1652. DOI: 10.1021/Cs501902V  0.457
2015 Rocchigiani L, Jia M, Bandini M, Macchioni A. Assessing the Role of Counterion in Gold-Catalyzed Dearomatization of Indoles with Allenamides by NMR Studies Acs Catalysis. 5: 3911-3915. DOI: 10.1021/Acscatal.5B00502  0.368
2015 Giacinto P, Cera G, Bottoni A, Bandini M, Miscione GP. DFT Mechanistic Investigation of the Gold(I)-Catalyzed Synthesis of Azepino[1,2-a]indoles Chemcatchem. 7: 2480-2484. DOI: 10.1002/Cctc.201500429  0.762
2014 Romano C, Jia M, Monari M, Manoni E, Bandini M. Metal-free enantioselective electrophilic activation of allenamides: stereoselective dearomatization of indoles. Angewandte Chemie (International Ed. in English). 53: 13854-7. PMID 25346494 DOI: 10.1002/Anie.201407518  0.488
2014 Jia M, Cera G, Perrotta D, Monari M, Bandini M. Taming gold(I)-counterion interplay in the de-aromatization of indoles with allenamides. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 9875-8. PMID 25044346 DOI: 10.1002/Chem.201403155  0.727
2014 Marchi E, Locritani M, Baroncini M, Bergamini G, Sinisi R, Monari M, Botta C, Mróz W, Bandini M, Ceroni P, Balzani V. Blue and highly emitting [Ir(iv)] complexes by an efficient photoreaction of yellow luminescent [Ir(iii)] complexes Journal of Materials Chemistry C. 2: 4461-4467. DOI: 10.1039/C4Tc00278D  0.363
2013 Chiarucci M, Bandini M. New developments in gold-catalyzed manipulation of inactivated alkenes. Beilstein Journal of Organic Chemistry. 9: 2586-614. PMID 24367423 DOI: 10.3762/Bjoc.9.294  0.379
2013 Chiarucci M, Mocci R, Syntrivanis LD, Cera G, Mazzanti A, Bandini M. Merging synthesis and enantioselective functionalization of indoles by a gold-catalyzed asymmetric cascade reaction. Angewandte Chemie (International Ed. in English). 52: 10850-3. PMID 24038961 DOI: 10.1002/Anie.201304619  0.784
2013 Chiarucci M, Matteucci E, Cera G, Fabrizi G, Bandini M. New entry to polycyclic fused indoles via gold(I)-catalyzed cascade reaction. Chemistry, An Asian Journal. 8: 1776-9. PMID 23894108 DOI: 10.1002/Asia.201201249  0.755
2013 Bandini M. Electrophilicity: the "dark-side" of indole chemistry. Organic & Biomolecular Chemistry. 11: 5206-12. PMID 23824171 DOI: 10.1039/C3Ob40735G  0.358
2013 Cera G, Bandini M. Enantioselective gold(I) catalysis with chiral monodentate ligands Israel Journal of Chemistry. 53: 848-855. DOI: 10.1002/Ijch.201300029  0.758
2013 Bandini M. ChemInform Abstract: Electrophilicity: The “Dark-Side” of Indole Chemistry Cheminform. 44: no-no. DOI: 10.1002/chin.201342227  0.309
2013 Cera G, Piscitelli S, Chiarucci M, Fabrizi G, Goggiamani A, Ramon RS, Nolan SP, Bandini M. ChemInform Abstract: One-Pot Gold-Catalyzed Synthesis of Azepino[1,2-a]indoles. Cheminform. 44: no-no. DOI: 10.1002/chin.201309167  0.4
2013 Cera G, Chiarucci M, Dosi F, Bandini M. Gold(I)-catalyzed functionalization of benzhydryl C (sp3)-H bonds Advanced Synthesis and Catalysis. 355: 2227-2231. DOI: 10.1002/Adsc.201300525  0.663
2012 Bandini M, Bottoni A, Chiarucci M, Cera G, Miscione GP. Mechanistic insights into enantioselective gold-catalyzed allylation of indoles with alcohols: the counterion effect. Journal of the American Chemical Society. 134: 20690-700. PMID 23193975 DOI: 10.1021/Ja3086774  0.755
