| Year |
Citation |
Score |
| 2023 |
Paul S, Filippini D, Silvi M. Polarity Transduction Enables the Formal Electronically Mismatched Radical Addition to Alkenes. Journal of the American Chemical Society. PMID 36718934 DOI: 10.1021/jacs.2c12699 |
0.318 |
|
| 2021 |
Filippini D, Silvi M. Visible light-driven conjunctive olefination. Nature Chemistry. PMID 34737455 DOI: 10.1038/s41557-021-00807-x |
0.319 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Visible Light-Driven Strain-Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters. Angewandte Chemie (International Ed. in English). PMID 31912963 DOI: 10.1002/Anie.201915409 |
0.591 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Back Cover: Visible‐Light‐Driven Strain‐Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters (Angew. Chem. Int. Ed. 16/2020) Angewandte Chemie International Edition. 59: 6632-6632. DOI: 10.1002/Anie.202003607 |
0.537 |
|
| 2020 |
Davenport R, Silvi M, Noble A, Hosni Z, Fey N, Aggarwal VK. Rücktitelbild: Visible‐Light‐Driven Strain‐Increase Ring Contraction Allows the Synthesis of Cyclobutyl Boronic Esters (Angew. Chem. 16/2020) Angewandte Chemie. 132: 6694-6694. DOI: 10.1002/Ange.202003607 |
0.544 |
|
| 2019 |
Silvi M, Aggarwal VK. Radical Addition to Strained σ-Bonds Enables the Stereocontrolled Synthesis of Cyclobutyl Boronic Esters. Journal of the American Chemical Society. PMID 31142107 DOI: 10.1021/Jacs.9B03653 |
0.58 |
|
| 2018 |
Pelss A, Gandhamsetty N, Smith JR, Mailhol D, Silvi M, Watson A, Perez-Powell I, Prévost S, Schützenmeister N, Moore P, Aggarwal VK. Re-optimization of the Organocatalyzed Double Aldol Domino Process to a Key Enal Intermediate and its Application to the Total Synthesis of Δ¹²-Prostaglandin J₃. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29774967 DOI: 10.1002/Chem.201802498 |
0.556 |
|
| 2018 |
Silvi M, Schrof R, Noble A, Aggarwal VK. Enantiospecific Three-Component Alkylation of Furan and Indole. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29411914 DOI: 10.1002/Chem.201800527 |
0.577 |
|
| 2018 |
Silvi M, Melchiorre P. Enhancing the potential of enantioselective organocatalysis with light. Nature. 554: 41-49. PMID 29388950 DOI: 10.1038/Nature25175 |
0.594 |
|
| 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 |
0.636 |
|
| 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 |
0.647 |
|
| 2017 |
Silvi M, Sandford C, Aggarwal VK. Merging Photoredox with 1,2-Metallate Rearrangements: The Photochemical Alkylation of Vinyl Boronate Complexes. Journal of the American Chemical Society. PMID 28402109 DOI: 10.1021/Jacs.7B02569 |
0.596 |
|
| 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 |
0.671 |
|
| 2016 |
Garlets ZJ, Silvi M, Wolfe JP. Synthesis of Cyclic Guanidines via Silver-Catalyzed Intramolecular Alkene Hydroamination Reactions of N-Allylguanidines. Organic Letters. PMID 27181609 DOI: 10.1021/Acs.Orglett.6B00598 |
0.582 |
|
| 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 |
0.641 |
|
| 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 |
0.618 |
|
| 2013 |
Silvi M, Renzi P, Rosato D, Margarita C, Vecchioni A, Bordacchini I, Morra D, Nicolosi A, Cari R, Sciubba F, Scarpino Schietroma DM, Bella M. Enantioselective aza-Michael addition of imides by using an integrated strategy involving the synthesis of a family of multifunctional catalysts, usage of multiple catalysis, and rational design of experiment. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 9973-8. PMID 23765568 DOI: 10.1002/Chem.201301493 |
0.376 |
|
| 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 |
0.642 |
|
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