| Year |
Citation |
Score |
| 2024 |
Mallik S, Sfreddo E, Wang H, Melchiorre P. Radical pathways for 2,4-chromandione synthesis photoexcitation of 4-hydroxycoumarins. Chemical Science. 16: 124-129. PMID 39600514 DOI: 10.1039/d4sc07495e |
0.318 |
|
| 2024 |
Tseliou V, Kqiku L, Berger M, Schiel F, Zhou H, Poelarends GJ, Melchiorre P. Stereospecific radical coupling with a non-natural photodecarboxylase. Nature. 634: 848-854. PMID 39255850 DOI: 10.1038/s41586-024-08004-9 |
0.358 |
|
| 2024 |
Wu S, Melchiorre P. Photochemical Synthesis of Thioesters from Aryl Halides and Carboxylic Acids. Angewandte Chemie (International Ed. in English). e202407520. PMID 38887166 DOI: 10.1002/anie.202407520 |
0.365 |
|
| 2024 |
Wu S, Wong TH, Righi P, Melchiorre P. Photochemical Organocatalytic Synthesis of Thioethers from Aryl Chlorides and Alcohols. Journal of the American Chemical Society. PMID 38265336 DOI: 10.1021/jacs.3c13900 |
0.35 |
|
| 2023 |
Zhou W, Dmitriev IA, Melchiorre P. Reductive Cross-Coupling of Olefins via a Radical Pathway. Journal of the American Chemical Society. PMID 37947488 DOI: 10.1021/jacs.3c11285 |
0.32 |
|
| 2023 |
Balletti M, Wachsmuth T, Di Sabato A, Hartley WC, Melchiorre P. Enantioselective catalytic remote perfluoroalkylation of α-branched enals driven by light. Chemical Science. 14: 4923-4927. PMID 37181764 DOI: 10.1039/d3sc01347b |
0.353 |
|
| 2022 |
Georgiou E, Spinnato D, Chen K, Melchiorre P, Muñiz K. Switchable photocatalysis for the chemodivergent benzylation of 4-cyanopyridines. Chemical Science. 13: 8060-8064. PMID 35919417 DOI: 10.1039/d2sc02698h |
0.358 |
|
| 2022 |
Zhou W, Wu S, Melchiorre P. Tetrachlorophthalimides as Organocatalytic Acceptors for Electron Donor-Acceptor Complex Photoactivation. Journal of the American Chemical Society. PMID 35549337 DOI: 10.1021/jacs.2c03546 |
0.383 |
|
| 2022 |
Balletti M, Marcantonio E, Melchiorre P. Photochemical organocatalytic enantioselective radical γ-functionalization of α-branched enals. Chemical Communications (Cambridge, England). PMID 35481798 DOI: 10.1039/d2cc01638a |
0.408 |
|
| 2022 |
Hartley WC, Schiel F, Ermini E, Melchiorre P. Lewis Base-Catalysed Enantioselective Radical Conjugate Addition for the Synthesis of Enantioenriched Pyrrolidinones. Angewandte Chemie (International Ed. in English). e202204735. PMID 35452177 DOI: 10.1002/anie.202204735 |
0.429 |
|
| 2022 |
Wong TH, Ma D, Di Sanza R, Melchiorre P. Photoredox Organocatalysis for the Enantioselective Synthesis of 1,7-Dicarbonyl Compounds. Organic Letters. PMID 35199526 DOI: 10.1021/acs.orglett.2c00326 |
0.373 |
|
| 2022 |
Le Saux E, Zanini M, Melchiorre P. Photochemical Organocatalytic Benzylation of Allylic C-H Bonds. Journal of the American Chemical Society. PMID 35029387 DOI: 10.1021/jacs.1c11712 |
0.358 |
|
| 2021 |
Berger M, Carboni D, Melchiorre P. Photochemical Organocatalytic Regio- and Enantioselective Conjugate Addition of Allyl Groups to Enals. Angewandte Chemie (International Ed. in English). 60: 26373-26377. PMID 34695283 DOI: 10.1002/anie.202111648 |
0.398 |
|
| 2021 |
de Pedro Beato E, Spinnato D, Zhou W, Melchiorre P. A General Organocatalytic System for Electron Donor-Acceptor Complex Photoactivation and Its Use in Radical Processes. Journal of the American Chemical Society. PMID 34320312 DOI: 10.1021/jacs.1c05607 |
0.42 |
|
| 2021 |
Crisenza GEM, Faraone A, Gandolfo E, Mazzarella D, Melchiorre P. Catalytic asymmetric C-C cross-couplings enabled by photoexcitation. Nature Chemistry. 13: 575-580. PMID 34031564 DOI: 10.1038/s41557-021-00683-5 |
0.817 |
|
| 2021 |
Laroche B, Tang X, Archer G, Di Sanza R, Melchiorre P. Photochemical Chemoselective Alkylation of Tryptophan-Containing Peptides. Organic Letters. PMID 33400540 DOI: 10.1021/acs.orglett.0c03735 |
0.745 |
|
| 2020 |
Le Saux E, Ma D, Bonilla P, Holden C, Lustosa D, Melchiorre P. A General Organocatalytic System for Enantioselective Radical Conjugate Additions to Enals. Angewandte Chemie (International Ed. in English). PMID 33283919 DOI: 10.1002/anie.202014876 |
0.41 |
|
| 2020 |
de Pedro Beato E, Mazzarella D, Balletti M, Melchiorre P. Photochemical generation of acyl and carbamoyl radicals using a nucleophilic organic catalyst: applications and mechanism thereof. Chemical Science. 11: 6312-6324. PMID 32953026 DOI: 10.1039/D0Sc02313B |