2012 Cera G, Piscitelli S, Chiarucci M, Fabrizi G, Goggiamani A, Ramón RS, Nolan SP, Bandini M. One-pot gold-catalyzed synthesis of azepino[1,2-a]indoles. Angewandte Chemie (International Ed. in English). 51: 9891-5. PMID 22945878 DOI: 10.1002/Anie.201205463  0.788
2012 Cera G, Chiarucci M, Mazzanti A, Mancinelli M, Bandini M. Enantioselective gold-catalyzed synthesis of polycyclic indolines. Organic Letters. 14: 1350-3. PMID 22335367 DOI: 10.1021/Ol300297T  0.784
2012 Cera G, Chiarucci M, Bandini M. Accessing chemical diversity by stereoselective gold-catalyzed manipulation of allylic and propargylic alcohols Pure and Applied Chemistry. 84: 1673-1684. DOI: 10.1351/Pac-Con-11-09-05  0.727
2012 Chiarucci M, Di Lillo M, Romaniello A, Cozzi PG, Cera G, Bandini M. Gold meets enamine catalysis in the enantioselective α-allylic alkylation of aldehydes with alcohols Chemical Science. 3: 2859-2863. DOI: 10.1039/C2Sc20478A  0.785
2012 Bandini M, Cera G, Chiarucci M. ChemInform Abstract: The “Golden Age” of Gold Catalysis in Organic Synthesis Cheminform. 43: no-no. DOI: 10.1002/chin.201252184  0.685
2011 Chiarucci M, Locritani M, Cera G, Bandini M. Gold(I)-catalyzed synthesis of γ-vinylbutyrolactones by intramolecular oxaallylic alkylation with alcohols. Beilstein Journal of Organic Chemistry. 7: 1198-204. PMID 21977203 DOI: 10.3762/Bjoc.7.139  0.773
2011 Cera G, Crispino P, Monari M, Bandini M. Stereoselective synthesis of tetracyclic indolines via gold-catalyzed cascade cyclization reactions. Chemical Communications (Cambridge, England). 47: 7803-5. PMID 21633749 DOI: 10.1039/C1Cc12328A  0.762
2011 Bandini M. Allylic alcohols: sustainable sources for catalytic enantioselective alkylation reactions. Angewandte Chemie (International Ed. in English). 50: 994-5. PMID 21268189 DOI: 10.1002/Anie.201006522  0.469
2011 Bandini M. Gold-catalyzed decorations of arenes and heteroarenes with C-C multiple bonds. Chemical Society Reviews. 40: 1358-67. PMID 21103507 DOI: 10.1039/C0Cs00041H  0.393
2011 Bandini M, Gualandi A, Monari M, Romaniello A, Savoia D, Tragni M. Allylic alcohols: Valuable synthetic equivalents of non-activated alkenes in gold-catalyzed enantioselective alkylation of indoles Journal of Organometallic Chemistry. 696: 338-347. DOI: 10.1016/J.Jorganchem.2010.09.065  0.532
2010 Bandini M, Monari M, Romaniello A, Tragni M. Gold-catalyzed direct activation of allylic alcohols in the stereoselective synthesis of functionalized 2-vinyl-morpholines. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 14272-7. PMID 21089041 DOI: 10.1002/Chem.201002606  0.432
2010 Bandini M, Bottoni A, Eichholzer A, Miscione GP, Stenta M. Asymmetric phase-transfer-catalyzed intramolecular N-alkylation of indoles and pyrroles: a combined experimental and theoretical investigation. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 12462-73. PMID 20839181 DOI: 10.1002/Chem.201000560  0.469
2010 Bandini M, Bianchi M, Valenti G, Piccinelli F, Paolucci F, Monari M, Umani-Ronchi A, Marcaccio M. Electrochemiluminescent functionalizable cyclometalated thiophene-based iridium(III) complexes. Inorganic Chemistry. 49: 1439-48. PMID 20073514 DOI: 10.1021/Ic901660M  0.698
2010 Bandini M. Advances in Friedel−Crafts Acylation Reactions: Catalytic and Green Processes Advances in Friedel−Crafts Acylation Reactions: Catalytic and Green Processes . By Giovanni Sartori and Raimondo Maggi (both at University of Parma, Italy). CRC Press (an imprint of the Taylor & Francis Group): Boca Raton, FL. 2009. xii + 209 pp. $149.95. ISBN 978-1-4200-6792-7 . Journal of the American Chemical Society. 132: 7821-7822. DOI: 10.1021/Ja103390G  0.383
2010 Bandini M. ChemInform Abstract: General Aspects and Historical Background (Friedel-Crafts Alkylation Reactions) Cheminform. 41: no-no. DOI: 10.1002/chin.201025259  0.341
2010 Bandini M, Cozzi PG, Giacomini M, Melchiorre P, Selva S, Umani-Ronchi A. ChemInform Abstract: Sequential One-Pot InBr3-Catalyzed 1,4- then 1,2-Nucleophilic Addition to Enones. Cheminform. 33: no-no. DOI: 10.1002/chin.200244044  0.841
2010 Bandini M, Eichholzer A, Gualandi A, Quinto T, Savoia D. Creating chemical diversity in indole compounds by merging au and ru catalysis Chemcatchem. 2: 661-665. DOI: 10.1002/Cctc.201000077  0.523
2009 Bandini M, Eichholzer A. Catalytic functionalization of indoles in a new dimension. Angewandte Chemie (International Ed. in English). 48: 9608-44. PMID 19946913 DOI: 10.1002/Anie.200901843  0.406
2009 Bandini M, Eichholzer A. Enantioselective gold-catalyzed allylic alkylation of indoles with alcohols: an efficient route to functionalized tetrahydrocarbazoles. Angewandte Chemie (International Ed. in English). 48: 9533-7. PMID 19904785 DOI: 10.1002/Anie.200904388  0.443
2009 Bandini M, Sinisi R. Efficient guanidine-catalyzed alkylation of indoles with fluoromethyl ketones in the presence of water. Organic Letters. 11: 2093-6. PMID 19364115 DOI: 10.1021/Ol9005079  0.503
2009 Bandini M, Tragni M. Pi-activated alcohols: an emerging class of alkylating agents for catalytic Friedel-Crafts reactions. Organic & Biomolecular Chemistry. 7: 1501-7. PMID 19343234 DOI: 10.1039/B823217B  0.425
2009 Bandini M, Cabiddu S, Cadoni E, Olivelli P, Sinisi R, Umani-Ronchi A, Usai M. New adaptive chiral thiophene ligands for copper-catalyzed asymmetric Henry reaction. Chirality. 21: 239-44. PMID 18830973 DOI: 10.1002/chir.20613  0.759
2009 Bandini M, Pietrangelo A, Sinisi R, Umani-Ronchi A, Wolf MO. New electrochemlcally generated polymeric pd complexes as heterogeneous catalysts for Suzuki cross-coupling reactions European Journal of Organic Chemistry. 3554-3561. DOI: 10.1002/Ejoc.200900306  0.767
2009 Bandini M, Tragni M, Umani-Ronchi A. Iron (III)-catalyzed intramolecular friedel-crafts alkylation of electron-deficient arenes with π-activated alcohols Advanced Synthesis and Catalysis. 351: 2521-2524. DOI: 10.1002/Adsc.200900441  0.721
2009 Bandini M, Eichholzer A, Kotrusz P, Tragni M, Troisi S, Umani-Ronchi A. Ligand-free silver(I)-catalyzed intramolecular friedel-crafts alkylation of arenes with allylic alcohols Advanced Synthesis and Catalysis. 351: 319-324. DOI: 10.1002/Adsc.200800628  0.755
2009 Bandini M, Cozzi PG. Nucleophilic Substitution on Csp3 Carbon Atoms Catalytic Asymmetric Friedel-Crafts Alkylations. 167-202. DOI: 10.1002/9783527626977.ch5  0.469
2009 Bandini M, Umani-Ronchi A. Nucleophilic Allylic Alkylation and Hydroarylation of Allenes Catalytic Asymmetric Friedel-Crafts Alkylations. 145-166. DOI: 10.1002/9783527626977.ch4  0.772