0.814 |
|
| 2020 |
Crisenza GEM, Mazzarella D, Melchiorre P. Synthetic Methods Driven by the Photoactivity of Electron Donor-Acceptor Complexes. Journal of the American Chemical Society. PMID 32134647 DOI: 10.1021/Jacs.0C01416 |
0.776 |
|
| 2020 |
Melchiorre P, Spinnato D, Schweitzer-Chaput B, Goti G, Ošeka M. A Photochemical Organocatalytic Strategy for the α-Alkylation of Ketones using Radicals. Angewandte Chemie (International Ed. in English). PMID 32053279 DOI: 10.1002/Anie.201915814 |
0.518 |
|
| 2020 |
Alandini N, Buzzetti L, Favi G, Schulte T, Candish L, Collins K, Melchiorre P. Amide Synthesis by Nickel/Photoredox-Catalyzed Direct Carbamoylation of (Hetero)Aryl Bromides. Angewandte Chemie (International Ed. in English). PMID 32030865 DOI: 10.1002/Anie.202000224 |
0.495 |
|
| 2020 |
Crisenza GEM, Melchiorre P. Chemistry glows green with photoredox catalysis. Nature Communications. 11: 803. PMID 32029742 DOI: 10.1038/S41467-019-13887-8 |
0.319 |
|
| 2019 |
Gandolfo E, Tang X, Raha Roy S, Melchiorre P. Photochemical Asymmetric Nickel-Catalyzed Acyl Cross-Coupling. Angewandte Chemie (International Ed. in English). PMID 31532568 DOI: 10.1002/Anie.201910168 |
0.745 |
|
| 2019 |
Bieszczad B, Perego LA, Melchiorre P. Photochemical C-H Hydroxyalkylation of Quinolines and Isoquinolines. Angewandte Chemie (International Ed. in English). PMID 31529788 DOI: 10.1002/Anie.201910641 |
0.407 |
|
| 2019 |
Cuadros S, Horwitz MA, Schweitzer-Chaput B, Melchiorre P. A visible-light mediated three-component radical process using dithiocarbamate anion catalysis. Chemical Science. 10: 5484-5488. PMID 31293731 DOI: 10.1039/C9Sc00833K |
0.797 |
|
| 2019 |
van Leeuwen T, Buzzetti L, Perego LA, Melchiorre P. A Redox Active Nickel Complex that Acts as an Electron Mediator in Photochemical Giese Reactions. Angewandte Chemie (International Ed. in English). PMID 30747467 DOI: 10.1002/Anie.201814497 |
0.494 |
|
| 2019 |
Schweitzer-Chaput B, Horwitz MA, de Pedro Beato E, Melchiorre P. Photochemical generation of radicals from alkyl electrophiles using a nucleophilic organic catalyst. Nature Chemistry. 11: 129-135. PMID 30510217 DOI: 10.1038/S41557-018-0173-X |
0.809 |
|
| 2019 |
Mazzarella D, Magagnano G, Schweitzer-Chaput B, Melchiorre P. Photochemical Organocatalytic Borylation of Alkyl Chlorides, Bromides, and Sulfonates Acs Catalysis. 9: 5876-5880. DOI: 10.1021/Acscatal.9B01482 |
0.485 |
|
| 2019 |
Perego LA, Bonilla P, Melchiorre P. Photo‐Organocatalytic Enantioselective Radical Cascade Enabled by Single‐Electron Transfer Activation of Allenes Advanced Synthesis & Catalysis. 362: 302-307. DOI: 10.1002/Adsc.201900973 |
0.362 |
|
| 2018 |
Goti G, Bieszczad B, Vega-Peñaloza A, Melchiorre P. Stereocontrolled Synthesis of 1,4-Dicarbonyl Compounds by Photochemical Organocatalytic Acyl Radical Addition to Enals. Angewandte Chemie (International Ed. in English). PMID 30419156 DOI: 10.1002/Anie.201810798 |
0.499 |
|
| 2018 |
Buzzetti L, Crisenza GEM, Melchiorre P. Mechanistic Studies in Photocatalysis. Angewandte Chemie (International Ed. in English). PMID 30339746 DOI: 10.1002/Anie.201809984 |
0.346 |
|
| 2018 |
Cao ZY, Ghosh T, Melchiorre P. Enantioselective radical conjugate additions driven by a photoactive intramolecular iminium-ion-based EDA complex. Nature Communications. 9: 3274. PMID 30115906 DOI: 10.1038/S41467-018-05375-2 |
0.52 |
|
| 2018 |
Bonilla P, Rey Y, Holden C, Melchiorre P. Photo-Organocatalytic Enantioselective Radical Cascade Reactions of Unactivated Olefins. Angewandte Chemie (International Ed. in English). PMID 30098097 DOI: 10.1002/Anie.201808183 |
0.538 |
|
| 2018 |
Mazzarella D, Crisenza GEM, Melchiorre P. Asymmetric Photocatalytic C-H Functionalization of Toluene and Derivatives. Journal of the American Chemical Society. PMID 29932655 DOI: 10.1021/Jacs.8B05240 |
0.808 |
|
| 2018 |
Silvi M, Melchiorre P. Enhancing the potential of enantioselective organocatalysis with light. Nature. 554: 41-49. PMID 29388950 DOI: 10.1038/Nature25175 |
0.775 |
|
| 2018 |
Verrier C, Alandini N, Pezzetta C, Moliterno M, Buzzetti L, Hepburn HB, Vega-Peñaloza A, Silvi M, Melchiorre P. Direct Stereoselective Installation of Alkyl Fragments at the β-Carbon of Enals via Excited Iminium Ion Catalysis Acs Catalysis. 8: 1062-1066. DOI: 10.1021/Acscatal.7B03788 |