2009 Bandini M, Umani-Ronchi A. Preface Catalytic Asymmetric Friedel-Crafts Alkylations. xiii-xiv. DOI: 10.1002/9783527626977  0.603
2008 Bandini M, Sinisi R, Umani-Ronchi A. Enantioselective organocatalyzed Henry reaction with fluoromethyl ketones. Chemical Communications (Cambridge, England). 4360-2. PMID 18802570 DOI: 10.1039/B807640E  0.782
2008 Bandini M, Eichholzer A, Tragni M, Umani-Ronchi A. Enantioselective phase-transfer-catalyzed intramolecular aza-Michael reaction: effective route to pyrazino-indole compounds. Angewandte Chemie (International Ed. in English). 47: 3238-41. PMID 18348111 DOI: 10.1002/Anie.200705685  0.75
2008 Bandini M, Contento M, Garelli A, Monari M, Tolomelli A, Umani-Ronchi A, Andriolo E, Montorsi M. A nonclassical stereoselective semi-synthesis of drospirenone via cross-metathesis reaction Synthesis. 3801-3804. DOI: 10.1055/S-0028-1087226  0.756
2008 Bandini M, Eichholzer A, Kotrusz P, Umani-Ronchi A. Highly efficient molybdenum(II)-catalyzed intramolecular allylic alkylation of arenes Advanced Synthesis and Catalysis. 350: 531-536. DOI: 10.1002/Adsc.200700607  0.762
2007 Bandini M, Melucci M, Piccinelli F, Sinisi R, Tommasi S, Umani-Ronchi A. New chiral diamino-bis(tert-thiophene): an effective ligand for Pd- and Zn-catalyzed asymmetric transformations. Chemical Communications (Cambridge, England). 4519-21. PMID 17971975 DOI: 10.1039/B711666G  0.748
2007 Bandini M, Benaglia M, Sinisi R, Tommasi S, Umani-Ronchi A. Recoverable PEG-supported copper catalyst for highly stereocontrolled nitroaldol condensation. Organic Letters. 9: 2151-3. PMID 17480085 DOI: 10.1021/Ol070636W  0.743
2007 Bandini M, Piccinelli F, Tommasi S, Umani-Ronchi A, Ventrici C. Highly enantioselective nitroaldol reaction catalyzed by new chiral copper complexes. Chemical Communications (Cambridge, England). 616-8. PMID 17264909 DOI: 10.1039/B613019D  0.799
2007 Bandini M. An update on catalytic enantioselective alkylations of indoles Mini-Reviews in Organic Chemistry. 4: 115-124. DOI: 10.2174/157019307780599270  0.47
2007 Bandini M, Umani-Ronchi A, Piccinelli F, Tommasi S, Ventrici C. Copper-Diamino Oligothiophene Catalyzed Henry Reaction Synfacts. 2007: 0410-0410. DOI: 10.1055/s-2007-968382  0.339
2007 Bandini M, Eichholzer A, Tommasi S, Umani-Ronchi A. Practical aspects in the gram-scale synthesis of chiral diamino-bithiophene 'DAT2' ligand Synthesis. 1587-1588. DOI: 10.1055/s-2007-965953  0.703
2007 Albano VG, Bandini M, Moorlag C, Piccinelli F, Pietrangelo A, Tommasi S, Umani-Ronchi A, Wolf MO. Electropolymerized Pd-containing thiophene polymer: A reusable supported catalyst for cross-coupling reactions Organometallics. 26: 4373-4375. DOI: 10.1021/Om070210L  0.74
2007 Sgreccia L, Bandini M, Morganti S, Quintavalla A, Umani-Ronchi A, Cozzi PG. Titanium-catalyzed Reformatsky-type reaction Journal of Organometallic Chemistry. 692: 3191-3197. DOI: 10.1016/J.Jorganchem.2007.02.037  0.806
2007 Giulio Albano V, Bandini M, Monari M, Piccinelli F, Tommasi S, Umani-Ronchi A. Synthesis, structural characterization, and catalytic activity of chiral diamine and diimine Pd(II)-complexes Inorganica Chimica Acta. 360: 1000-1008. DOI: 10.1016/J.Ica.2006.07.096  0.746
2007 Bandini M, Eichholzer A, Monari M, Piccinelli F, Umani-Ronchi A. Versatile base-catalyzed route to polycyclic heteroaromatic compounds by intramolecular Aza-Michael addition European Journal of Organic Chemistry. 2917-2920. DOI: 10.1002/ejoc.200601139  0.714
2007 Bandini M, Eichholzer A, Umani-Ronchi A. Catalytic Enantioselective Alkylation of Indoles Cheminform. 38. DOI: 10.1002/chin.200730248  0.784
2006 Angeli M, Bandini M, Garelli A, Piccinelli F, Tommasi S, Umani-Ronchi A. A practical synthetic route to functionalized THBCs and oxygenated analogues via intramolecular Friedel-Crafts reactions. Organic & Biomolecular Chemistry. 4: 3291-6. PMID 17036117 DOI: 10.1039/B607864H  0.791
2006 Melucci M, Barbarella G, Gazzano M, Cavallini M, Biscarini F, Bongini A, Piccinelli F, Monari M, Bandini M, Umani-Ronchi A, Biscarini P. Synthesis, multiphase characterization, and helicity control in chiral DACH-linked oligothiophenes. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 7305-12. PMID 16944542 DOI: 10.1002/Chem.200600312  0.694
2006 Albano VG, Bandini M, Monari M, Marcucci E, Piccinelli F, Umani-Ronchi A. Synthesis and crystallographic characterization of chiral bis-oxazoline-amides. Fine-tunable ligands for Pd-catalyzed asymmetric alkylations. The Journal of Organic Chemistry. 71: 6451-8. PMID 16901130 DOI: 10.1021/Jo060767V  0.745
2006 Bandini M, Melloni A, Piccinelli F, Sinisi R, Tommasi S, Umani-Ronchi A. Highly enantioselective synthesis of tetrahydro-beta-carbolines and tetrahydro-gamma-carbolines via Pd-catalyzed intramolecular allylic alkylation. Journal of the American Chemical Society. 128: 1424-5. PMID 16448093 DOI: 10.1021/Ja054109O  0.747
2006 Albano VG, Bandini M, Barbarella G, Melucci M, Monari M, Piccinelli F, Tommasi S, Umani-Ronchi A. Controlling stereochemical outcomes of asymmetric processes by catalyst remote molecular functionalizations: chiral diamino-oligothiophenes (DATs) as ligands in asymmetric catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). 12: 667-75. PMID 16283690 DOI: 10.1002/chem.200500889  0.751
2006 Bandini M, Benaglia M, Quinto T, Tommasi S, Umani-Ronchi A. PEG-Supported Chiral Diamine Ligand for Pd-Catalyzed Allylic Alkylation Synfacts. 2006: 1182-1182. DOI: 10.1055/s-2006-949410  0.713
2006 Bandini M, Bottoni A, Cozzi PG, Miscione GP, Monari M, Pierciaccante R, Umani-Ronchi A. Chiral C2-boron-bis(oxazolines) in asymmetric catalysis - A theoretical study of the catalyzed enantioselective reduction of ketones promoted by catecholborane European Journal of Organic Chemistry. 4596-4608. DOI: 10.1002/Ejoc.200600133  0.823
2006 Bandini M, Emer E, Tommasi S, Umani-Ronchi A. Innovative catalytic protocols for the ring-closing Friedel-crafts-type alkylation and alkenylation of arenes European Journal of Organic Chemistry. 3527-3544. DOI: 10.1002/Ejoc.200500995  0.829
2006 Bandini M, Benaglia M, Quinto T, Tommasi S, Umani-Ronchi A. New recoverable poly(ethylene glycol)-supported C1-diamino- oligothiophene ligands for palladium-promoted asymmetric allylic alkylation (AAA) reactions Advanced Synthesis and Catalysis. 348: 1521-1527. DOI: 10.1002/Adsc.200606125  0.783