0.771 |
|
| 2017 |
Woźniak Ł, Magagnano G, Melchiorre P. Enantioselective Photochemical Organo-Cascade Catalysis. Angewandte Chemie (International Ed. in English). PMID 29205718 DOI: 10.1002/Anie.201711397 |
0.406 |
|
| 2017 |
Buzzetti L, Prieto A, Raha Roy S, Melchiorre P. Radical-based C-C Bond-Forming Processes Enabled by the Photoexcitation of 4-Alkyl-1,4-dihydropyridines. Angewandte Chemie (International Ed. in English). PMID 28984403 DOI: 10.1002/Anie.201709571 |
0.429 |
|
| 2017 |
Silvi M, Verrier C, Rey YP, Buzzetti L, Melchiorre P. Visible-light excitation of iminium ions enables the enantioselective catalytic β-alkylation of enals. Nature Chemistry. 9: 868-873. PMID 28837165 DOI: 10.1038/Nchem.2748 |
0.795 |
|
| 2017 |
Cuadros S, Dell'Amico L, Melchiorre P. Forging Quaternary Fluorine Stereocenters by a Light-driven Organocatalytic Aldol Desymmetrization Process. Angewandte Chemie (International Ed. in English). PMID 28746742 DOI: 10.1002/Anie.201706763 |
0.473 |
|
| 2017 |
Filippini G, Silvi M, Melchiorre P. Enantioselective Formal α-Methylation and α-Benzylation of Aldehydes by Means of Photo-Organocatalysis. Angewandte Chemie (International Ed. in English). PMID 28323367 DOI: 10.1002/Anie.201612045 |
0.793 |
|
| 2017 |
Bahamonde A, Murphy JJ, Savarese M, Bremond E, Cavalli A, Melchiorre P. Studies on the Enantioselective Iminium Ion Trapping of Radicals Triggered by an Electron-Relay Mechanism. Journal of the American Chemical Society. PMID 28281754 DOI: 10.1021/Jacs.7B01446 |
0.498 |
|
| 2017 |
Dell'Amico L, Fernández-Alvarez VM, Maseras F, Melchiorre P. Light-Driven Enantioselective Organocatalytic β-Benzylation of Enals. Angewandte Chemie (International Ed. in English). PMID 28185401 DOI: 10.1002/Anie.201612159 |
0.475 |
|
| 2016 |
Bahamonde A, Melchiorre P. On the Mechanism of the Stereoselective α-Alkylation of Aldehydes Driven by the Photochemical Activity of Enamines. Journal of the American Chemical Society. PMID 27267587 DOI: 10.1021/Jacs.6B04871 |
0.5 |
|
| 2016 |
Hepburn HB, Dell'Amico L, Melchiorre P. Enantioselective Vinylogous Organocascade Reactions. Chemical Record (New York, N.Y.). PMID 27256039 DOI: 10.1002/Tcr.201600030 |
0.477 |
|
| 2016 |
Murphy JJ, Bastida D, Paria S, Fagnoni M, Melchiorre P. Asymmetric catalytic formation of quaternary carbons by iminium ion trapping of radicals. Nature. 532: 218-22. PMID 27075098 DOI: 10.1038/Nature17438 |
0.47 |
|
| 2016 |
Hepburn HB, Melchiorre P. Brønsted acid-catalysed conjugate addition of photochemically generated α-amino radicals to alkenylpyridines. Chemical Communications (Cambridge, England). PMID 26839929 DOI: 10.1039/C5Cc10401G |
0.471 |
|
| 2016 |
Dell'Amico L, Vega-Peñaloza A, Cuadros S, Melchiorre P. Enantioselective Organocatalytic Diels-Alder Trapping of Photochemically Generated Hydroxy-o-Quinodimethanes. Angewandte Chemie (International Ed. in English). PMID 26797768 DOI: 10.1002/Anie.201509472 |
0.491 |
|
| 2016 |
Hepburn HB, Magagnano G, Melchiorre P. Light-Triggered Enantioselective Organocatalytic Mannich-Type Reaction Synthesis. 49: 76-86. DOI: 10.1055/S-0036-1588606 |
0.498 |
|
| 2015 |
Verrier C, Melchiorre P. Diastereodivergent organocatalysis for the asymmetric synthesis of chiral annulated furans. Chemical Science. 6: 4242-4246. PMID 29218190 DOI: 10.1039/C5Sc01052G |
0.457 |
|
| 2015 |
Murphy JJ, Melchiorre P. Organic chemistry: Light opens pathways for nickel catalysis. Nature. 524: 297-8. PMID 26266981 DOI: 10.1038/Nature15200 |
0.461 |
|
| 2015 |
Fernández-Alvarez VM, Nappi M, Melchiorre P, Maseras F. Computational study with DFT and kinetic models on the mechanism of photoinitiated aromatic perfluoroalkylations. Organic Letters. 17: 2676-9. PMID 25973535 DOI: 10.1021/Acs.Orglett.5B01069 |
0.369 |
|
| 2015 |
Wo?niak ?, Murphy JJ, Melchiorre P. Photo-organocatalytic Enantioselective Perfluoroalkylation of β-Ketoesters. Journal of the American Chemical Society. 137: 5678-81. PMID 25901659 DOI: 10.1021/Jacs.5B03243 |
0.427 |
|
| 2015 |
Silvi M, Arceo E, Jurberg ID, Cassani C, Melchiorre P. Enantioselective organocatalytic alkylation of aldehydes and enals driven by the direct photoexcitation of enamines. Journal of the American Chemical Society. 137: 6120-3. PMID 25748069 DOI: 10.1021/Jacs.5B01662 |