2005 Bandini M, Garelli A, Rovinetti M, Tommasi S, Umani-Ronchi A. Catalytic enantioselective addition of indoles to arylnitroalkenes: an effective route to enantiomerically enriched tryptamine precursors. Chirality. 17: 522-9. PMID 16170793 DOI: 10.1002/chir.20189  0.792
2005 Bandini M, Melloni A, Tommasi S, Umani-Ronchi A. A journey across recent advances in catalytic and stereoselective alkylation of indoles Synlett. 1199-1222. DOI: 10.1055/S-2005-865210  0.782
2005 Albano VG, Bandini M, Melucci M, Monari M, Piccinelli F, Tommasi S, Umani-Ronchi A. Novel chiral diamino-oligothiophenes as valuable ligands in Pd-catalyzed allylic alkylations. On the "primary" role of "secondary" interactions in asymmetric catalysis Advanced Synthesis and Catalysis. 347: 1507-1512. DOI: 10.1002/adsc.200505109  0.719
2004 Bandini M, Fagioli M, Garavelli M, Melloni A, Trigari V, Umani-Ronchi A. Can simple enones be useful partners for the catalytic stereoselective alkylation of indoles? The Journal of Organic Chemistry. 69: 7511-8. PMID 15497976 DOI: 10.1021/jo0487202  0.764
2004 Bandini M, Melloni A, Umani-Ronchi A. New versatile Pd-catalyzed alkylation of indoles via nucleophilic allylic substitution: controlling the regioselectivity. Organic Letters. 6: 3199-202. PMID 15330622 DOI: 10.1021/Ol048663Z  0.772
2004 Bandini M, Melloni A, Umani-Ronchi A. New catalytic approaches in the stereoselective Friedel-Crafts alkylation reaction. Angewandte Chemie (International Ed. in English). 43: 550-6. PMID 14743405 DOI: 10.1002/Anie.200301679  0.791
2004 Bandini M, Cozzi PG, Melchiorre P, Umani-Ronchi A. Kinetic resolution of epoxides by a C-C bond-forming reaction: highly enantioselective addition of indoles to cis, trans, and meso aromatic epoxides catalyzed by [Cr(salen)] complexes. Angewandte Chemie (International Ed. in English). 43: 84-7. PMID 14694478 DOI: 10.1002/Anie.200352073  0.815
2004 Bandini M, Cozzi PG, Licciulli S, Umani-Ronchi A. A Cross Metathesis Based Protocol for the Effective Synthesis of Functionalised Allyl Bromides and Chlorides Synthesis. 409-414. DOI: 10.1055/S-2004-815936  0.831
2004 Bandini M, Fagioli M, Melloni A, Umani-Ronchi A. Polymer-supported indium lewis acid: Highly versatile catalyst for regio- and stereoselective ring-opening of epoxides Advanced Synthesis and Catalysis. 346: 573-578. DOI: 10.1002/Adsc.200303236  0.753
2004 Bandini M, Fagioli M, Umani-Ronchi A. Solid acid-catalysed michael-type conjugate addition of indoles to electron-poor C=C bonds: Towards high atom economical semicontinuous processes Advanced Synthesis and Catalysis. 346: 545-548. DOI: 10.1002/adsc.200303213  0.653
2003 Agnusdei M, Bandini M, Melloni A, Umani-Ronchi A. New versatile route to the synthesis of tetrahydro-beta-carbolines and tetrahydro-pyrano[3,4-b]indoles via an intramolecular Michael addition catalyzed by InBr3. The Journal of Organic Chemistry. 68: 7126-9. PMID 12946165 DOI: 10.1021/Jo034466M  0.747
2003 Bandini M, Fagioli M, Melloni A, Umani-Ronchi A. A general procedure for the synthesis of 1,3-bis(indolyl) compounds via Michael addition catalyzed by InBr3/TMSCl Synthesis. 397-402. DOI: 10.1055/S-2003-37359  0.763