0.795 |
|
| 2015 |
Kandukuri SR, Bahamonde A, Chatterjee I, Jurberg ID, Escudero-Adán EC, Melchiorre P. X-ray characterization of an electron donor-acceptor complex that drives the photochemical alkylation of indoles. Angewandte Chemie (International Ed. in English). 54: 1485-9. PMID 25475488 DOI: 10.1002/Anie.201409529 |
0.774 |
|
| 2015 |
Filippini G, Nappi M, Melchiorre P. Photochemical direct perfluoroalkylation of phenols Tetrahedron. 71: 4535-4542. DOI: 10.1016/J.Tet.2015.02.034 |
0.378 |
|
| 2014 |
Arceo E, Montroni E, Melchiorre P. Photo-organocatalysis of atom-transfer radical additions to alkenes. Angewandte Chemie (International Ed. in English). 53: 12064-8. PMID 25243823 DOI: 10.1002/Anie.201406450 |
0.431 |
|
| 2014 |
Nappi M, Bergonzini G, Melchiorre P. Metal-free photochemical aromatic perfluoroalkylation of α-cyano arylacetates. Angewandte Chemie (International Ed. in English). 53: 4921-5. PMID 24668827 DOI: 10.1002/Anie.201402008 |
0.397 |
|
| 2014 |
Tian X, Hofmann N, Melchiorre P. Asymmetric vinylogous Diels-Alder reactions catalyzed by a chiral phosphoric acid. Angewandte Chemie (International Ed. in English). 53: 2997-3000. PMID 24504630 DOI: 10.1002/Anie.201310487 |
0.48 |
|
| 2014 |
List B, Pupo G, Arceo E, Montroni E, Melchiorre P. Organocatalytic Radical Addition to Alkenes Synfacts. 10: 1325-1325. DOI: 10.1055/S-0034-1379450 |
0.367 |
|
| 2014 |
Arceo E, Bahamonde A, Bergonzini G, Melchiorre P. Enantioselective direct α-alkylation of cyclic ketones by means of photo-organocatalysis Chemical Science. 5: 2438-2442. DOI: 10.1039/C4Sc00315B |
0.521 |
|
| 2014 |
CésardaSilva R, Chatterjee I, Escudero-Adán E, WeberPaixão M, Melchiorre P. Synthesis of cyclopropane spirooxindoles by means of a vinylogous organocatalytic cascade Asian Journal of Organic Chemistry. 3: 466-469. DOI: 10.1002/Ajoc.201400014 |
0.671 |
|
| 2013 |
Silvi M, Chatterjee I, Liu Y, Melchiorre P. Controlling the molecular topology of vinylogous iminium ions by logical substrate design: highly regio- and stereoselective aminocatalytic 1,6-addition to linear 2,4-dienals. Angewandte Chemie (International Ed. in English). 52: 10780-3. PMID 24038707 DOI: 10.1002/Anie.201305870 |
0.754 |
|
| 2013 |
Arceo E, Jurberg ID, Alvarez-Fernández A, Melchiorre P. Photochemical activity of a key donor-acceptor complex can drive stereoselective catalytic α-alkylation of aldehydes. Nature Chemistry. 5: 750-6. PMID 23965676 DOI: 10.1038/Nchem.1727 |
0.52 |
|
| 2013 |
Moran A, Hamilton A, Bo C, Melchiorre P. A mechanistic rationale for the 9-amino(9-deoxy)epi cinchona alkaloids catalyzed asymmetric reactions via iminium ion activation of enones. Journal of the American Chemical Society. 135: 9091-8. PMID 23746220 DOI: 10.1021/Ja404784T |
0.437 |
|
| 2013 |
Jurberg ID, Chatterjee I, Tannert R, Melchiorre P. When asymmetric aminocatalysis meets the vinylogy principle. Chemical Communications (Cambridge, England). 49: 4869-83. PMID 23598613 DOI: 10.1039/C3Cc41270A |
0.666 |
|
| 2013 |
Tian X, Melchiorre P. Control of remote stereochemistry in the synthesis of spirocyclic oxindoles: vinylogous organocascade catalysis. Angewandte Chemie (International Ed. in English). 52: 5360-3. PMID 23592417 DOI: 10.1002/Anie.201301017 |
0.331 |
|
| 2013 |
Cassani C, Martín-Rapún R, Arceo E, Bravo F, Melchiorre P. Synthesis of 9-amino(9-deoxy)epi cinchona alkaloids, general chiral organocatalysts for the stereoselective functionalization of carbonyl compounds. Nature Protocols. 8: 325-44. PMID 23329005 DOI: 10.1038/Nprot.2012.155 |
0.422 |
|
| 2013 |
Bastida D, Liu Y, Tian X, Escudero-Adán E, Melchiorre P. Asymmetric vinylogous aldol reaction via H-bond-directing dienamine catalysis. Organic Letters. 15: 220-3. PMID 23259650 DOI: 10.1021/Ol303312P |
0.44 |
|
| 2013 |
Moran A, Hamilton A, Bo C, Melchiorre P. Another Stereochemical Model for Cinchona-Derived Primary Amine Catalysts Synfacts. 9: 891-891. DOI: 10.1055/S-0033-1339446 |
0.343 |
|
| 2013 |
Chatterjee I, Bastida D, Melchiorre P. Vinylogous organocatalytic triple cascade reaction: Forging six stereocenters in complex spiro-oxindolic cyclohexanes Advanced Synthesis and Catalysis. 355: 3124-3130. DOI: 10.1002/Adsc.201300667 |