2003 Bandini M, Fagioli M, Melchiorre P, Melloni A, Umani-Ronchi A. Catalytic enantioselective conjugate addition of indoles to simple α,β-unsaturated ketones Tetrahedron Letters. 44: 5843-5846. DOI: 10.1016/S0040-4039(03)01400-X  0.807
2003 Bandini M, Melloni A, Tominasi S, Umani-Ronchi A. Designing New α,β-Unsaturated Thioesters for the Catalytic, Enantioselective Friedel-Crafts Alkylation of Indoles Helvetica Chimica Acta. 86: 3753-3763. DOI: 10.1002/Hlca.200390317  0.748
2003 Bandini M, Bernardi F, Bottoni A, Cozzi PG, Miscione GP, Umani-Ronchi A. Bis(oxazoline)titanium complexes as chiral catalysts for enantioselective hydrosilylation of ketones - A combined experimental and theoretical investigation European Journal of Organic Chemistry. 2972-2984. DOI: 10.1002/Ejoc.200200675  0.816
2002 Bandini M, Cozzi PG, Melchiorre P, Umani-Ronchi A. InBr3-catalyzed Friedel-Crafts addition of indoles to chiral aromatic epoxides: a facile route to enantiopure indolyl derivatives. The Journal of Organic Chemistry. 67: 5386-9. PMID 12126434 DOI: 10.1021/Jo0256235  0.854
2002 Bandini M, Cozzi PG, Umani-Ronchi A. [Cr(Salen)] as a 'bridge' between asymmetric catalysis, Lewis acids and redox processes. Chemical Communications (Cambridge, England). 919-27. PMID 12123051 DOI: 10.1039/B109945K  0.807
2002 Bandini M, Cozzi PG, Giacomini M, Melchiorre P, Selva S, Umani-Ronchi A. Sequential one-pot InBr(3)-catalyzed 1,4- then 1,2-nucleophilic addition to enones. The Journal of Organic Chemistry. 67: 3700-4. PMID 12027683 DOI: 10.1021/Jo0163243  0.818
2002 Bandini M, Melchiorre P, Melloni A, Umani-Ronchi A. A practical indium tribromide catalysed addition of indoles to nitroalkenes in aqueous media Synthesis. 1110-1114. DOI: 10.1055/S-2002-31970  0.771
2002 Bandini M, Cozzi PG, Garelli A, Melchiorre P, Umani-Ronchi A. A convenient catalytic procedure for the addition of trimethylsilyl cyanide to functionalised ketones, mediated by InBr3 - Insight into the reaction mechanism European Journal of Organic Chemistry. 3243-3249. DOI: 10.1002/1099-0690(200210)2002:19<3243::Aid-Ejoc3243>3.0.Co;2-E  0.84
2001 Bandini M, Cozzi PG, Melchiorre P, Morganti S, Umani-Ronchi A. Cr(Salen)-catalyzed addition of 1,3-dichloropropene to aromatic aldehydes. A simple access to optically active vinyl epoxides. Organic Letters. 3: 1153-5. PMID 11348182 DOI: 10.1021/Ol015597H  0.847
2001 Bandini M, Cozzi PG, Umani-Ronchi A. Asymmetric synthesis with "privileged" ligands Pure and Applied Chemistry. 73: 325-329. DOI: 10.1351/Pac200173020325  0.832
2001 Bandini M, Cozzi PG, Monari M, Perciaccante R, Selva S, Umani-Ronchi A. Design of boron bis-oxazolinate (B-BOXate) complexes: A new class of stable organometallic catalysts Chemical Communications. 1318-1319. DOI: 10.1039/B103571C  0.789
2001 Bandini M, Cozzi PG, Melchiorre P, Tino R, Umani-Ronchi A. Chemo- and enantioselective catalytic addition of propargyl chloride to aldehydes promoted by [Cr(Salen)] complexes Tetrahedron Asymmetry. 12: 1063-1069. DOI: 10.1016/S0957-4166(01)00182-3  0.826
2001 Bandini M, Cozzi PG, Melchiorre P, Umani-Ronchi A. Indium tribromide: A highly effective catalyst for the addition of trimethylsilyl cyanide to α-hetero-substituted ketones Tetrahedron Letters. 42: 3041-3043. DOI: 10.1016/S0040-4039(01)00368-9  0.833