0.66 |
|
| 2012 |
Cassani C, Melchiorre P. Direct catalytic enantioselective vinylogous aldol reaction of α-branched enals with isatins. Organic Letters. 14: 5590-3. PMID 23075306 DOI: 10.1021/Ol302711W |
0.467 |
|
| 2012 |
Melchiorre P. Cinchona-based primary amine catalysis in the asymmetric functionalization of carbonyl compounds. Angewandte Chemie (International Ed. in English). 51: 9748-70. PMID 22893602 DOI: 10.1002/Anie.201109036 |
0.421 |
|
| 2012 |
Tian X, Liu Y, Melchiorre P. Aminocatalytic enantioselective 1,6 additions of alkyl thiols to cyclic dienones: vinylogous iminium ion activation. Angewandte Chemie (International Ed. in English). 51: 6439-42. PMID 22615236 DOI: 10.1002/Anie.201202392 |
0.456 |
|
| 2012 |
Liu Y, Nappi M, Escudero-Adán EC, Melchiorre P. Multicatalytic asymmetric synthesis of complex tetrahydrocarbazoles via a Diels-Alder/benzoin reaction sequence. Organic Letters. 14: 1310-3. PMID 22381336 DOI: 10.1021/Ol300192P |
0.434 |
|
| 2012 |
Retini M, Bergonzini G, Melchiorre P. Dioxindole in asymmetric catalytic synthesis: direct access to 3-substituted 3-hydroxy-2-oxindoles via 1,4-additions to nitroalkenes. Chemical Communications (Cambridge, England). 48: 3336-8. PMID 22362379 DOI: 10.1039/C2Cc30198A |
0.431 |
|
| 2012 |
Bergonzini G, Melchiorre P. Dioxindole in asymmetric catalytic synthesis: routes to enantioenriched 3-substituted 3-hydroxyoxindoles and the preparation of maremycin A. Angewandte Chemie (International Ed. in English). 51: 971-4. PMID 22173973 DOI: 10.1002/Anie.201107443 |
0.437 |
|
| 2012 |
Silvi M, Cassani C, Moran A, Melchiorre P. Secondary amine-catalyzed asymmetric γ-alkylation of α-branched enals via dienamine activation Helvetica Chimica Acta. 95: 1985-2006. DOI: 10.1002/Hlca.201200412 |
0.785 |
|
| 2011 |
Tian X, Cassani C, Liu Y, Moran A, Urakawa A, Galzerano P, Arceo E, Melchiorre P. Diastereodivergent asymmetric sulfa-Michael additions of α-branched enones using a single chiral organic catalyst. Journal of the American Chemical Society. 133: 17934-41. PMID 21936561 DOI: 10.1021/Ja207847P |
0.468 |
|
| 2011 |
Liu Y, Nappi M, Arceo E, Vera S, Melchiorre P. Asymmetric catalysis of Diels-Alder reactions with in situ generated heterocyclic ortho-quinodimethanes. Journal of the American Chemical Society. 133: 15212-8. PMID 21842900 DOI: 10.1021/Ja206517S |
0.496 |
|
| 2011 |
Cassani C, Tian X, Escudero-Adán EC, Melchiorre P. Multiple approaches to enantiopure spirocyclic benzofuranones using organocatalytic cascade reactions. Chemical Communications (Cambridge, England). 47: 233-5. PMID 20721390 DOI: 10.1039/C0Cc01957G |
0.403 |
|
| 2011 |
Vera S, Liu Y, Marigo M, Escudero-Adán EC, Melchiorre P. Asymmetric Michael addition of nitrobenzyl pyridines to enals via iminium catalysis Synlett. 489-494. DOI: 10.1055/S-0030-1259518 |
0.454 |
|
| 2011 |
Bergonzini G, Vera S, Melchiorre P. γ-Alkylation of α-Branched Enals with Stable Carbocations Synfacts. 2011: 101-101. DOI: 10.1055/S-0030-1259190 |
0.323 |
|
| 2010 |
Bergonzini G, Vera S, Melchiorre P. Cooperative organocatalysis for the asymmetric γ alkylation of α-branched enals. Angewandte Chemie (International Ed. in English). 49: 9685-8. PMID 21053229 DOI: 10.1002/Anie.201004761 |
0.346 |
|
| 2010 |
Bencivenni G, Galzerano P, Mazzanti A, Bartoli G, Melchiorre P. Direct asymmetric vinylogous Michael addition of cyclic enones to nitroalkenes via dienamine catalysis. Proceedings of the National Academy of Sciences of the United States of America. 107: 20642-7. PMID 20566884 DOI: 10.1073/Pnas.1001150107 |
0.483 |
|
| 2010 |
De Vincentiis F, Bencivenni G, Pesciaioli F, Mazzanti A, Bartoli G, Galzerano P, Melchiorre P. Asymmetric catalytic aziridination of cyclic enones. Chemistry, An Asian Journal. 5: 1652-6. PMID 20512797 DOI: 10.1002/Asia.201000040 |
0.441 |
|
| 2010 |
Galzerano P, Agostino D, Bencivenni G, Sambri L, Bartoli G, Melchiorre P. Controlling stereoselectivity in the aminocatalytic enantioselective Mannich reaction of aldehydes with in situ generated N-carbamoyl imines. Chemistry (Weinheim An Der Bergstrasse, Germany). 16: 6069-76. PMID 20397160 DOI: 10.1002/Chem.200903217 |
0.419 |
|
| 2010 |