2001 Bandini M, Cozzi PG, Umani-Ronchi A. Enantioselective catalytic addition of allyl organometallic reagents to aldehydes promoted by [Cr(Salen)]: The hidden role played by weak Lewis acids in metallo-Salen promoted reactions Tetrahedron. 57: 835-843. DOI: 10.1016/S0040-4020(00)01047-4  0.799
2001 Bandini M, Cozzi PG, Gazzano M, Umani-Ronchi A. An effective and useful synthesis of enantiomerically enriched arylglycinols European Journal of Organic Chemistry. 1937-1942. DOI: 10.1002/1099-0690(200105)2001:10<1937::Aid-Ejoc1937>3.0.Co;2-2  0.803
2000 Bandini M, Cozzi PG, Umani-Ronchi A. Salen as a Chiral Activator: anti versus syn Switchable Diastereoselection in the Enantioselective Addition of Crotyl Bromide to Aromatic Aldehydes We thank the CNR (Rome), M.U.R.S.T. (Rome) "Progetto Stereoselezione in Chimica Organica, Metodologie ed Applicazioni", and the University of Bologna (funds for selected research topics) for financial support of this research. Angewandte Chemie (International Ed. in English). 39: 2327-2330. PMID 10941080 DOI: 10.1002/1521-3773(20000703)39:13<2327::Aid-Anie2327>3.0.Co;2-9  0.734
2000 Bandini M, Cozzi PG, Umani-Ronchi A. The first catalytic enantioselective Nozaki-Hiyama-Kishi reaction Polyhedron. 19: 537-539. DOI: 10.1016/S0277-5387(00)00290-4  0.83
2000 Bandini M, Cozzi PG, De Angelis M, Umani-Ronchi A. Zinc triflate-bis-oxazoline complexes as chiral catalysts: Enantioselective reduction of α-alkoxy-ketones with catecholborane Tetrahedron Letters. 41: 1601-1605. DOI: 10.1016/S0040-4039(99)02339-4  0.813
2000 Bandini M, Casolari S, Giorgio Cozzi P, Proni G, Schmohel E, Spada GP, Tagliavini E, Umani-Ronchi A. Synthesis and Characterization of New Enantiopure 7,7′-Disubstituted 2,2′-Dihydroxy-1,1′-binaphthyls: Useful Ligands for the Asymmetric Allylation Reaction of Aldehydes European Journal of Organic Chemistry. 2000: 491-497. DOI: 10.1002/(SICI)1099-0690(200002)2000:3<491::AID-EJOC491>3.0.CO;2-N  0.436
1999 Bandini M, Cozzi PG, Melchiorre P, Umani-Ronchi A. The First Catalytic Enantioselective Nozaki-Hiyama Reaction. Angewandte Chemie (International Ed. in English). 38: 3357-3359. PMID 10602193 DOI: 10.1002/(Sici)1521-3773(19991115)38:22<3357::Aid-Anie3357>3.0.Co;2-W  0.848
1999 Bandini M, Cozzi PG, Negro L, Umani-Ronchi A. Enantioselective reduction of ketones with triethoxysilane catalyzed by chiral bis-oxazoline titanium complexes Chemical Communications. 39-40. DOI: 10.1039/A807028H  0.817
1999 Bandini M, Cozzi PG, Morganti S, Umani-Ronchi A. Highly diastereoselective pinacol coupling of aldehydes catalyzed by titanium-schiff base complexes Tetrahedron Letters. 40: 1997-2000. DOI: 10.1016/S0040-4039(99)00100-8  0.801
1999 Bandini M, Cozzi PG, Umani-Ronchi A, Villa M. Diastereoselective addition of higher order cuprates and zinc-copper reagents to imines derived from (S)-1-phenylethylamine Tetrahedron. 55: 8103-8110. DOI: 10.1016/S0040-4020(99)00418-4  0.783
1999 Bandini M, Cozzi P, Melchiorre P, Umani-Ronchi A. Die erste katalytische enantioselektive Nozaki-Hiyama-Reaktion Angewandte Chemie. 111: 3558-3561. DOI: 10.1002/(Sici)1521-3757(19991115)111:22<3558::Aid-Ange3558>3.0.Co;2-6  0.616
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