Dalpozzo R, Bartoli G, Sambri L, Melchiorre P. Perchloric acid and its salts: very powerful catalysts in organic chemistry. Chemical Reviews. 110: 3501-51. PMID 20235581 DOI: 10.1021/Cr9003488 |
0.326 |
|
| 2010 |
Bencivenni G, Galzerano P, Mazzanti A, Bartoli G, Melchiorre P. Organocatalytic Vinylogous Michael Additions Synfacts. 2010: 1299-1299. DOI: 10.1055/S-0030-1258785 |
0.426 |
|
| 2010 |
Vincentiis Fd, Bencivenni G, Pesciaioli F, Mazzanti A, Bartoli G, Galzerano P, Melchiorre P. Aziridination of Cyclic Enones Synfacts. 2010: 949-949. DOI: 10.1055/S-0030-1257808 |
0.327 |
|
| 2010 |
Pesciaioli F, Tian X, Bencivenni G, Bartoli G, Melchiorre P. Organocatalytic asymmetric conjugate additions of oxindoles and benzofuranones to cyclic enones Synlett. 1704-1708. DOI: 10.1055/S-0029-1219955 |
0.457 |
|
| 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 |
0.699 |
|
| 2010 |
Marigo M, Melchiorre P. Chemoselectivity in asymmetric aminocatalysis Chemcatchem. 2: 621-623. DOI: 10.1002/Cctc.201000110 |
0.408 |
|
| 2010 |
Melchiorre P. Cinchona Alkaloids in Synthesis & Catalysis. Ligands, Immobilization and Organocatalysis. Edited by Choong Eui Song. Angewandte Chemie International Edition. 49: 3259-3260. DOI: 10.1002/Anie.201000372 |
0.337 |
|
| 2010 |
Melchiorre P. Cinchona Alkaloids in Synthesis & Catalysis. Ligands, Immobilization and Organocatalysis. Herausgegeben von Choong Eui Song. Angewandte Chemie. 122: 3329-3330. DOI: 10.1002/Ange.201000372 |
0.336 |
|
| 2009 |
Wu LY, Bencivenni G, Mancinelli M, Mazzanti A, Bartoli G, Melchiorre P. Organocascade reactions of enones catalyzed by a chiral primary amine. Angewandte Chemie (International Ed. in English). 48: 7196-9. PMID 19718738 DOI: 10.1002/Anie.200903280 |
0.45 |
|
| 2009 |
Cucinotta CS, Kosa M, Melchiorre P, Cavalli A, Gervasio FL. Bifunctional catalysis by natural cinchona alkaloids: a mechanism explained. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 7913-21. PMID 19492372 DOI: 10.1002/Chem.200900406 |
0.413 |
|
| 2009 |
Galzerano P, Bencivenni G, Pesciaioli F, Mazzanti A, Giannichi B, Sambri L, Bartoli G, Melchiorre P. Asymmetric iminium ion catalysis with a novel bifunctional primary amine thiourea: controlling adjacent quaternary and tertiary stereocenters. Chemistry (Weinheim An Der Bergstrasse, Germany). 15: 7846-9. PMID 19180604 DOI: 10.1002/Chem.200802466 |
0.328 |
|
| 2009 |
Melchiorre P. Light in aminocatalysis: the asymmetric intermolecular alpha-alkylation of aldehydes. Angewandte Chemie (International Ed. in English). 48: 1360-3. PMID 19132644 DOI: 10.1002/Anie.200804995 |
0.352 |
|
| 2009 |
Wu L-, Bencivenni G, Mancinelli M, Mazzanti A, Bartoli G, Melchiorre P. Aminocatalysis Cascades of Enones Synfacts. 2009: 1283-1283. DOI: 10.1055/S-0029-1218112 |
0.332 |
|
| 2009 |
Galzerano P, Pesciaioli F, Mazzanti A, Bartoli G, Melchiorre P. Asymmetric Organocatalytic Cascade Reactions with α‐Substituted α,β‐Unsaturated Aldehydes Angewandte Chemie. 48: 7892-7894. DOI: 10.1002/Ange.200903803 |
0.423 |
|
| 2009 |
García JM, Oiarbide M, Palomo C, Bartoli G, Melchiorre P, Bernardi L, Ricci A. Michael Addition Catalytic Asymmetric Friedel-Crafts Alkylations. 17-99. DOI: 10.1002/9783527626977.ch2 |
0.549 |
|
| 2008 |
Gianelli C, Sambri L, Carlone A, Bartoli G, Melchiorre P. Aminocatalytic enantioselective anti-Mannich reaction of aldehydes with in situ generated N-Cbz and N-Boc imines. Angewandte Chemie (International Ed. in English). 47: 8700-2. PMID 18846535 DOI: 10.1002/Anie.200803819 |
0.328 |
|
| 2008 |
Shaikh RR, Mazzanti A, Petrini M, Bartoli G, Melchiorre P. Proline-catalyzed asymmetric formal alpha-alkylation of aldehydes via vinylogous iminium ion intermediates generated from arylsulfonyl indoles. Angewandte Chemie (International Ed. in English). 47: 8707-10. PMID 18846525 DOI: 10.1002/Anie.200803947 |
0.37 |
|
| 2008 |
Pesciaioli F, De Vincentiis F, Galzerano P, Bencivenni G, Bartoli G, Mazzanti A, Melchiorre P. Organocatalytic asymmetric aziridination of enones. Angewandte Chemie (International Ed. in English). 47: 8703-6. PMID 18846523 DOI: 10.1002/Anie.200803647 |
0.421 |
|
| 2008 |
Melchiorre P, Marigo M, Carlone A, Bartoli G. Asymmetric aminocatalysis--gold rush in organic chemistry. Angewandte Chemie (International Ed. in English). 47: 6138-71. PMID 18666089 DOI: 10.1002/Anie.200705523 |
0.388 |
|
| 2008 |
Penon O, Carlone A, Mazzanti A, Locatelli M, Sambri L, Bartoli G, Melchiorre P. Quaternary stereogenic carbon atoms in complex molecules by an asymmetric, organocatalytic, triple-cascade reaction. Chemistry (Weinheim An Der Bergstrasse, Germany). 14: 4788-91. PMID 18412168 DOI: 10.1002/Chem.200800440 |
0.34 |
|
| 2008 |
Bartoli G, Melchiorre P. A novel organocatalytic tool for the iminium activation of α,β-unsaturated ketones Synlett. 1759-1772. DOI: 10.1055/S-2008-1078503 |
0.491 |
|
| 2008 |
Bartoli G, Bosco M, Carlone A, Dalpozzo R, Galzerano P, Melchiorre P, Sambri L. Magnesium perchlorate as efficient Lewis acid for the Knoevenagel condensation between β-diketones and aldehydes Tetrahedron Letters. 49: 2555-2557. DOI: 10.1016/J.Tetlet.2008.02.093 |
0.36 |
|
| 2008 |
Bartoli G, Bosco M, Galzerano P, Giri R, Mazzanti A, Melchiorre P, Sambri L. Multicomponent domino reaction promoted by Mg(ClO4)2: Highly efficient access to functionalized 1,4-dihydropyridines European Journal of Organic Chemistry. 3970-3975. DOI: 10.1002/Ejoc.200800422 |
0.435 |
|
| 2008 |
Ricci P, Carlone A, Bartoli G, Bosco M, Sambri L, Melchiorre P. Organocatalytic asymmetric sulfa-michael addition to α,β- unsaturated ketones Advanced Synthesis and Catalysis. 350: 49-53. DOI: 10.1002/Adsc.200700382 |
0.465 |
|
| 2007 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Mazzanti A, Sambri L, Melchiorre P. Organocatalytic asymmetric hydrophosphination of nitroalkenes. Chemical Communications (Cambridge, England). 722-4. PMID 17392962 DOI: 10.1039/B613477G |
0.37 |
|
| 2007 |
Bartoli G, Bosco M, Carlone A, Pesciaioli F, Sambri L, Melchiorre P. Organocatalytic asymmetric Friedel-Crafts alkylation of indoles with simple alpha,beta-unsaturated ketones. Organic Letters. 9: 1403-5. PMID 17346059 DOI: 10.1021/Ol070309O |
0.397 |
|
| 2007 |
Bartoli G, Babiuch K, Bosco M, Carlone A, Galzerano P, Melchiorre P, Sambri L. Magnesium perchlorate as efficient Lewis acid: A simple and convenient route to 1,4-dihydropyridines Synlett. 2897-2901. DOI: 10.1055/S-2007-990839 |
0.372 |
|
| 2007 |
Bartoli G, Bosco M, Carlone A, Dalpozzo R, Marcantoni E, Melchiorre P, Sambri L. Reaction of dicarbonates with carboxylic acids catalyzed by weak Lewis acids: General method for the synthesis of anhydrides and esters Synthesis. 3489-3496. DOI: 10.1055/S-2007-990812 |
0.368 |
|
| 2007 |
Melchiorre P, Carlone A, Bartoli G, Bosco M, Sambri L. Asymmetric Hydrophosphination of Enals Synfacts. 2007: 0760-0760. DOI: 10.1055/S-2007-968625 |
0.381 |
|
| 2007 |
Melchiorre P, Bartoli G, Bosco M, Carlone A, Pesciaioli F, Sambri L. Organocatalytic Asymmetric Friedel-Crafts Alkylation of Indoles with Enones Synfacts. 2007: 0542-0542. DOI: 10.1055/S-2007-968405 |
0.47 |
|
| 2007 |
Melchiorre P, Bartoli G, Bosco M, Carlone A, Locatelli M, Mazzanti A, Sambri L. Asymmetric Hydrophosphination of Nitroalkenes Synfacts. 2007: 0316-0316. DOI: 10.1055/S-2007-968237 |
0.381 |
|
| 2007 |
Carlone A, Bartoli G, Bosco M, Pesciaioli F, Ricci P, Sambri L, Melchiorre P. Organocatalytic asymmetric β-hydroxylation of α,β- unsaturated ketones European Journal of Organic Chemistry. 5492-5495. DOI: 10.1002/Ejoc.200700873 |
0.418 |
|
| 2007 |
Bartoli G, Locatelli M, Melchiorre P, Sambri L. Taking up the cudgels for perchlorates: Uses and applications in organic reactions under mild conditions European Journal of Organic Chemistry. 2037-2049. DOI: 10.1002/Ejoc.200600852 |
0.381 |
|
| 2006 |
Bartoli G, Bosco M, Carlone A, Dalpozzo R, Locatelli M, Melchiorre P, Sambri L. Alcohols and di-tert-butyl dicarbonate: how the nature of the Lewis acid catalyst may address the reaction to the synthesis of tert-butyl ethers. The Journal of Organic Chemistry. 71: 9580-8. PMID 17168573 DOI: 10.1021/Jo061402D |
0.438 |
|
| 2006 |
Bartoli G, Bosco M, Carlone A, Dalpozzo R, Locatelli M, Melchiorre P, Palazzi P, Sambri L. The first simple method of protection of hydroxy compounds as their O-Boc derivatives under Lewis acid catalysis Synlett. 2104-2108. DOI: 10.1055/S-2006-949609 |
0.399 |
|
| 2006 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Marcantoni E, Melchiorre P, Palazzi P, Sambri L. A new, mild, general and efficient route to aryl ethyl carbonates in solvent-free conditions promoted by magnesium perchlorate European Journal of Organic Chemistry. 4429-4434. DOI: 10.1002/Ejoc.200600366 |
0.439 |
|
| 2006 |
Bartoli G, Giovannini R, Giuliani A, Marcantoni E, Massaccesi M, Melchiorre P, Paoletti M, Sambri L. Solvent-free carbon-oxygen bond formation catalysed by CeCl 3·7H2O/NaI: Tetrahydropyranylation of hydroxy groups European Journal of Organic Chemistry. 1476-1482. DOI: 10.1002/Ejoc.200500780 |
0.455 |
|
| 2006 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Marcantoni E, Melchiorre P, Sambri L. tert-butyl ethers: Renaissance of an alcohol protecting group. Facile cleavage with cerium(III) chloride/sodium iodide Advanced Synthesis and Catalysis. 348: 905-910. DOI: 10.1002/Adsc.200505469 |
0.322 |
|
| 2005 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Melchiorre P, Sambri L. Direct catalytic synthesis of enantiopure 5-substituted oxazolidinones from racemic terminal epoxides. Organic Letters. 7: 1983-5. PMID 15876035 DOI: 10.1021/Ol050675C |
0.449 |
|
| 2005 |
Bartoli G, Bosco M, Locatelli M, Marcantoni E, Melchiorre P, Sambri L. Unusual and unexpected reactivity of t-butyl dicarbonate (Boc2O) with alcohols in the presence of magnesium perchlorate. A new and general route to t-butyl ethers. Organic Letters. 7: 427-30. PMID 15673256 DOI: 10.1021/Ol047704O |
0.348 |
|
| 2005 |
Bartoli G, Giuliani A, Marcantoni E, Massaccesi M, Melchiorre P, Lanari S, Sambri L. Allylation of aldehydes promoted by the cerium(III) chloride heptahydrate/sodium iodide system: The dependence of regio- and stereocontrol on the reaction conditions Advanced Synthesis and Catalysis. 347: 1673-1680. DOI: 10.1002/Adsc.200505184 |
0.451 |
|
| 2005 |
Bartoli G, Boeglin J, Bosco M, Locatelli M, Massaccesi M, Melchiorre P, Sambri L. Highly efficient solvent-free condensation of carboxylic acids with alcohols catalysed by zinc perchlorate hexahydrate, Zn(ClO4) 2·6 H2O Advanced Synthesis and Catalysis. 347: 33-38. DOI: 10.1002/Adsc.200404171 |
0.355 |
|
| 2004 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Melchiorre P, Sambri L. Asymmetric catalytic synthesis of enantiopure N-protected 1,2-amino alcohols. Organic Letters. 6: 3973-5. PMID 15496077 DOI: 10.1021/Ol048322L |
0.433 |
|
| 2004 |
Bartoli G, Bosco M, Carlone A, Locatelli M, Massaccesi M, Melchiorre P, Sambri L. Asymmetric aminolysis of aromatic epoxides: a facile catalytic enantioselective synthesis of anti-beta-amino alcohols. Organic Letters. 6: 2173-6. PMID 15200313 DOI: 10.1021/Ol049372T |
0.388 |
|
| 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 |
0.688 |
|
| 2004 |
Bartoli G, Bosco M, Locatelli M, Marcantoni E, Massaccesi M, Melchiorre P, Sambri L. A Lewis acid-mediated protocol for the protection of aryl amines as their Boc-derivatives Synlett. 1794-1798. DOI: 10.1055/S-2004-829059 |
0.363 |
|
| 2004 |
Bartoli G, Bosco M, Locatelli M, Marcantoni E, Melchiorre P, Sambri L. Zn(ClO4)2·6H2O as a Powerful Catalyst for the Conversion of β-Ketoesters into β-Enamino Esters Synlett. 239-242. DOI: 10.1055/S-2003-44974 |
0.332 |
|
| 2004 |
Bartoli G, Bosco M, Marcantoni E, Melchiorre P, Rinaldi S, Sambri L. Highly Stereoselective Reduction of β-Keto Amides: The First General and Efficient Approach to N-mono- and non-Substituted anti-α-Alkyl β-Hydroxy Amides Synlett. 73-76. DOI: 10.1055/S-2003-43354 |
0.381 |
|
| 2003 |
Melchiorre P, Jørgensen KA. Direct enantioselective Michael addition of aldehydes to vinyl ketones catalyzed by chiral amines. The Journal of Organic Chemistry. 68: 4151-7. PMID 12762713 DOI: 10.1021/Jo026837P |
0.632 |
|
| 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 |
0.717 |
|
| 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 |
0.738 |
|
| 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 |
0.695 |
|
| 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 |
0.68 |
|
| 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 |
0.727 |
|
| 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 |
0.727 |
|
| 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 |
0.69 |
|
| 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 |
0.719 |
|
| 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 |
0.724 |
|
| 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 |
0.417 |
|
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